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Disease on EC 1.14.19.1 - stearoyl-CoA 9-desaturase

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DISEASE
TITLE OF PUBLICATION
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Abnormalities, Multiple
12-lead electrocardiogram as a predictor of sudden cardiac death: from epidemiology to clinical practice.
Abortion, Spontaneous
A novel non-invasive prenatal sickle cell disease test for all at-risk pregnancies.
[Correlation of the DNA fragmentation index and malformation rate of optimized sperm with embryonic development and early spontaneous abortion in IVF-ET].
Abruptio Placentae
Perinatal implications of sickle cell disease.
Abscess
Application of suction-type cigarette drain in leak-prone hepatopancreatobiliary surgery.
Salmonella enteritidis brain abscess in a sickle cell disease patient: case report and review of the literature.
Splenectomy for hematological diseases: The Qatif Central Hospital experience.
Splenectomy in patients with sickle-cell disease.
Splenic abscess and sickle cell disease.
Splenic sepsis in sickle cell disease.
Acidosis
Do we have to consider acidosis induced by exercise as deleterious in sickle cell disease?
Endurance training reduces exercise-induced acidosis and improves muscle function in a mouse model of sickle cell disease.
Hematopoietic cell transplantation for thalassemia and sickle cell disease: past, present and future.
Ischaemia-induced muscle metabolic abnormalities are poorly alleviated by endurance training in a mouse model of sickle cell disease.
Moderate and intense muscular exercises induce marked intramyocellular metabolic acidosis in sickle cell disease mice.
Acidosis, Respiratory
Chlorine inhalation induces acute chest syndrome in humanized sickle cell mouse model and ameliorated by postexposure hemopexin.
Acne Vulgaris
A Phase 1 Randomized, Placebo-Controlled Trial With a Topical Inhibitor of Stearoyl-Coenzyme A Desaturase 1 Under Occluded and Nonoccluded Conditions.
From pathogenesis of acne vulgaris to anti-acne agents.
Sequence analysis and characterization of FAR-17c, an androgen-dependent gene in the flank organs of hamsters.
Acquired Immunodeficiency Syndrome
Cardiac Magnetic Resonance in Primary Prevention of Sudden Cardiac Death.
Effect of Left Ventricular Dysfunction and Viral Load on Risk of Sudden Cardiac Death in Patients With Human Immunodeficiency Virus.
From Elephants to AIDS. Essays in biology in honor of Roger V. Short: Papers from the Havenmeyer Foundation Symposium to celebrate the life and work of Professor Roger V. Short ScD, FRS. June 27-30, 2001. Port Douglas, Australia.
Implantable defibrillators: from the adult cardiac to the grown up congenital heart disease patient.
Long-term central venous access in patients with sickle cell disease. Incidence of thrombotic and infectious complications.
The interaction between sickle cell disease and HIV infection: a systematic review.
The presentation, management and prevention of crisis in sickle cell disease in Africa.
Transfusion-transmitted malaria masquerading as sickle cell crisis with multisystem organ failure.
Acromegaly
Immunohistochemical analysis of 11-beta-hydroxysteroid dehydrogenase type 2 and glucocorticoid receptor in subclinical Cushing's disease due to pituitary macroadenoma.
Multihormonal pituitary adenoma concomitant with Pit-1 and Tpit lineage cells causing acromegaly associated with subclinical Cushing's disease: a case report.
Acute Chest Syndrome
A nontransfusional perioperative management regimen for patients with sickle cell disease undergoing laparoscopic cholecystectomy.
Acute chest syndrome in adult Afro-Caribbean patients with sickle cell disease. Analysis of 81 episodes among 53 patients.
Acute chest syndrome in the postoperative sickle cell patient.
Acute kidney injury in sickle patients with painful crisis or acute chest syndrome and its relation to pulmonary hypertension.
Airway hyperreactivity is frequent in non-asthmatic children with sickle cell disease.
Airway inflammation in sickle cell disease-A translational perspective.
An evidence-based approach to the treatment of adults with sickle cell disease.
Association between clinical outcomes and metformin use in adults with sickle cell disease and diabetes mellitus.
Association between plasma free haem and incidence of vaso-occlusive episodes and acute chest syndrome in children with sickle cell disease.
Association of Antibiotic Choice With Hospital Length of Stay and Risk Factors for Readmission in Patients With Sickle Cell Disease and Acute Chest Syndrome: An Observational Cohort Study.
Association of Guideline-Adherent Antibiotic Treatment With Readmission of Children With Sickle Cell Disease Hospitalized With Acute Chest Syndrome.
Association of hospital and provider types on sickle cell disease outcomes.
Asthma in children with sickle cell disease and its association with acute chest syndrome.
Asthma management in sickle cell disease.
Asthma management: reinventing the wheel in sickle cell disease.
Beneficial effect of intravenous dexamethasone in children with mild to moderately severe acute chest syndrome complicating sickle cell disease.
Blood transfusions for treating acute chest syndrome in people with sickle cell disease.
Care of the child with sickle cell disease: acute complications.
Cerebral fat embolism syndrome in sickle cell disease without evidence of shunt.
Chlamydia pneumoniae and acute chest syndrome in patients with sickle cell disease.
Circulating platelet and erythrocyte microparticles in young children and adolescents with sickle cell disease: Relation to cardiovascular complications.
Clinical correlates of steady-state oxyhaemoglobin desaturation in children who have sickle cell disease.
Clinical factors and incidence of acute chest syndrome or pneumonia among children with sickle cell disease presenting with a fever: a 17-year review.
Common Complications of Sickle Cell Disease: A Simulation-Based Curriculum.
Comorbid obstructive sleep apnea and increased risk for sickle cell disease morbidity.
Comparison of pneumococcal vaccination response in children with sickle cell disease: HbSS and HbSC.
Cost-effectiveness of adenotonsillectomy in reducing obstructive sleep apnea, cerebrovascular ischemia, vaso-occlusive pain, and ACS episodes in pediatric sickle cell disease.
Current issues in blood transfusion for sickle cell disease.
Decreased exhaled nitric oxide in sickle cell disease: relationship with chronic lung involvement.
Differential gene expression in pulmonary artery endothelial cells exposed to sickle cell plasma.
Echocardiographic abnormalities in sickle cell disease.
Eicosanoids in sickle cell disease: potential relevance of neutrophil leukotriene B4 to disease pathophysiology.
Elevation of tricuspid regurgitant jet velocity, a marker for pulmonary hypertension in children with sickle cell disease.
Emergency Medicine Management of Sickle Cell Disease Complications: An Evidence-Based Update.
Evidence review of hydroxyurea for the prevention of sickle cell complications in low-income countries.
Evidence-based management of sickle cell disease in the emergency department.
Extracorporeal membrane oxygenation for the treatment of adult sickle cell acute chest syndrome.
Gene-centric association study of acute chest syndrome and painful crisis in sickle cell disease patients.
Genetic modifiers of severity in sickle cell disease.
Glomerular lesions in patients with sickle cell disease.
Haemoglobin F modulation in childhood sickle cell disease.
Hemoglobinopathy and pediatrics in the time of COVID-19.
Hyperhemolysis Syndrome in a Patient with Sickle Cell Disease: A Case Report.
Identifying Clinical and Research Priorities in Sickle Cell Lung Disease. An Official American Thoracic Society Workshop Report.
Impact of acute chest syndrome on lung function of children with sickle cell disease.
Inflammation in sickle cell disease.
Influence of beta-cluster haplotypes, alpha-gene status and UGTA1 polymorphism on clinical and hematological data in sickle-cell disease children from French Guiana.
Integrating Fat Embolism Syndrome Scoring Indices in Sickle Cell Disease: A Practice Management Review.
Laparoscopic splenic procedures in children: experience in 231 children.
Leukotriene pathway in sickle cell disease: a potential target for directed therapy.
Life threatening parvovirus B19 and herpes simplex virus associated acute myocardial dysfunction in a child with homozygous sickle cell disease.
Lipid profiles in French West Indies sickle cell disease cohorts, and their general population.
Low-risk factors for severe bacterial infection and acute chest syndrome in children with sickle cell disease.
Lower airway obstruction is associated with increased morbidity in children with sickle cell disease.
Lung vaso-occlusion in sickle cell disease mediated by arteriolar neutrophil-platelet microemboli.
Management of sickle cell disease: summary of the 2014 evidence-based report by expert panel members.
Methacholine challenge in children with sickle cell disease: a case series.
Microfluidics in Sickle Cell Disease Research: State of the Art and a Perspective Beyond the Flow Problem.
Mortality in sickle cell disease: A population-based study in an aboriginal community in the Gudalur Valley, Nilgiris, Tamil Nadu, India.
Mortality, asthma, smoking and acute chest syndrome in young adults with sickle cell disease.
Multi-modal intervention for the inpatient management of sickle cell pain significantly decreases the rate of acute chest syndrome.
Multiple sclerosis in a young woman with sickle cell disease.
Neurologic and Cognitive Outcomes in Sickle Cell Disease from Infancy through Adolescence.
New approaches to hematopoietic cell transplantation for hematological diseases in children.
Nocturnal hypoxemia measured by polysomnogram is associated with acute chest syndrome in pediatric sickle cell disease.
Osteonecrosis of the femoral head in sickle cell disease: prevalence, comorbidities, and surgical outcomes in California.
Outcome of Pregnancy in Saudi Women with Sickle Cell Disease Attending the Tertiary Care University Hospital in Eastern Province of Saudi Arabia.
Perioperative Management of Sickle Cell Disease.
Physician-diagnosed asthma and acute chest syndrome: associations with NOS polymorphisms.
Placenta growth factor in sickle cell disease: association with hemolysis and inflammation.
Polymorphisms in Inflammatory Genes Modulate Clinical Complications in Patients With Sickle Cell Disease.
Predictors of mortality in adults with Sickle cell disease admitted to intensive care unit in Bahrain.
Prevalence and factors associated with renal dysfunction among children with sickle cell disease attending the sickle cell disease clinic at a tertiary hospital in Northwestern Tanzania.
Prevalence of pulmonary hypertension in sickle cell anaemia patients of a tertiary hospital in Nigeria.
Prophylactic laparoscopic cholecystectomy in adult sickle cell disease patients with cholelithiasis: A prospective cohort study.
Pulmonary complications of hemoglobinopathies.
Pulmonary complications of sickle cell disease.
Pulmonary disease burden in Hispanic and non-Hispanic children with sickle cell disease.
Pulmonary Function Abnormalities and Asthma Are Prevalent in Children with Sickle Cell Disease and Are Associated with Acute Chest Syndrome.
Pulmonary Function and Airway Hyperresponsiveness in Adults with Sickle Cell Disease.
Pulmonary function studies in Kuwaiti children with sickle cell disease and elevated Hb F.
Pulmonary functions in children and adolescents with sickle cell disease.
Pulmonary hypertension in children and adolescents with sickle cell disease.
Quantitative intravital two-photon excitation microscopy reveals absence of pulmonary vaso-occlusion in unchallenged Sickle Cell Disease mice.
Red blood cell alloimmunization in sickle cell disease: prevalence in 2010.
Red blood cell transfusion to treat or prevent complications in sickle cell disease: an overview of Cochrane reviews.
Redox-dependent impairment of vascular function in sickle cell disease.
Relation between glutathione S-transferase genes (GSTM1, GSTT1, and GSTP1) polymorphisms and clinical manifestations of sickle cell disease in Egyptian patients.
Role of hydroxycarbamide in prevention of complications in patients with sickle cell disease.
Secondhand Smoke Is an Important Modifiable Risk Factor in Sickle Cell Disease: A Review of the Current Literature and Areas for Future Research.
Selective prophylactic transfusion in sickle cell disease.
Sickle cell anemia in the pediatric intensive care unit: novel approaches for managing life-threatening complications.
Sickle cell disease and venous thromboembolism: what the anticoagulation expert needs to know.
Sickle cell disease as a vascular disorder.
Sickle cell disease in children.
Sickle cell disease patients in eastern province of Saudi Arabia suffer less severe acute chest syndrome than patients with African haplotypes.
Sickle cell disease subphenotypes in patients from southwestern province of saudi arabia.
Sickle cell disease: management options and challenges in developing countries.
Sickle cell disease: the need for a public health agenda.
Sickle cell disease: when and how to transfuse.
Sickle cell leg ulcers: a frequently disabling complication and a marker of severity.
Sickle erythrocytes and platelets augment lung leukotriene synthesis with downregulation of anti-inflammatory proteins: relevance in the pathology of the acute chest syndrome.
Soluble CD163 in young sickle cell disease patients and their trait siblings: a biomarker for pulmonary hypertension and vaso-occlusive complications.
Soluble MD-2 and Heme in Sickle Cell Disease Plasma Promote Pro-Inflammatory Signaling in Endothelial Cells.
Spontaneous breathing during extracorporeal membrane oxygenation treatment of sickle cell disease acute chest syndrome.
Stable to improved cardiac and pulmonary function in children with high-risk sickle cell disease following haploidentical stem cell transplantation.
Steady-state sVCAM-1 serum levels in adults with sickle cell disease.
Streptococcus pneumoniae and Its Virulence Factors H2O2 and Pneumolysin Are Potent Mediators of the Acute Chest Syndrome in Sickle Cell Disease.
Tandem P-selectin glycoprotein ligand immunoglobulin prevents lung vaso-occlusion in sickle cell disease mice.
The Acute Chest Syndrome in Cameroonian children living with sickle cell disease.
The acute chest syndrome of sickle cell disease following aortic valve replacement.
The burden of respiratory syncytial virus infections among children with sickle cell disease.
The clinical severity of hemoglobin S/Black ((A) ???)(0) -thalassemia.
The Impact of Recurrent Acute Chest Syndrome on the Lung Function of Young Adults with Sickle Cell Disease.
The Role of Inflammation and Leukocytes in the Pathogenesis of Sickle Cell Disease.
The Role of Inflammation and Leukocytes in the Pathogenesis of Sickle Cell Disease; Haemoglobinopathy.
Thromboinflammatory mechanisms in sickle cell disease - challenging the hemostatic balance.
Total Hip Arthroplasty in Patients With Sickle Cell Disease: A Comprehensive Systematic Review.
Transfusion therapy for sickle cell disease: a balancing act.
Utility of Point-of-Care Lung Ultrasonography for Evaluating Acute Chest Syndrome in Young Patients With Sickle Cell Disease.
Vascular Permeability Drives Susceptibility to Influenza Infection in a Murine Model of Sickle Cell Disease.
Vaso-occlusive crisis-associated neutrophil dysfunction in patients with sickle-cell disease.
Venous thromboembolism in pregnant women with sickle cell disease: a retrospective database analysis.
Vitamin D deficiency and acute vaso-occlusive complications in children with sickle cell disease.
Which Febrile Children with Sickle Cell Disease Need a Chest X-Ray?
[Infectious complications after surgical splenectomy in children with sickle cell anemia disease].
[Successful management of acute chest syndrome in a patient with sickle cell disease].
Acute Coronary Syndrome
A case-control study between gene polymorphisms of polyunsaturated fatty acid metabolic rate-limiting enzymes and acute coronary syndrome in Chinese Han population.
Cardiac arrhythmias and conduction disturbances in autoimmune rheumatic diseases.
Morphologic features of culprit lesions in sudden coronary death with family history of premature coronary artery disease.
Myocardial ischemia and ventricular tachycardia on continuous electrocardiographic monitoring and risk of cardiovascular outcomes after non-ST-segment elevation acute coronary syndrome (from the MERLIN-TIMI 36 Trial).
Relationship between nonsustained ventricular tachycardia after non-ST-elevation acute coronary syndrome and sudden cardiac death: observations from the metabolic efficiency with ranolazine for less ischemia in non-ST-elevation acute coronary syndrome-thrombolysis in myocardial infarction 36 (MERLIN-TIMI 36) randomized controlled trial.
Right single coronary artery as an incidental finding in Takotsubo syndrome and acute heart failure: Case report and review of the literature.
Sudden death among the Israeli civilian population during the Gulf War--incidence and mechanisms.
Acute Kidney Injury
Acute hydroxyurea treatment reduces tubular damage following bilateral ischemia-reperfusion injury in a mouse model of sickle cell disease.
Acute kidney injury in sickle patients with painful crisis or acute chest syndrome and its relation to pulmonary hypertension.
Early and prominent alterations in hemodynamics, signaling, and gene expression following renal ischemia in sickle cell disease.
Molecular Fingerprints of Borderline Changes in Kidney Allografts Are Influenced by Donor Category.
Outcomes and utilization of kidneys from deceased donors with acute kidney injury.
Perioperative Management of Sickle Cell Disease.
Sickle cell disease in pregnancy: maternal complications in a medicaid-enrolled population.
Sickle cell disease is associated with higher mortality among patients hospitalized with ischemic bowel disease.
Acute Lung Injury
Chlorine inhalation induces acute chest syndrome in humanized sickle cell mouse model and ameliorated by postexposure hemopexin.
Protective effects of S-nitrosoalbumin on lung injury induced by hypoxia-reoxygenation in mouse model of sickle cell disease.
Tandem P-selectin glycoprotein ligand immunoglobulin prevents lung vaso-occlusion in sickle cell disease mice.
adamts13 endopeptidase deficiency
ADAMTS13 activity in sickle cell disease.
Dynamics of von Willebrand factor reactivity in sickle cell disease during vaso-occlusive crisis and steady state.
Haemoglobin blocks von Willebrand factor proteolysis by ADAMTS-13: a mechanism associated with sickle cell disease.
Adenocarcinoma
Endogenous n-3 polyunsaturated fatty acids delay progression of pancreatic ductal adenocarcinoma in Fat-1-p48(Cre/+)-LSL-Kras(G12D/+) mice.
Inhibition of Stearoyl-CoA Desaturase Induces the Unfolded Protein Response in Pancreatic Tumors and Suppresses Their Growth.
Loss of stearoyl-CoA desaturase expression is a frequent event in prostate carcinoma.
Stearoyl-CoA desaturase activity in mammary adenocarcinomas carried by C3H mice.
[Impact of androgen deprivation prior to radical prostatectomy for T1, T2 prostate cancer on the likelihood of curative surgery]
Adenocarcinoma of Lung
Inhibition of Stearoyl-CoA Desaturase 1 expression in human lung adenocarcinoma cells impairs tumorigenesis.
Adenoma
Altered Saturated and Monounsaturated Plasma Phospholipid Fatty Acid Profiles in Adult Males with Colon Adenomas.
Is there an added value of faecal calprotectin and haemoglobin in the diagnostic work-up for primary care patients suspected of significant colorectal disease? A cross-sectional diagnostic study.
Adrenal Insufficiency
Lower hair cortisol among patients with sickle cell disease may indicate decreased adrenal reserves.
Airway Obstruction
Airway Inflammation and Lung Function in Sickle Cell Disease.
Lower airway obstruction is associated with increased morbidity in children with sickle cell disease.
Sickle cell disease: wheeze or asthma?
Albinism, Oculocutaneous
Severity in phenotypic expression of homozygous sickle cell disease (Hb.SS) - Does hypermelanotic or hypomelanotic skin status of affected patients play a role?
Albuminuria
Albuminuria Is Associated with Endothelial Dysfunction and Elevated Plasma Endothelin-1 in Sickle Cell Anemia.
Albuminuria, kidney function, and sudden cardiac death: Findings from The Reasons for Geographic and Racial Differences in Stroke (REGARDS) study.
Cardiorenal Risk Prevalence in Sickle Cell Hemoglobinopathy.
Changes in Conjunctival Hemodynamics Predict Albuminuria in Sickle Cell Nephropathy.
Changes in urine albumin to creatinine ratio with the initiation of hydroxyurea therapy among children and adolescents with sickle cell disease.
Engulfment and cell motility 1 (ELMO1) and apolipoprotein A1 (APOA1) as candidate genes for sickle cell nephropathy.
Higher rates of hemolysis are not associated with albuminuria in Jamaicans with sickle cell disease.
Intravenous infusion of haptoglobin for the prevention of adverse clinical outcome in Sickle Cell Disease.
Kidney Disease among Patients with Sickle Cell Disease, Hemoglobin SS and SC.
Novel marker for the detection of sickle cell nephropathy: soluble FMS-like tyrosine kinase-1 (sFLT-1).
Prevalence and factors associated with renal dysfunction among children with sickle cell disease attending the sickle cell disease clinic at a tertiary hospital in Northwestern Tanzania.
Risk factors for conjunctival and retinal vessel alterations in sickle cell disease.
Roles of APOL1 G1 and G2 variants in sickle cell disease patients: kidney is the main target.
Serum cystatin C levels in children with sickle cell disease.
Short-term follow-up of patients with sickle cell disease and albuminuria.
Sickle cell disease and albuminuria: recent advances in our understanding of sickle cell nephropathy.
Sickle cell disease nephropathy: an update on risk factors and potential biomarkers in pediatric patients.
Soluble Fas/FasL ratio as a marker of vasculopathy in children and adolescents with sickle cell disease.
The glomerulopathy of sickle cell disease.
Urinary albumin excretion is associated with pulmonary hypertension in sickle cell disease: potential role of soluble fms-like tyrosine kinase-1.
Alopecia
Cystathionine ?-synthase-deficient mice thrive on a low-methionine diet.
The earlobe crease, coronary artery disease, and sudden cardiac death: an autopsy study of 520 individuals.
alpha-Thalassemia
Genetic modifiers of severity in sickle cell disease.
Mutations and polymorphisms in hemoglobin genes and the risk of pulmonary hypertension and death in sickle cell disease.
Varied Age of First Presentation of Sickle Cell Disease: Case Presentations and Review.
[Neonatal screening of hemoglobinopathies and G6PD deficiency in Catalonia (Spain). Molecular study of sickle cell disease associated with alpha thalassemia and G6PD deficiency]
Alzheimer Disease
A Conceptualization of the Utility of Subjective Cognitive Decline in Clinical Trials of Preclinical Alzheimer's Disease.
Activities of Daily Living and Depressive Symptoms in Patients with Subjective Cognitive Decline, Mild Cognitive Impairment, and Alzheimer's Disease.
Alterations in Dynamic Functional Connectivity in Individuals With Subjective Cognitive Decline.
An approach to classifying subjective cognitive decline in community-dwelling elders.
Attention capacity and self-report of subjective cognitive decline: a P3 ERP study.
Auditory Verbal Learning Test is Superior to Rey-Osterrieth Complex Figure Memory for Predicting Mild Cognitive Impairment to Alzheimer's Disease.
Blood NCAPH2 Methylation Is Associated With Hippocampal Volume in Subjective Cognitive Decline With Apolipoprotein E ?4 Non-carriers.
Brain connectivity and metacognition in persons with subjective cognitive decline (COSCODE): rationale and study design.
Changes in Centrality Frequency of the Default Mode Network in Individuals With Subjective Cognitive Decline.
Clinical Characteristics in Subjective Cognitive Decline with and without Worry: Baseline Investigation of the SILCODE Study.
Cognitive performance before and after the onset of subjective cognitive decline in old age.
Development of a subjective cognitive decline questionnaire using item response theory: a pilot study.
Differential neural structures, intrinsic functional connectivity, and episodic memory in subjective cognitive decline and healthy controls.
Differential Risk of Incident Alzheimer's Disease Dementia in Stable Versus Unstable Patterns of Subjective Cognitive Decline.
Distinct Profile Differences in Subjective Cognitive Decline in the General Public Are Associated with Metacognition, Negative Affective Symptoms, Neuroticism, Stress, and Poor Quality of Life.
Dynamics and Concordance Abnormalities Among Indices of Intrinsic Brain Activity in Individuals With Subjective Cognitive Decline: A Temporal Dynamics Resting-State Functional Magnetic Resonance Imaging Analysis.
Effects of spermidine supplementation on cognition and biomarkers in older adults with subjective cognitive decline (SmartAge)-study protocol for a randomized controlled trial.
Efficacies of Cognitive Interventions in the Elderly with Subjective Cognitive Decline: A Prospective, Three-Arm, Controlled Trial.
Efficacy and neural mechanism of acupuncture treatment in older adults with subjective cognitive decline: study protocol for a randomised controlled clinical trial.
Elevated stearoyl-CoA desaturase in brains of patients with Alzheimer's disease.
Enhancing 'meaningfulness' of functional assessments: UK adaptation of the Amsterdam IADL questionnaire.
Enhancing Working Memory Based on Mismatch Negativity Neurofeedback in Subjective Cognitive Decline Patients: A Preliminary Study.
Evolving Evidence for the Value of Neuroimaging Methods and Biological Markers in Subjects Categorized with Subjective Cognitive Decline.
Exploring APOE genotype effects on Alzheimer's disease risk and amyloid ? burden in individuals with subjective cognitive decline: The FundacioACE Healthy Brain Initiative (FACEHBI) study baseline results.
From Subjective Cognitive Decline to Alzheimer's Disease: The Predictive Role of Neuropsychological Assessment, Personality Traits, and Cognitive Reserve. A 7-Year Follow-Up Study.
Identification of Earlier Biomarkers for Alzheimer's Disease: A Multimodal Neuroimaging Study of Individuals with Subjective Cognitive Decline.
Impaired Memory Awareness and Loss Integration in Self-Referential Network Across the Progression of Alzheimer's Disease Spectrum.
Influence of Sampling and Recruitment Methods in Studies of Subjective Cognitive Decline.
KIBRA T allele influences memory performance and progression of cognitive decline: a 7-year follow-up study in subjective cognitive decline and mild cognitive impairment.
Mediterranean Diet, Alzheimer Disease Biomarkers and Brain Atrophy in Old Age.
Memory difficulties are not always a sign of incipient dementia: a review of the possible causes of loss of memory efficiency.
Personality Factors and Subjective Cognitive Decline: The FACEHBI Cohort.
Prevention of cognitive decline in subjective cognitive decline APOE ?4 carriers after EGCG and a multimodal intervention (PENSA): Study design.
Qualitative and quantitative assessment of self-reported cognitive difficulties in nondemented elders: Association with medical help seeking, cognitive deficits, and ?-amyloid imaging.
Recurrent and concurrent patterns of regional BOLD dynamics and functional connectivity dynamics in cognitive decline.
Region-Specific Association of Subjective Cognitive Decline With Tauopathy Independent of Global ?-Amyloid Burden.
Resting State BOLD Variability Is Linked to White Matter Vascular Burden in Healthy Aging but Not in Older Adults With Subjective Cognitive Decline.
Risk Factors and Neuropsychological Assessments of Subjective Cognitive Decline (plus) in Chinese Memory Clinic.
Risk factors for amyloid positivity in older people reporting significant memory concern.
Subjective cognitive complaints at age 70: associations with amyloid and mental health.
Subjective Cognitive Decline and Alzheimer's Disease Spectrum Disorder.
Subjective cognitive decline in cognitively normal elders from the community or from a memory clinic: Differential affective and imaging correlates.
Subjective Cognitive Decline May Be a Stronger Predictor of Incident Dementia in Women than in Men.
Subjective cognitive decline, brain imaging biomarkers, and cognitive functioning in patients with a history of vascular disease: the SMART-Medea study.
The characterisation of subjective cognitive decline.
The interplay between gray matter and white matter neurodegeneration in subjective cognitive decline.
The Subjective Cognitive Decline Questionnaire (SCD-Q): A Validation Study.
Using Neuropsychological Process Scores to Identify Subtle Cognitive Decline and Predict Progression to Mild Cognitive Impairment.
White matter and its relationship with cognition in subjective cognitive decline.
[Research Advances in Interventions on Subjective Cognitive Decline].
[Study on argyrophilic inclusions of multisystem atrophy (Oppenheimer)]
Amyloidosis
Correlations between plasma and PET beta-amyloid levels in individuals with subjective cognitive decline: the Fundació ACE Healthy Brain Initiative (FACEHBI).
Prophylactic implantation of cardioverter-defibrillator in patients with severe cardiac amyloidosis and high risk for sudden cardiac death.
Sickle cell disease: a case report of renal amyloidosis.
The relationship between white matter microstructure and self-perceived cognitive decline.
[Antiarrhythmic agents in the prevention of sudden cardiac death]
Amyotrophic Lateral Sclerosis
Sudden cardiac death in neuromuscular disorders.
The Level of Serum Pepsinogen in Diagnosing and Evaluating the Severity of Subacute Combined Degeneration Due to Vitamin B12 Deficiency.
Anaphylaxis
Contact dermatitis as a systemic disease.
Anemia
-
A case report of darbepoetin treatment in a patient with sickle cell disease and chronic renal failure undergoing regular hemodialysis procedures that induce a dose-dependent extension of blood transfusion intervals.
A history of repetitive cesarean section is a risk factor of anemia in healthy perimenopausal women: The Korea National Health and Nutrition Examination Survey 2010-2012.
A Qualitative Study of Chronic Pain and Self-Management in Adults with Sickle Cell Disease.
A retrospective study of 23 cases with subacute combined degeneration.
A ten year review of the sickle cell program in Muhimbili National Hospital, Tanzania.
Abnormal Regulation of Microvascular Tone in a Murine Model of Sickle Cell Disease Assessed by Contrast Ultrasound.
Acute leukemia in sickle cell disease patients in a tertiary health facility in Nigeria: a case series.
Acute silent cerebral ischemia and infarction during acute anemia in children with and without sickle cell disease.
Acute soft head syndrome in children with sickle cell anaemia in lagos, Nigeria.
Adolescents with sickle cell disease in a rural community: are they ready to transition to adulthood?
Allogenic hematopoietic stem cell transplantation in sickle cell disease.
Amelioration of murine sickle cell disease by nonablative conditioning and ?-globin gene-corrected bone marrow cells.
An observational study of children with sickle cell disease in Kilifi, Kenya.
Analysis of Causes of Hospitalization Among Children with Sickle Cell Disease in a Group of Private Hospitals in Jeddah, Saudi Arabia.
Angiopoietin-2 as a Marker of Retinopathy in Children and Adolescents With Sickle Cell Disease: Relation to Subclinical Atherosclerosis.
Assessment of Hemoglobin Variants in Patients Receiving Health Care at the Ho Teaching Hospital: A Three-Year Retrospective Study.
Association between apolipoprotein epsilon4 allele, factor V Leiden, and plasma lipid and lipoprotein levels with sickle cell disease in southern Iran.
Association of Anemia and Blood Pressure With Novel Markers of Diastolic Function in Pediatric Sickle Cell Disease.
Associations between TGF-?1 Levels and Markers of Hemolysis, Inflammation, and Tissue Remodeling in Pediatric Sickle Cell Patients.
Beta-thalassaemia and sickle cell anaemia as paradigms of hypercoagulability.
Brain Perfusion Impairment in Neurologically Asymptomatic Adult Patients with Sickle-Cell Disease Shown by Voxel-Based Analysis of SPECT Images.
Cardiorenal Risk Prevalence in Sickle Cell Hemoglobinopathy.
Cardiovascular manifestations of sickle cell disease.
Care of the child with sickle cell disease: acute complications.
Causes of hospitalization in sickle cell diseased children in western region of Saudi Arabia. A single center study.
Cell and Gene Therapy for Anemia: Hematopoietic Stem Cells and Gene Editing.
Clinical correlates of steady-state oxyhaemoglobin desaturation in children who have sickle cell disease.
Cognitive and behavior deficits in sickle cell mice are associated with profound neuropathologic changes in hippocampus and cerebellum.
Cognitive behavioral therapy in patients with sickle cell disease.
Comorbidity of Glucose-6-Phosphate Dehydrogenase Deficiency and Sickle Cell Disease Exert Significant Effect on RBC Indices.
Consequences and management of iron overload in sickle cell disease.
Contrasting resting-state fMRI abnormalities from sickle and non-sickle anemia.
Contribution of spinal MRI for unsuspected cobalamin deficiency in isolated sub-acute combined degeneration.
Correlation between anemia and clinical severity in subacute combined degeneration patients.
Decreased Hepcidin Levels Are Associated with Low Steady-state Hemoglobin in Children With Sickle Cell Disease in Tanzania.
Defective regulation of complement by the sickle erythrocyte: evidence for a defect in control of membrane attack complex formation.
Degree of Anemia, Indirect Markers of Hemolysis, and Vascular Complications of Sickle Cell Disease in Africa.
Delayed Hemolytic Transfusion Reaction in a Sickle Cell Disease Patient: A Case Report.
Delayed hemolytic transfusion reaction/hyperhemolysis syndrome in children with sickle cell disease.
Diagnosing sickle cell disease and iron deficiency anemia in human blood by Raman spectroscopy.
Dietary nonheme iron is equally bioavailable from ferritin or ferrous sulfate in thalassemia intermedia.
Dynamic vascular analysis shows a hyperemic flow pattern in sickle cell disease.
Effect of transfusion therapy on transcranial doppler ultrasonography velocities in children with sickle cell disease.
Epidemiology and treatment of relative anemia in children with sickle cell disease in sub-Saharan Africa.
Evaluation of point-of-care International Normalized Ratio in sickle cell disease.
Exercise tolerance, lung function abnormalities, anemia, and cardiothoracic ratio in sickle cell patients.
Expression pattern of CD55 and CD59 on red blood cells in sickle cell disease.
Extracellular Vesicles in Sickle Cell Disease: Plasma Concentration, Blood Cell Types Origin Distribution and Biological Properties.
Extramedullary hematopoiesis of the liver in a child with sickle cell disease: A rare complication.
Factor V Leiden G1691A and prothrombin G20210A mutations among Palestinian patients with sickle cell disease.
Foetal haemoglobin, erythrocytes containing foetal haemoglobin, and hematological features in congolese patients with sickle cell anaemia.
Folate supplementation in people with sickle cell disease.
Functional capacity in children and young adults with sickle cell disease undergoing evaluation for cardiopulmonary disease.
GBT440 Increases Hematocrit and Improves Biventricular Function in Berkeley Sickle Cell Disease Mice.
Genome-wide association study of erythrocyte density in sickle cell disease patients.
Glomerular function in sickle cell disease patients during crisis.
Glutathione S-transferase gene polymorphisms (GSTM1, GSTT1, and GSTP1) in Egyptian pediatric patients with sickle cell disease.
Growth differentiation factor-15 in young sickle cell disease patients: relation to hemolysis, iron overload and vascular complications.
Heamostatic and genetic predisposing factors for stroke in children with sickle cell anemia.
Helicobacter pylori infection in sickle cell disease.
Hematological profile of sickle cell disease from South Gujarat, India.
Hemin controls T cell polarization in sickle cell alloimmunization.
Hemoglobin level and macular thinning in sickle cell disease.
High levels of placenta growth factor in sickle cell disease promote pulmonary hypertension.
How I treat the older adult with sickle cell disease.
Hydroxyurea for the treatment of sickle cell disease.
Hydroxyurea Use Associated with Nonverbal and Executive Skills in Sickle Cell Anemia.
Hypoxia and inflammation in children with sickle cell disease: implications for hippocampal functioning and episodic memory.
Identification of genetic polymorphisms associated with risk for pulmonary hypertension in sickle cell disease.
Improved survival of children and adolescents with sickle cell disease.
Increased Red Blood Cell Stiffness Increases Pulmonary Vascular Resistance and Pulmonary Arterial Pressure.
Ineffective erythropoiesis in sickle cell disease: new insights and future implications.
Influence of sickle cell disease on susceptibility to HIV infection.
Interactions of biomedical and environmental risk factors for cognitive development: a preliminary study of sickle cell disease.
Interleukin-1 receptor inhibition reduces stroke size in a murine model of sickle cell disease.
Intestine-specific Disruption of Hypoxia-inducible Factor (HIF)-2? Improves Anemia in Sickle Cell Disease.
Iron deficiency anaemia in Jamaican children, aged 1-5 years, with sickle cell disease.
Iron stores in pregnant women with sickle cell disease: a protocol for a systematic review and meta-analysis.
Is sickle cell disease sufficiently prioritized in policy and socio-economic research on diseases in Tanzania? Lessons for the past 50 years.
Is Skeletal Muscle Dysfunction a Limiting Factor of Exercise Functional Capacity in Patients with Sickle Cell Disease?
Low hemoglobin increases risk for cerebrovascular disease, kidney disease, pulmonary vasculopathy, and mortality in sickle cell disease: A systematic literature review and meta-analysis.
Management of sickle cell disease: summary of the 2014 evidence-based report by expert panel members.
Management of the Dialysis Patient with Sickle Cell Disease.
Morbidity and pregnancy outcomes associated with sickle cell anemia among Saudi women.
Mortality in sickle cell disease: A population-based study in an aboriginal community in the Gudalur Valley, Nilgiris, Tamil Nadu, India.
mTOR Inhibition Improves Anaemia and Reduces Organ Damage in a Murine Model of Sickle Cell Disease.
Multisystem damage associated with tricorporal priapism in sickle cell disease.
Myocardial tissue characterization and the role of chronic anemia in sickle cell cardiomyopathy.
N-terminal pro-brain natriuretic peptide levels and risk of death in sickle cell disease.
Near-infrared spectra absorbance of blood from sickle cell patients and normal individuals.
Neurological PRESentations in Sickle Cell Patients Are Not Always Stroke: A Review of Posterior Reversible Encephalopathy Syndrome in Sickle Cell Disease.
New therapies in sickle cell disease.
Non-hematopoietic deficiency of proprotein convertase subtilisin/kexin type 9 deficiency leads to more severe anemia in a murine model of sickle cell disease.
Noninvasive optical assessment of resting-state cerebral blood flow in children with sickle cell disease.
Novel permeability characteristics of red blood cells from sickle cell patients heterozygous for HbS and HbC (HbSC genotype).
Outcome of pregnancies among women with sickle cell disease.
Outcome of Pregnancy in Saudi Women with Sickle Cell Disease Attending the Tertiary Care University Hospital in Eastern Province of Saudi Arabia.
Paediatric sickle cell disease: pulmonary hypertension but normal vascular resistance.
Pattern of Cerebral Blood Flow Velocity Using Transcranial Doppler Ultrasonography in Children with Sickle Cell Disorder in Lagos State, Nigeria.
Peripartum hyperhemolysis prophylaxis and management in sickle cell disease: A case report and narrative review.
Placenta growth factor augments endothelin-1 and endothelin-B receptor expression via hypoxia-inducible factor-1 alpha.
Placental histopathology in sickle cell disease: A descriptive and hypothesis-generating study.
Plasma Folate Levels in Acutely Ill and Steady State Pediatric Sickle Cell Disease Patients in Ghana.
Plasma Lipids and Lipoproteins in Sickle Cell Disease Patients in the Northern West Bank, Palestine.
Post-transfusion hyperhaemolysis in a patient with sickle cell disease: use of steroids and intravenous immunoglobulin to prevent further red cell destruction.
Potent and orally active purine-based fetal hemoglobin inducers for treating ?-thalassemia and sickle cell disease.
Preliminary Data on COVID-19 in Patients with Hemoglobinopathies: A Multicentre ICET-A Study.
Prevalence and factors associated with renal dysfunction among children with sickle cell disease attending the sickle cell disease clinic at a tertiary hospital in Northwestern Tanzania.
Prevalence of mitral valve prolapse in Saudi sickle cell disease patients in Dammam - A prospective-controlled echocardiographic study.
Pseudotumor cerebri in children with sickle cell disease: a case series.
Recommendations for the management of sickle cell disease in South Africa.
Relationship Between Anemia and Sudden Cardiac Death in Patients with Severe Aortic Stenosis.
Relationships between systemic vascular resistance, blood rheology and nitric oxide in children with sickle cell anemia or sickle cell-hemoglobin C disease.
Renal tubular dysfunction in children with sickle cell haemoglobinopathy.
Restless legs syndrome and sleep quality among adult sickle cell disease patients.
Semisynthetic supra plasma expanders: a new class of therapeutics to improve microcircualtion in sickle cell anaemia.
Sensorineural hearing loss in adults with sickle cell anaemia.
Serum Hepcidin Concentration in Individuals with Sickle Cell Anemia: Basis for the Dietary Recommendation of Iron.
Severe proliferative retinopathy is associated with blood hyperviscosity in sickle cell hemoglobin-C disease but not in sickle cell anemia.
Severity of Anaemia Has Corresponding Effects on Coagulation Parameters of Sickle Cell Disease Patients.
Sickle cell anemia and hematological neoplasias.
Sickle cell anemia in the pediatric intensive care unit: novel approaches for managing life-threatening complications.
Sickle cell disease and malaria: decreased exposure and asplenia can modulate the risk from Plasmodium falciparum.
Sickle cell disease in anaemic children in a Sierra Leonean district hospital: a case series.
Sickle cell disease subjects and mouse models have elevated nitrite and cGMP levels in blood compartments.
Sickle Cell Disease Subjects Have a Distinct Abnormal Autonomic Phenotype Characterized by Peripheral Vasoconstriction With Blunted Cardiac Response to Head-Up Tilt.
Sickle cell disease: Classification of clinical complications and approaches to preventive and therapeutic management.
Sickle cell disease: current clinical management.
Sickle cell disease: renal manifestations and mechanisms.
Simultaneous acute splenic sequestration and transient aplastic crisis in children with sickle cell disease.
Simultaneous point-of-care detection of anemia and sickle cell disease in Tanzania: the RAPID study.
Skeletal and myocardial microvascular blood flow in hydroxycarbamide-treated patients with sickle cell disease.
Sleep-disordered breathing and comorbidities: role of the upper airway and craniofacial skeleton.
Stroke in patients with sickle cell disease: clinical and neurological aspects.
Study of Adrenal Functions using ACTH stimulation test in Egyptian children with Sickle Cell Anemia: Correlation with Iron Overload.
Subacute combined degeneration without nutritional anemia.
Subacute combined degeneration: a case of pernicious anaemia without haematological manifestations.
Successful Treatment of Hepatitis C Virus by Ledipasvir/Sofosbuvir in a Cirrhotic Patient with Sickle Cell Disease and Thalassemia Minor.
Sudden cardiac death after acute decompensation in heart failure patients: implications of discharge haemoglobin levels.
Summer Camps for Children with Sickle Cell Disease.
Surfactant protein D as a marker for pulmonary complications in pediatric patients with sickle cell disease: Relation to lung function tests.
Sustained long-term hematologic efficacy of hydroxyurea at maximum tolerated dose in children with sickle cell disease.
Systematic review of current and emerging strategies for reducing morbidity from malaria in sickle cell disease.
Systematic Review of Voxelotor: A First-in-Class Sickle Hemoglobin Polymerization Inhibitor for Management of Sickle Cell Disease.
Techniques for the Detection of Sickle Cell Disease: A Review.
The clinical impact of MTHFR polymorphism on the vascular complications of sickle cell disease.
The clinical severity of hemoglobin S/Black ((A) ???)(0) -thalassemia.
The CYB5R3c.350C>G and G6PD A alleles modify severity of anemia in malaria and sickle cell disease.
The DAU Allele and Anti-D Alloimmunization Present With High Frequency in Brazilian Sickle Cell Disease Patients.
The Economic Burden of End-Organ Damage Among Medicaid Patients with Sickle Cell Disease in the United States: A Population-Based Longitudinal Claims Study.
The Effect of Hydroxyurea Therapy in Bahraini Sickle Cell Disease Patients.
The Effects of Treatment with Blood Transfusion, Iron Chelation and Hydroxyurea on Puberty, Growth and Spermatogenesis in Sickle Cell Disease (SCD): A short update.
The features of sickle cell disease in Saudi children.
The influence of infant and maternal sickle cell disease on birth outcome and neonatal course.
The metabolites of nitric oxide in sickle-cell disease.
The Need for Hematology Nurse Education in Low- and Middle-Income Countries: A Community Case Study in Tanzania.
The onset time of atracurium is prolonged in patients with sickle cell disease.
The radiological manifestations of sickle cell disease.
The severity of anaemia depletes cerebrovascular dilatory reserve in children with sickle cell disease: a quantitative magnetic resonance imaging study.
Thrombophilic mutations among Southern Iranian patients with sickle cell disease: high prevalence of factor V Leiden.
Tract-specific analysis and neurocognitive functioning in sickle cell patients without history of overt stroke.
Transcranial color Doppler in stroke-free adult patients with sickle cell disease.
Transcranial Doppler ultrasonography in adults with sickle cell disease.
Transfusion therapy for sickle cell disease: a balancing act.
Transient Hypoxia Model Revealed Cerebrovascular Impairment in Anemia Using BOLD MRI and Near-Infrared Spectroscopy.
Update of the Spanish registry of haemoglobinopathies in children and adults.
Urinary Transforming Growth Factor ?-1 as a Marker of Renal Dysfunction in Sickle Cell Disease.
Urinary transforming growth factor beta-1 as a marker of renal dysfunction in sickle cell disease.
Vitamin D level, lipid profile, and vitamin D receptor and transporter gene variants in sickle cell disease patients from Kurdistan of Iraq.
Voxelotor for the treatment of sickle cell disease.
Voxelotor: A Novel Treatment for Sickle Cell Disease.
When to transfuse blood in sickle cell disease? Lessons from Jehovah's Witnesses.
White blood cell count as a predictor of the severity of sickle cell disease during pregnancy.
[Association between subacute combined degeneration, vitamin B12 deficiency and megaloblastic anemia]
[Cytogenetic studies on 334 myelodysplastic syndrome (MDS), aplastic anemia (AA) and other hematological diseases]
[Transferrine soluble receptors' contribution to the assessment of iron status in homozygous drepanocytic anemia]
Anemia, Aplastic
Prevalence and Factors Associated with Human Parvovirus B19 Infection in Sickle Cell Patients Hospitalized in Tanzania.
Anemia, Diamond-Blackfan
Chronically Transfused Pediatric Sickle Cell Patients are Protected from Cardiac Iron Overload.
Anemia, Hemolytic
A phase 1/2 ascending dose study and open-label extension study of voxelotor in patients with sickle cell disease.
Big strokes in small persons.
Ceftriaxone-induced drug reaction mimicking acute splenic sequestration crisis in a child with hemoglobin SC disease.
Cerebrovascular reserve capacity is impaired in patients with sickle cell disease.
Detectable Unmetabolized Folic Acid and Elevated Folate Concentrations in Folic Acid-Supplemented Canadian Children With Sickle Cell Disease.
Effects of experimental asthma on inflammation and lung mechanics in sickle cell mice.
Factors Influencing Motivation and Engagement in Mobile Health Among Patients With Sickle Cell Disease in Low-Prevalence, High-Income Countries: Qualitative Exploration of Patient Requirements.
Femur Fracture in a Premature Infant: An Unusual Association of Sickle Cell Disease with Osteogenesis Imperfecta.
Fentanyl Buccal Tablet: A New Breakthrough Pain Medication in Early Management of Severe Vaso-Occlusive Crisis in Sickle Cell Disease.
Gastrointestinal pathology in sickle cell disease.
HCV Infection in Thalassemia Syndromes and Hemoglobinopathies: New Perspectives.
How we prevent and manage infection in sickle cell disease.
Imaging of musculoskeletal manifestations in sickle cell disease patients.
Lineage-specific BCL11A knockdown circumvents toxicities and reverses sickle phenotype.
Multiple complications in sickle cell anaemia.
New NO Donor NCX 1443: Therapeutic Effects on Pulmonary Hypertension in the SAD Mouse Model of Sickle Cell Disease.
Nrf2 activation in myeloid cells and endothelial cells differentially mitigates sickle cell disease pathology in mice.
Pathophysiology of Sickle Cell Disease.
Pharmacological inhibition of LSD1 and mTOR reduces mitochondrial retention and associated ROS levels in the red blood cells of sickle cell disease.
Psychiatric diagnosis in adolescents with sickle cell disease: a preliminary report.
Pulmonary complications of hemoglobinopathies.
Role of the coagulation system in the pathogenesis of sickle cell disease.
Sickle cell anemia and hematological neoplasias.
Sickle cell disease: a review for the internist.
Sickle cell disease: current treatment and emerging therapies.
Sickle cell diseases: What can nuclear medicine offer?
Splenectomy for haematological disorders: A single center study in 150 patients from Oman.
The association of transfusion status with antioxidant enzymes and malondialdehyde level in Nigerians with sickle cell disease.
The potential role of LSD1 inhibitors in the treatment of sickle cell disease: A review of preclinical animal model data.
Thyroid Function 'in Egyptian Children with Sickle Cell Anemia in correlation with iron' load.
Update: newborn screening for sickle cell disease--California, Illinois, and New York, 1998.
Anemia, Iron-Deficiency
Iron deficiency anaemia in Jamaican children, aged 1-5 years, with sickle cell disease.
Iron stores in pregnant women with sickle cell disease: a protocol for a systematic review and meta-analysis.
Anemia, Pernicious
Cobalamin (vitamin B(12)) in subacute combined degeneration and beyond: traditional interpretations and novel theories.
Pathogenesis of subacute combined degeneration: a result of methyl group deficiency.
Subacute combined degeneration: a case of pernicious anaemia without haematological manifestations.
Anemia, Refractory, with Excess of Blasts
[Cytogenetic studies on 334 myelodysplastic syndrome (MDS), aplastic anemia (AA) and other hematological diseases]
Anemia, Sickle Cell
"Body as a Machine": How Adolescents With Sickle Cell Disease Construct Their Fatigue Experiences.
A fluorescence method to detect and quantitate sterol esterification by lecithin:cholesterol acyltransferase.
A genetic variation associated with plasma erythropoietin and a non-coding transcript of PRKAR1A in Sickle Cell Disease.
A genetic variation associated with plasma erythropoietin and a non-coding transcript of PRKAR1A in sickle cell disease.
A high-fidelity Cas9 mutant delivered as a ribonucleoprotein complex enables efficient gene editing in human hematopoietic stem and progenitor cells.
A Needs Assessment of Persons With Sickle Cell Disease in a Major Medical Center in North Carolina.
A Qualitative Study of Chronic Pain and Self-Management in Adults with Sickle Cell Disease.
A Randomized Trial of Yoga for Children Hospitalized With Sickle Cell Vaso-Occlusive Crisis.
A simple, rapid, low-cost diagnostic test for sickle cell disease.
Acute Care Utilization at End of Life in Sickle Cell Disease: Highlighting the Need for a Palliative Approach.
Acute care utilization in pediatric sickle cell disease and sickle cell trait in the USA: prevalence, temporal trends, and cost.
Acute chest syndrome in the postoperative sickle cell patient.
Acute kidney injury in sickle patients with painful crisis or acute chest syndrome and its relation to pulmonary hypertension.
Acute soft head syndrome in children with sickle cell anaemia in lagos, Nigeria.
Adapting medical guidelines to be patient-centered using a patient-driven process for individuals with sickle cell disease and their caregivers.
Adolescents with sickle cell disease in a rural community: are they ready to transition to adulthood?
Adolescents with sickle cell disease: determinants of support group attendance and satisfaction.
Adverse Reactions to Pneumococcal Vaccine in Pediatric and Adolescent Patients with Sickle Cell Disease.
Alterations of lecithin cholesterol acyltransferase activity and apolipoprotein A-I functionality in human sickle blood.
Altered hematopoiesis in murine sickle cell disease.
Alternative complement pathway activity in sera from patients with sickle cell disease.
Alternative donor: ?ß/CD19 T-cell-depleted haploidentical hematopoietic stem cell transplantation for sickle cell disease.
An education program to increase teacher knowledge about sickle cell disease.
An Integrative Review of the Prevalence of Depression among Pediatric Patients with Sickle Cell Disease.
Angiopoietin-2 as a Marker of Retinopathy in Children and Adolescents With Sickle Cell Disease: Relation to Subclinical Atherosclerosis.
Ankylosis of the hips and knees due to sickle cell disease.
Anomalous renal effects of tin protoporphyrin in a murine model of sickle cell disease.
Antibiotic prophylaxis for children with sickle cell disease: a survey of pediatric dentistry residency program directors and pediatric hematologists.
Anxiety level and clinical course of patients with sickle cell disease during the COVID-19 outbreak.
Arginine therapy: a novel strategy to induce nitric oxide production in sickle cell disease.
Assessment of Hemoglobin Variants in Patients Receiving Health Care at the Ho Teaching Hospital: A Three-Year Retrospective Study.
Association between apolipoprotein epsilon4 allele, factor V Leiden, and plasma lipid and lipoprotein levels with sickle cell disease in southern Iran.
Association between elevated depressive symptoms and clinical disease severity in African-American adults with sickle cell disease.
Association between sickle cell disease and dental caries: a systematic review and meta-analysis.
Association of genetic variation in
Association of Guideline-Adherent Antibiotic Treatment With Readmission of Children With Sickle Cell Disease Hospitalized With Acute Chest Syndrome.
Associations between TGF-?1 Levels and Markers of Hemolysis, Inflammation, and Tissue Remodeling in Pediatric Sickle Cell Patients.
Attitudes of Primary Care Physicians Toward Sickle Cell Disease Care, Guidelines, and Comanaging Hydroxyurea With a Specialist.
Attitudes toward patients with sickle cell disease in a multicenter sample of emergency department providers.
Auditory-evoked response analysis in Brazilian patients with sickle cell disease.
Awareness of Ocular Manifestations, Complications, and Treatment of Sickle Cell Disease in the Eastern Province of Saudi Arabia: A Cross-Sectional Study.
Biocultural citizenship and embodying exceptionalism: Biopolitics for sickle cell disease in Brazil.
Bioelectrical impedance analysis of the body composition of children and adolescents with sickle cell disease.
Biomarkers and recent advances in the management and therapy of sickle cell disease.
Blood pressure in acute vaso-occlusive crises of sickle cell disease.
Blood transfusions for treating acute chest syndrome in people with sickle cell disease.
Bloodstream infection in adults with sickle cell disease: association with venous catheters, Staphylococcus aureus, and bone-joint infections.
Bone Marrow as a Hematopoietic Stem Cell Source for Gene Therapy in Sickle Cell Disease: Evidence from Rhesus and SCD Patients.
Brain neurochemical and hemodynamic findings in the NY1DD mouse model of mild sickle cell disease.
Brief report: Academic attainment in children with sickle cell disease.
Burden and spectrum of bacterial infections among sickle cell disease children living in Cameroon.
Cancer specific survival in patients with sickle cell disease.
CAREST-Multilingual Regional Integration for Health Promotion and Research on Sickle Cell Disease and Thalassemia.
Case Report: Psychosis in an adolescent with sickle cell disease.
CD209-336A/G promotor polymorphism and its clinical associations in sickle cell disease Egyptian Pediatric patients.
Cerebral blood flow measurement in children with sickle cell disease using continuous arterial spin labeling at 3.0-Tesla MRI.
Changes in Pain and Psychosocial Functioning and Transition to Chronic Pain in Pediatric Sickle Cell Disease: A Cohort Follow-up Study.
Changes in urine albumin to creatinine ratio with the initiation of hydroxyurea therapy among children and adolescents with sickle cell disease.
Characteristics of sickle cell patients with frequent emergency department visits and hospitalizations.
Choice of Donor Source and Conditioning Regimen for Hematopoietic Stem Cell Transplantation in Sickle Cell Disease.
Cholelithiasis in children with sickle cell disease.
Chronic blood exchange transfusions in the management of pre-capillary pulmonary hypertension complicating sickle cell disease.
Clinical and genetic ancestry profile of a large multi-centre sickle cell disease cohort in Brazil.
Clinical correlates of steady-state oxyhaemoglobin desaturation in children who have sickle cell disease.
Clinical events in a large prospective cohort of children with sickle cell disease in Nagpur, India: evidence against a milder clinical phenotype in India.
Clinical factors and incidence of acute chest syndrome or pneumonia among children with sickle cell disease presenting with a fever: a 17-year review.
Clinical findings associated with homozygous sickle cell disease in the Barbadian population--do we need a national SCD registry?
Clinical management of sickle cell liver disease in children and young adults.
Clinical relevance of pulmonary vasculature involvement in sickle cell disease.
Cobalamin status in sickle cell disease.
Coexistent Sickle Cell Disease Has No Impact on the Safety or Outcome of Lytic Therapy in Acute Ischemic Stroke: Findings From Get With The Guidelines-Stroke.
Cognitive Abilities Moderate the Effect of Disease Severity on Health-Related Quality of Life in Pediatric Sickle Cell Disease.
Cognitive functioning, patient health communication, and worry mediate pain predictive effects on health-related quality of life in youth with sickle cell disease.
Combined genetic disruption of K-Cl cotransporters and Gardos channel KCNN4 rescues erythrocyte dehydration in the SAD mouse model of sickle cell disease.
Combined liver-cytokine humanization comes to the rescue of circulating human red blood cells.
Common, But Neglected: A Comprehensive Review of Leg Ulcers in Sickle Cell Disease.
Community based screening for sickle haemoglobin among pregnant women in Benue State, Nigeria: I-Care-to-Know, a Healthy Beginning Initiative.
Comparative evaluation of oral and dento-maxillofacial manifestation of patients with sickle cell diseases and beta thalassemia major.
Comparison between Adult Patients with Sickle Cell Disease of Sub-Saharan African Origin Born in Metropolitan France and in Sub-Saharan Africa.
Comprehensive care for sickle cell disease immigrant patients: A reproducible model achieving high adherence to minimum standards of care.
Comprehensive, integrative management of pain for patients with sickle-cell disease.
Concerted global effort to combat sickle cell disease: the first global congress on sickle cell disease in Accra, Ghana.
Contribution of sickle cell disease to the pediatric stroke burden among hospital discharges of African-Americans-United States, 1997-2012.
Cooperative Study of Sickle Cell Disease: Demographic and socioeconomic characteristics of patients and families with sickle cell disease.
Costing model for neonatal screening and diagnosis of haemoglobinopathies.
Crises in Sickle Cell Disease.
Curative options for sickle cell disease: haploidentical stem cell transplantation or gene therapy?
Current management of sickle cell disease in pregnancy.
Current sickle cell disease management practices in Nigeria.
Depression and anxiety in adults with sickle cell disease: the PiSCES project.
Determination of the best method to estimate glomerular filtration rate from serum creatinine in adult patients with sickle cell disease: a prospective observational cohort study.
Developing a global agenda for sickle cell disease: report of an international symposium and workshop in Cotonou, Republic of Benin.
Dietary nonheme iron is equally bioavailable from ferritin or ferrous sulfate in thalassemia intermedia.
Disclosure and sickle cell disorder: A mixed methods study of the young person with sickle cell at school.
DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease.
Donor lymphocyte infusion to eradicate recurrent host hematopoiesis after allogeneic BMT for sickle cell disease.
Double whammy- acute splenic sequestration crisis in patient with aplastic crisis due to acute parvovirus infection.
Dural Venous Sinus Diameters in Children with Sickle Cell Disease: Correlation with History of Stroke in a Case-Control Study.
Earliest presenting sign and morbidity profile of sickle cell disease patients attending the adult SCD clinic at the UCH Ibadan, Nigeria.
Echocardiographic abnormalities in adolescent and adult Saudi patients with sickle cell disease.
Effect of Chronic Blood Transfusion on Biomarkers of Coagulation Activation and Thrombin Generation in Sickle Cell Patients at Risk for Stroke.
Effect of Extended-Release Niacin on Serum Lipids and on Endothelial Function in Adults With Sickle Cell Anemia and Low High-Density Lipoprotein Cholesterol Levels.
Effect of propranolol as antiadhesive therapy in sickle cell disease.
Effect of transfusion therapy on transcranial doppler ultrasonography velocities in children with sickle cell disease.
Effectiveness and safety of oral anticoagulants in patients with sickle cell disease and venous thromboembolism: a retrospective cohort study.
Effectiveness of surgical revascularization for stroke prevention in pediatric patients with sickle cell disease and moyamoya syndrome.
Electroencephalography hyperventilation and stroke in children with sickle cell disease.
Elevated homocysteine levels indicate suboptimal folate status in pediatric sickle cell patients.
Elevated urinary leukotriene E4 levels are associated with hospitalization for pain in children with sickle cell disease.
Emergence of ciprofloxacin resistance during treatment of Salmonella osteomyelitis in three patients with sickle cell disease.
Emergency Department (ED), ED Observation, Day Hospital, and Hospital Admissions for Adults with Sickle Cell Disease.
Empirically Derived Profiles of Health-Related Quality of Life in Youth and Young Adults with Sickle Cell Disease.
Endothelial cell NADPH oxidase mediates the cerebral microvascular dysfunction in sickle cell transgenic mice.
Endothelin receptor antagonists in sickle cell disease: A promising new therapeutic approach.
Estimated Life Expectancy and Income of Patients With Sickle Cell Disease Compared With Those Without Sickle Cell Disease.
Ethical Challenges in Hematopoietic Cell Transplantation for Sickle Cell Disease: a Review.
Evaluation of a density-based rapid diagnostic test for sickle cell disease in a clinical setting in zambia.
Evaluation of a Sickle Cell Disease Educational Website for Emergency Providers.
Evaluation of left ventricular diastolic function in pediatric sickle cell disease patients.
Evaluation of Serum Zinc and Antioxidant Vitamins in Adolescent Homozygous Sickle Cell Patients in Wardha, District of Central India.
Evidence-based interventions implemented in low-and middle-income countries for sickle cell disease management: A systematic review of randomized controlled trials.
Examining Biopsychosocial Factors in Relation to Multiple Pain Features in Pediatric Sickle Cell Disease.
Excess adenosine in murine penile erectile tissues contributes to priapism via A(2B) adenosine receptor signaling.
Exhaled carbon monoxide levels in children with sickle cell disease.
Factor V Leiden G1691A and prothrombin G20210A mutations among Palestinian patients with sickle cell disease.
Family Functioning, Medical Self-Management, and Health Outcomes Among School-Aged Children With Sickle Cell Disease: A Mediation Model.
Family Resilience From the Perspective of Caregivers of Youth With Sickle Cell Disease.
Fever Management in Sickle Cell Disease in Low- and Middle-Income Countries: A Survey of SCD Management Programs.
Foetal haemoglobin, erythrocytes containing foetal haemoglobin, and hematological features in congolese patients with sickle cell anaemia.
Folate supplementation in people with sickle cell disease.
Fracture prevalence and relationship to endocrinopathy in iron overloaded patients with sickle cell disease and thalassemia.
Free tissue transfer in patients with sickle cell disease: Considerations for multi-disciplinary peri-operative management.
Functional capacity in children and young adults with sickle cell disease undergoing evaluation for cardiopulmonary disease.
Gene coexpression networks analysis of sickle stroke risk.
Gene Therapy for ?-Hemoglobinopathies.
Gene-centric association study of acute chest syndrome and painful crisis in sickle cell disease patients.
Genome-wide association study of erythrocyte density in sickle cell disease patients.
Glomerular function in sickle cell disease patients during crisis.
Glutathione S-transferase gene polymorphisms (GSTM1, GSTT1, and GSTP1) in Egyptian pediatric patients with sickle cell disease.
Growing up with sickle cell disease: a pilot study of a transition program for adolescents with sickle cell disease.
Growth differentiation factor-15 in young sickle cell disease patients: relation to hemolysis, iron overload and vascular complications.
Haptoglobin gene polymorphisms in sickle cell disease patients with different ?S-globin gene haplotypes.
Headache in children with sickle cell disease: prevalence and associated factors.
Health related quality of life among adolescents with sickle cell disease in Saudi Arabia.
Health related quality of life and perception of stigmatisation in adolescents living with sickle cell disease in Nigeria: A cross sectional study.
Health-related Quality of Life in Children With Sickle Cell Disease Undergoing Chronic Red Cell Transfusion Therapy.
Heamostatic and genetic predisposing factors for stroke in children with sickle cell anemia.
Hematopoietic stem cells: potential new applications for translational medicine.
Hemin controls T cell polarization in sickle cell alloimmunization.
Hemoglobin and mean platelet volume predicts diffuse T1-MRI white matter volume decrease in sickle cell disease patients.
Hemoglobin Genotypes Modulate Inflammatory Response to Plasmodium Infection.
Hemostatic abnormalities in sickle cell disease.
Heterogeneity of respiratory disease in children and young adults with sickle cell disease.
High expression of the cGMP-specific phosphodiesterase, PDE9A, in sickle cell disease (SCD) and the effects of its inhibition in erythroid cells and SCD neutrophils.
Higher executive abilities following a blood transfusion in children and young adults with sickle cell disease.
Hydroxycarbamide exposure and ovarian reserve in women with sickle cell disease in the Multicenter Study of Hydroxycarbamide.
Hydroxyurea for the treatment of sickle cell disease.
Hydroxyurea improves nitric oxide bioavailability in humanized sickle cell mice.
Hypertrophic tonsils in sickle cell patients in ghana.
Hypoxia and inflammation in children with sickle cell disease: implications for hippocampal functioning and episodic memory.
iACT - An interactive mHealth monitoring system to enhance psychotherapy for adolescents with sickle cell disease.
Identification of genetic polymorphisms associated with risk for pulmonary hypertension in sickle cell disease.
Identification of the Ca(2+) entry pathway involved in deoxygenation-induced phosphatidylserine exposure in red blood cells from patients with sickle cell disease.
Immunoregulatory networks in sickle cell alloimmunization.
Impact of a Clinical Pharmacy Service on the Management of Patients in a Sickle Cell Disease Outpatient Center.
Impact of acute chest syndrome on lung function of children with sickle cell disease.
Impact of environmental tobacco smoke on children with sickle cell disease.
Impact of frontal white matter lesions on performance monitoring: ERP evidence for cortical disconnection.
Impact of long-term erythrocytapheresis on growth and peak height velocity of children with sickle cell disease.
Implications of a paediatrician-psychologist tandem for sickle cell disease care and impact on cognitive functioning.
Improved Guideline Adherence With Integrated Sickle Cell Disease and Asthma Care.
Improved survival of children and adolescents with sickle cell disease.
Improving the justice-based argument for conducting human gene editing research to cure sickle cell disease.
Incidence and predictors of hospital readmission in children presenting with severe anaemia in Uganda and Malawi: a secondary analysis of TRACT trial data.
Increased adhesive properties of platelets in sickle cell disease: roles for alphaIIb beta3-mediated ligand binding, diminished cAMP signalling and increased phosphodiesterase 3A activity.
Increased iron export by ferroportin induces restriction of HIV-1 infection in sickle cell disease.
Increased Red Blood Cell Stiffness Increases Pulmonary Vascular Resistance and Pulmonary Arterial Pressure.
Increased serum levels of anti-angiogenic factors soluble fms-like tyrosine kinase and soluble endoglin in sickle cell disease.
Influence of Nutrition on Disease Severity and Health-related Quality of Life in Adults with Sickle Cell Disease: A Prospective Study.
Inhibition of Band 3 tyrosine phosphorylation: a new mechanism for treatment of sickle cell disease.
Inhibition of Myeloperoxidase Decreases Vascular Oxidative Stress and Increases Vasodilatation in Sickle Cell Disease Mice.
Insights into elevated distortion product otoacoustic emissions in sickle cell disease: Comparisons of hydroxyurea-treated and non-treated young children.
Intense leuco-erythroblastic blood picture resembling erythro-leukaemia in sickle cell disease: a case report.
Intentional and unintentional nonadherence to hydroxyurea among people with sickle cell disease: a qualitative study.
Intestine-specific Disruption of Hypoxia-inducible Factor (HIF)-2? Improves Anemia in Sickle Cell Disease.
Invasive Pneumococcal Disease in Patients With Sickle Cell Disease.
Iron stores in pregnant women with sickle cell disease: a systematic review.
Is sickle cell disease sufficiently prioritized in policy and socio-economic research on diseases in Tanzania? Lessons for the past 50 years.
Is the incidence of appendicitis reduced in patients with sickle cell disease?
Jaundice in neonates with sickle cell disease. A case-control study.
Keys to Recruiting and Retaining Seriously Ill African Americans With Sickle Cell Disease in Longitudinal Studies: Respectful Engagement and Persistence.
Kidney function, urinalysis abnormalities and correlates in equatorial Africans with sickle cell disease.
Kidney Transplantation From a Donor With Sickle Cell Disease.
Knowledge and Health Beliefs Regarding Sickle Cell Disease Among Omanis in a Primary Healthcare Setting: Cross-sectional study.
Knowledge of sickle cell disease and haemoglobin electrophoresis: a survey of students of a tertiary institution.
Knowledge, attitude and practice of premarital counseling for sickle cell disease among youth in Yaba, Nigeria.
Knowledge, Experiences and Coping Mechanisms for Priapism among Persons with Sickle Cell Disease in Ibadan, Nigeria.
Language processing deficits in sickle cell disease in young school-age children.
Laparoscopic cholecystectomy in adult patients with sickle cell disease.
Let Their Voices Be Seen.
Levels of high-density lipoprotein cholesterol (HDL-C) among children with steady-state sickle cell disease.
Lipid profiles in French West Indies sickle cell disease cohorts, and their general population.
Lipoprotein subfraction profile and HDL-associated enzymes in sickle cell disease patients.
Liver transplantation in patients with sickle cell disease: possible but challenging-a cohort study.
Long Term Outcome and Evaluation of Organ Function in Pediatric Patients Undergoing Haploidentical and Matched Related Hematopoietic Cell Transplantation for Sickle Cell Disease.
Loss of Bone in Sickle Cell Trait and Sickle Cell Disease Female Mice Is Associated With Reduced IGF-1 in Bone and Serum.
Low exhaled nitric oxide and a polymorphism in the NOS I gene is associated with acute chest syndrome.
Measuring success: utility of biomarkers in sickle cell disease clinical trials and care.
Mechanisms of pain in sickle cell disease.
Morphological features of the human umbilical vein in normal, sickle cell trait, and sickle cell disease pregnancies.
Motivations and Decision-Making of Adult Sickle Cell Patients in High-Risk Clinical Research.
mTOR Inhibition Improves Anaemia and Reduces Organ Damage in a Murine Model of Sickle Cell Disease.
Multiple bone and joint diseases in a nigerian sickle cell anaemia: a case report.
Multiple primary choledocholithiasis in sickle cell disease.
Multiple transfusions for sickle cell disease in the Democratic Republic of Congo: The importance of the hepatitis C virus.
Multisystem damage associated with tricorporal priapism in sickle cell disease.
N-terminal pro-brain natriuretic peptide levels and risk of death in sickle cell disease.
Neurobiological mechanisms of pain in sickle cell disease.
Neurocognitive functioning in symptomatic adults with sickle cell disease: A description and comparison with unaffected siblings.
Neuropathic pain in patients with sickle cell disease.
Neuropathic pain is associated with poor health-related quality of life in adolescents with sickle cell disease: A preliminary report.
Newborn Screening for Sickle Cell Disease: Indian Experience.
Newborn screening for sickle cell disease: technical and legal aspects of a German pilot study with 38,220 participants.
Nocturnal enuresis and psychosocial problems in pediatric sickle cell disease and sibling controls.
Nocturnal enuresis in pediatric sickle cell disease.
Nocturnal oxyhemoglobin desaturation and arteriopathy in a pediatric sickle cell disease cohort.
Novel Metrics in the Longitudinal Evaluation of Pain Data in Sickle Cell Disease.
NT-pro brain natriuretic peptide levels and the risk of death in the cooperative study of sickle cell disease.
Objective Basis for Chronic Pain in Patients with Adult Sickle Cell Disease.
Obstetrician-gynecologists' knowledge of sickle cell disease screening and management.
Olinciguat, a stimulator of soluble guanylyl cyclase, attenuates inflammation, vaso-occlusion and nephropathy in mouse models of sickle cell disease.
Opioid selection during sickle cell pain crisis and its impact on the development of acute chest syndrome.
Optimal disease management and health monitoring in adults with sickle cell disease.
Outcomes, utilization, and costs among thalassemia and sickle cell disease patients receiving deferoxamine therapy in the United States.
Outpatient Pain Predicts Subsequent One-Year Acute Health Care Utilization Among Adults With Sickle Cell Disease.
Overcoming challenges of venous thromboembolism in sickle cell disease treatment.
Oxygen radical inhibition of nitric oxide-dependent vascular function in sickle cell disease.
Paediatric immunisation and chemoprophylaxis in a Ugandan sickle cell disease clinic.
Paediatric sickle cell disease: pulmonary hypertension but normal vascular resistance.
Pain Management Issues as Part of the Comprehensive Care of Patients with Sickle Cell Disease.
Parental attitudes toward research participation in pediatric sickle cell disease.
Parents of Children with Sickle Cell Disease Are Interested in Preimplantation Genetic Testing.
Pathologically stiff erythrocytes impede contraction of blood clots.
Patient reports of health outcome for adults living with sickle cell disease: development and testing of the ASCQ-Me item banks.
Patient satisfaction in specialized versus nonspecialized adult sickle cell care centers: the PiSCES study.
Patient-reported outcomes: descriptors of nociceptive and neuropathic pain and barriers to effective pain management in adult outpatients with sickle cell disease.
Patients' views on improving sickle cell disease management in primary care: focus group discussion.
Pattern and prevelence of alloimmunization in multiply transfused patients with sickle cell disease in Nigeria.
Pattern of Cerebral Blood Flow Velocity Using Transcranial Doppler Ultrasonography in Children with Sickle Cell Disorder in Lagos State, Nigeria.
PATTERNS OF LIVER IRON ACCUMULATION IN SICKLE CELL DISEASE AND THALASSAEMIA PATIENTS WITH IRON OVERLOAD.
Pediatric pain screening identifies youth at risk of chronic pain in sickle cell disease.
Pediatric residents' perceived barriers to opioid use in sickle cell disease pain management.
Pediatric to Adult Transition in Sickle Cell Disease: Survey Results from Young Adult Patients.
Perceptions and Practice of Early Diagnosis of Sickle Cell Disease by Parents and Physicians in a Southwestern State of Nigeria.
Perceptions of US Adolescents and Adults With Sickle Cell Disease on Their Quality of Care.
Periodic limb movement in sleep and sickle cell disease: a neglected association?
Photoacoustic Flow Cytometry for Single Sickle Cell Detection
Plasma glial fibrillary acidic protein levels in children with sickle cell disease.
Plasma levels of TNF-alpha in sickle cell patients receiving hydroxyurea.
Plasma Lipids and Lipoproteins in Sickle Cell Disease Patients in the Northern West Bank, Palestine.
Plasma protein C levels in children with sickle cell disease.
Pneumococcal and Meningococcal Vaccination among Michigan Children with Sickle Cell Disease.
Pneumococcal carriage among sickle cell disease patients in Accra, Ghana: Risk factors, serotypes and antibiotic resistance.
Prasugrel hydrochloride for the treatment of sickle cell disease.
Pregnancy outcomes in sickle cell disease: a retrospective cohort study from two tertiary centres in the UK.
Preliminary study of working memory in children with stroke related to sickle cell disease.
Prevalence and factors associated with renal dysfunction among children with sickle cell disease attending the sickle cell disease clinic at a tertiary hospital in Northwestern Tanzania.
Prevalence and incidence of congenital anomalies amongst babies born to women with sickle cell disease and exposed to hydroxyurea during pregnancy: a systematic review protocol.
Preventing Infections in Sickle Cell Disease: The Unfinished Business.
Providing Genetic Risk Information to Parents of Newborns with Sickle Cell Trait: Role of the General Practitioner in Neonatal Screening.
PspA family typing and PCR-based DNA fingerprinting with BOX A1R primer of pneumococci from the blood of patients in the USA with and without sickle cell disease.
Psychological Characteristics and Pain Frequency Are Associated With Experimental Pain Sensitivity in Pediatric Patients With Sickle Cell Disease.
Pulmonary function, CT and echocardiographic abnormalities in sickle cell disease.
Pulmonary functions in children and adolescents with sickle cell disease.
Quality of care in sickle cell disease: Cross-sectional study and development of a measure for adults reporting on ambulatory and emergency department care.
Quantitative Analysis of Extracranial Arterial Tortuosity in Patients with Sickle Cell Disease.
Quantitative MRI Analysis of Craniofacial Bone Marrow in Patients with Sickle Cell Disease.
Real-life experience with hydroxyurea in sickle cell disease: A multicenter study in a cohort of patients with heterogeneous descent.
Recommendations for the management of sickle cell disease in South Africa.
Regional oxygen extraction predicts border zone vulnerability to stroke in sickle cell disease.
Relationships between systemic vascular resistance, blood rheology and nitric oxide in children with sickle cell anemia or sickle cell-hemoglobin C disease.
Religious coping and the use of prayer in children with sickle cell disease.
Renal vascular resistance in sickle cell painful crisis.
Reproductive decisions in people with sickle cell disease or sickle cell trait.
Review of Sickle Cell Disease and Spinal Pathology.
Right ventricular and pulmonary function in sickle cell disease patients with pulmonary hypertension.
Risk of Asymptomatic Bacteriuria among People with Sickle Cell Disease in Accra, Ghana.
Rituximab for prevention of delayed hemolytic transfusion reaction in sickle cell disease.
Role for cAMP-protein kinase A signalling in augmented neutrophil adhesion and chemotaxis in sickle cell disease.
Safety and immunogenicity of heptavalent pneumococcal vaccine conjugated to CRM(197) among infants with sickle cell disease. Pneumococcal Conjugate Vaccine Study Group.
Seizures in the Jamaica cohort study of sickle cell disease.
Seizures risk factors in sickle cell disease. The cooperative study of sickle cell disease.
Self-management recommendations for sickle cell disease: A Ghanaian health professionals' perspective.
Self-perceived loss of control and untreated dental decay in African American adults with and without sickle cell disease.
Semisynthetic supra plasma expanders: a new class of therapeutics to improve microcircualtion in sickle cell anaemia.
Sensorineural hearing loss in adults with sickle cell anaemia.
Serum Immunoglobulin Levels in Children with Sickle Cell Disease: A Large Prospective Study.
Should young children with sickle cell disease and an available human leukocyte antigen identical sibling donor be offered hematopoietic cell transplantation?
Sickle cell anemia and hematological neoplasias.
Sickle cell disease and COVID-19: Susceptibility and severity.
Sickle Cell Disease and Perioperative Considerations: Review and Retrospective Report.
Sickle cell disease and pregnancy outcomes: population-based study on 8.8 million births.
Sickle Cell Disease Genomics of Africa (SickleGenAfrica) Network: ethical framework and initial qualitative findings from community engagement in Ghana, Nigeria and Tanzania.
Sickle cell disease in pregnancy. Obstetric and anesthetic management perspectives.
Sickle cell disease in pregnancy: maternal complications in a medicaid-enrolled population.
Sickle cell disease in sub-Saharan Africa: stakes and strategies for control of the disease.
Sickle cell disease in western Sudan: genetic epidemiology and predictors of knowledge attitude and practices.
Sickle cell disease--pathophysiology, clinical and diagnostic implications.
Sickle cell mutual assistance groups and the health services delivery system.
Sickle cell telemedicine and standard clinical encounters: a comparison of patient satisfaction.
Sickle cell trait diagnosis: clinical and social implications.
Silent brain infarcts are rare in Kuwaiti children with sickle cell disease and high Hb F.
Silent infarction as a risk factor for overt stroke in children with sickle cell anemia: a report from the Cooperative Study of Sickle Cell Disease.
Single-Incision Pediatric Endosurgery Cholecystectomy Performed by Residents in Children with Sickle Cell Disease.
Sleep patterns in pediatric sickle cell disease.
Sleep-disordered breathing and nocturnal hypoxemia in young adults with sickle cell disease.
Soluble P-selectin and vascular endothelial growth factor in steady state sickle cell disease: relationship to genotype.
Soluble receptor for advanced glycation end products as a vasculopathy biomarker in sickle cell disease.
Specifying sickle cell disease interventions: a study protocol of the Sickle Cell Disease Implementation Consortium (SCDIC).
Steady-state sVCAM-1 serum levels in adults with sickle cell disease.
Steroid treatment in children with sickle-cell disease.
Stigma and illness uncertainty: adding to the burden of sickle cell disease.
Stigma and Pain in Adolescents Hospitalized for Sickle Cell Vaso-occlusive Pain Episodes.
Stroke prevention and treatment in sickle cell disease.
Students' knowledge on sickle cell disease in Kisangani, Democratic Republic of the Congo.
Surfactant protein D as a marker for pulmonary complications in pediatric patients with sickle cell disease: Relation to lung function tests.
Survey of sickle cell disease in the Netherlands.
Survival among children and adults with sickle cell disease in Belgium: Benefit from hydroxyurea treatment.
Survival of children with sickle cell disease in the comprehensive newborn screening programme in Minas Gerais, Brazil.
Sustained long-term hematologic efficacy of hydroxyurea at maximum tolerated dose in children with sickle cell disease.
Systematic psychiatric assessment of patients with sickle cell disease.
Tardive hip disease diagnosis in a young adult with sickle cell disease.
Techniques for the Detection of Sickle Cell Disease: A Review.
Testing the Theory of Self-care Management for sickle cell disease.
The acute chest syndrome of sickle cell disease following aortic valve replacement.
The alpha-globin genotype does not influence sickle cell disease severity in a retrospective cross-validation study of the pediatric severity score.
The association of transfusion status with antioxidant enzymes and malondialdehyde level in Nigerians with sickle cell disease.
The CCR5?32 polymorphism in Brazilian patients with sickle cell disease.
The cost of health care for children and adults with sickle cell disease.
The DAU Allele and Anti-D Alloimmunization Present With High Frequency in Brazilian Sickle Cell Disease Patients.
The effect of dietary nitrate supplementation on the speed-duration relationship in mice with sickle cell disease.
The Effect of Hydroxyurea Therapy in Bahraini Sickle Cell Disease Patients.
The fatty acid composition of the serum phospholipids of children with sickle cell disease in Nigeria.
The features of sickle cell disease in Saudi children.
The Fucosylation Inhibitor, 2-Fluorofucose, Inhibits Vaso-Occlusion, Leukocyte-Endothelium Interactions and NF-?B Activation in Transgenic Sickle Mice.
The influence of infant and maternal sickle cell disease on birth outcome and neonatal course.
The interaction between sickle cell disease and HIV infection: a systematic review.
The platelet NLRP3 inflammasome is upregulated in sickle cell disease via HMGB1/TLR4 and Bruton tyrosine kinase.
The potential role of LSD1 inhibitors in the treatment of sickle cell disease: A review of preclinical animal model data.
The prevalence of abnormal leukocyte count, and its predisposing factors, in patients with sickle cell disease in Saudi Arabia.
The Prevalence of Uterine Fibroids in African American Women with Hemoglobin SS Sickle Cell Disease as Determined by Pelvic Magnetic Resonance Imaging.
The relation between regular outpatient follow-up and frequency of emergency department visits in sickle cell pediatric patients.
The Reliable, Automatic Classification of Neonates in First-Tier MALDI-MS Screening for Sickle Cell Disease.
The Sickle Cell Disease Ontology: Enabling Collaborative Research and Co-Designing of New Planetary Health Applications.
The use of neuropathic pain drugs in children with sickle cell disease is associated with older age, female sex, and longer length of hospital stay.
Thrombophilic mutations among Southern Iranian patients with sickle cell disease: high prevalence of factor V Leiden.
Transcranial color Doppler in stroke-free adult patients with sickle cell disease.
Transcranial Doppler ultrasonography in adults with sickle cell disease.
Transition from pediatric to adult care in sickle cell disease: establishing evidence-based practice and directions for research.
Tuberculosis in adult patients with sickle cell disease.
Twelve tips for teaching a comprehensive disease-focused course with a global perspective: A sickle cell disease example.
Understanding the Self-Management Practices of Young Adults with Sickle Cell Disease.
Understanding the social networks of parents of children with sickle cell disease.
Unmasking hypertension in children and adolescents with sickle/beta-thalassemia.
Update of hematopoietic cell transplantation for sickle cell disease.
Urinary Transforming Growth Factor ?-1 as a Marker of Renal Dysfunction in Sickle Cell Disease.
Utilising the 'Getting to Outcomes®' Framework in Community Engagement for Development and Implementation of Sickle Cell Disease Newborn Screening in Kaduna State, Nigeria.
Validation of the fine motor subtest of the Bayley-III with children with sickle cell disease using Rasch analysis.
Varied Age of First Presentation of Sickle Cell Disease: Case Presentations and Review.
Vaso-occlusive painful events in sickle cell disease: Impact on child well-being.
Venous thromboembolism in pregnant women with sickle cell disease: a retrospective database analysis.
Venous thromboembolism incidence in the Cooperative Study of Sickle Cell Disease.
Views of parents of children with sickle cell disease on pre-implantation genetic diagnosis.
Vitamin D and Nonskeletal Complications among Egyptian Sickle Cell Disease Patients.
Vitamin D level, lipid profile, and vitamin D receptor and transporter gene variants in sickle cell disease patients from Kurdistan of Iraq.
VLA-4 blockade by natalizumab inhibits sickle reticulocyte and leucocyte adhesion during simulated blood flow.
Voices of Adults Living with Sickle Cell Disease Pain.
Wheezing and asthma are independent risk factors for increased sickle cell disease morbidity.
Wheezing in children with sickle cell disease.
White Paper: Pathways to Progress in Newborn Screening for Sickle Cell Disease in Sub-Saharan Africa.
Will developments in allogeneic transplantation influence treatment of adult patients with sickle cell disease?
Xmn I polymorphic site in Yemeni sickle cell disease patients.
Youth with Sickle Cell Disease: Genetic and Sexual Health Education Needs.
[Neonatal screening for sickle cell disease in Nice University Hospital: Review of 8 last years].
[Neonatal screening of hemoglobinopathies and G6PD deficiency in Catalonia (Spain). Molecular study of sickle cell disease associated with alpha thalassemia and G6PD deficiency]
[Newborn screening for sickle cell disease in France].
[Progress in Gene Therapy of Sickle Cell Disease Based on Hemoglobin F--Review].
[Stroke prevention in sickle-cell disease: results, hurdles and future perspectives]
Aneurysm
Editor's Choice - Arteriotomy Closure Devices in EVAR, TEVAR, and TAVR: A Systematic Review and Meta-analysis of Randomised Clinical Trials and Cohort Studies.
Intracranial stenting as monotherapy in subarachnoid hemorrhage and sickle cell disease.
Nonaneurysmal Subarachnoid Hemorrhage in Sickle Cell Disease: Description of a Case and a Review of the Literature.
Normokinesia adjacent to left ventricular aneurysm: a differential risk for sudden cardiac death.
Preoperative selective intercostal angiography in patients undergoing thoracoabdominal aneurysm repair.
Prognostic role of left ventricular apical aneurysm in hypertrophic cardiomyopathy: A systematic review and meta-analysis.
Use of a flow-diverting stent for ruptured dissecting aneurysm treatment in a patient with sickle cell disease.
Ventricular Tachycardia Ablation Complicated with Ventricular Rupture.
[Risk assessment for development of sudden cardiac death in patients with progressive angina (based on results of 4-year prospective study)]
Aneurysm, Dissecting
Causes of sudden cardiac death in young athletes and non-athletes: systematic review and meta-analysis: Sudden cardiac death in the young.
Preoperative selective intercostal angiography in patients undergoing thoracoabdominal aneurysm repair.
Retrospective analysis of 769 cases of sudden cardiac death from 2006 to 2015: a forensic experience in China.
Sudden cardiac death from structural heart diseases in adults: imaging findings with cardiovascular computed tomography and magnetic resonance.
Angina Pectoris
Physical Activity and the Risk for Sudden Cardiac Death in Patients With Coronary Artery Disease.
Sudden cardiac death in patients with stable coronary artery disease and preserved left ventricular systolic function.
Angina, Unstable
Association of Testosterone Replacement With Cardiovascular Outcomes Among Men With Androgen Deficiency.
Estimating the incidence of the acute coronary syndrome: data from a Danish cohort of 138 290 persons.
Anosmia
Comparison of the clinical course of COVID-19 infection in sickle cell disease patients with healthcare professionals.
Anthrax
Suspected outbreak of cutaneous anthrax in Kasese district, the investigation and response, April to May 2007.
Antiphospholipid Syndrome
Atherothrombosis: environmental links.
Aortic Aneurysm, Abdominal
Hypertension Is a Risk Factor for Several Types of Heart Disease: Review of Prospective Studies.
Aortic Diseases
[Sudden cardiac death in women].
Aortic Rupture
Arrhythmogenic right ventricular cardiomyopathy and sudden cardiac death in young Koreans.
Sudden cardiac death in football players: Towards a new pre-participation algorithm.
Sudden cardiac death in young athletes; a literature review and special considerations in Asia.
Sudden cardiac death in young people with apparently normal heart.
Aortic Valve Insufficiency
Sudden cardiac death from structural heart diseases in adults: imaging findings with cardiovascular computed tomography and magnetic resonance.
Aortic Valve Stenosis
Arrhythmogenic right ventricular cardiomyopathy and sudden cardiac death in young Koreans.
Electrocardiograms in athletes: interpretation and diagnostic accuracy.
Pathophysiology and prevention of sudden cardiac death.
Appendicitis
Acute appendicitis in patients with sickle cell disease.
Acute Appendicitis in Pediatric Patients With Sickle Cell Disease: Lower Incidence, More Imaging, and More False-Positives.
Appendectomy during pregnancy in sickle cell disease patients.
Is acute appendicitis different in patients with sickle cell disease?
Is the incidence of appendicitis reduced in patients with sickle cell disease?
[Changes in the fat-acid spectrum of high-density lipoproteins as observed in men and women with acute appendicitis]
Arrhythmia, Sinus
Respiratory sinus arrhythmia as a predictor of sudden cardiac death after myocardial infarction.
Arrhythmias, Cardiac
12-lead electrocardiogram as a predictor of sudden cardiac death: from epidemiology to clinical practice.
A common co-morbidity modulates disease expression and treatment efficacy in inherited cardiac sodium channelopathy.
A comparison of genetic findings in sudden cardiac death victims and cardiac patients: the importance of phenotypic classification.
A contemporary assessment of the risk for sudden cardiac death in patients with congenital heart disease.
A multichannel decision-level fusion method for T wave alternans detection.
A novel cardiac ryanodine receptor gene (RyR2) mutation in an athlete with aborted sudden cardiac death: a case of adult-onset catecholaminergic polymorphic ventricular tachycardia.
A novel LMNA nonsense mutation causes two distinct phenotypes of cardiomyopathy with high risk of sudden cardiac death in a large five-generation family.
A potential role for integrin signaling in mechanoelectrical feedback.
A review of ECG and QT interval measurement use in a public psychiatric inpatient setting.
Aborted sudden cardiac death as first presentation of Wolff-Parkinson-White syndrome.
Acute effects of smoking on QT dispersion in healthy males.
Antipsychotic drugs and sudden cardiac death: A literature review of the challenges in the prediction, management, and future steps.
Arrhythmias and Sudden Cardiac Death in End Stage Renal Disease: Epidemiology, Risk Factors, and Management.
Arrhythmias and sudden cardiac death in post-cardiac transplant patients.
Arrhythmic events in Brugada syndrome patients induced by fever.
Arrhythmogenic mutation-linked defects in ryanodine receptor autoregulation reveal a novel mechanism of Ca2+ release channel dysfunction.
Assessing QT interval prolongation and its associated risks with antipsychotics.
Association of early repolarization and sudden cardiac death during an acute coronary event.
Association of QT dispersion with mortality and arrhythmic events-A meta-analysis of observational studies.
Associations of the serum long-chain omega-3 polyunsaturated fatty acids and hair mercury with heart rate-corrected QT and JT intervals in men: the Kuopio Ischaemic Heart Disease Risk Factor Study.
Asymptomatic Wolff-Parkinson-White Pattern ECG in USAF Aviators.
Calmodulinopathy: A Novel, Life-Threatening Clinical Entity Affecting the Young.
Cardiac arrest recorded on ambulatory electrocardiograms.
Cardiac arrhythmia and geomagnetic activity.
Cardiopulmonary complications leading to premature deaths in adult patients with sickle cell disease.
Cardiovascular complications in chronic dialysis patients.
Cardiovascular genomics and sudden cardiac death in the young.
Cardiovascular magnetic resonance-GUIDEd management of mild to moderate left ventricular systolic dysfunction (CMR GUIDE): Study protocol for a randomized controlled trial.
Catheter ablation to prevent sudden cardiac death.
Changes in BNP and QTc for prediction of sudden death in heart failure.
Characteristics and Clinical Significance of Late Gadolinium Enhancement by Contrast-Enhanced Magnetic Resonance Imaging in Patients with Hypertrophic Cardiomyopathy.
Chronically elevated branched chain amino acid levels are pro-arrhythmic.
Circular RNAs in Sudden Cardiac Death Related Diseases: Novel Biomarker for Clinical and Forensic Diagnosis.
Clinical trials of antiarrhythmic therapy--an improper answer to a proper question?
Clinical Utility of Microvolt T-wave Alternans Testing In Identifying Patients at High or Low Risk of Sudden Cardiac Death.
Common Genetic Variants Associated with Sudden Cardiac Death: The FinSCDgen Study.
Common genetic variants in sudden cardiac death.
Compression entropy contributes to risk stratification in patients with cardiomyopathy.
CRT-Pacemaker Versus CRT-Defibrillator Who Needs Sudden Cardiac Death Protection?
Current Perspectives on Sudden Cardiac Death in Hemodialysis Patients.
Distribution of ventricular fibrosis associated with life threatening ventricular tachyarrhythmias in patients with nonishcemic dilated cardiomyopathy.
Domperidone and ventricular arrhythmia or sudden cardiac death: a population-based case-control study in the Netherlands.
Domperidone safety: a mini-review of the science of QT prolongation and clinical implications of recent global regulatory recommendations.
Effect of atrioventricular conduction on heart rate variability.
Evaluation of patients with complex ventricular arrhythmias: current noninvasive and invasive methods.
Event and sideline management of sudden cardiac death.
Exercise-Associated Sudden Death in Finnish Standardbred and Coldblooded Trotters - A Case Series With Pedigree Analysis.
Focal Energy Deprivation Underlies Arrhythmia Susceptibility in Mice with Calcium-Sensitized Myofilaments.
Gender differences in ventricular arrhythmia recurrence in patients with coronary artery disease and implantable cardioverter-defibrillators.
Genetic Variants Associated With Unexplained Sudden Cardiac Death in Adult White and African American Individuals.
Genetics of sudden cardiac death syndromes.
Genomics in sudden cardiac death.
Genomics, heart failure and sudden cardiac death.
Heart rate is associated with markers of fatty acid desaturation: the GOCADAN study.
Heart rate turbulence and deceleration capacity for risk prediction of serious arrhythmic events in Marfan syndrome.
Hemodialysis-induced repolarization abnormalities on ECG are influenced by serum calcium levels and ultrafiltration volumes.
Hibernating myocardium: chronically adapted to ischemia but vulnerable to sudden death.
Hypertrophic Cardiomyopathy-Related Sudden Cardiac Death in Young People in Ontario.
Impact of cardiac rehabilitation on ventricular repolarization indexes in patients with rheumatid arthritis.
Implantable cardioverter defibrillator therapy for life-threatening arrhythmias in young patients.
Implantable cardioverter-defibrillator in Brugada syndrome: Long-term follow-up.
Importance of electrocardiographic markers in predicting cardiac events in children.
Inherited Arrhythmia Syndrome Predisposing to Sudden Cardiac Death.
Inherited primary arrhythmia disorders: cardiac channelopathies and sports activity.
Lambda-like ST-segment elevation in acute myocardial infarction triggered by coronary spasm may be a new risk predictor for lethal ventricular arrhythmia: A case report.
Late Gadolinium Enhancement and the Risk for Ventricular Arrhythmias or Sudden Death in Dilated Cardiomyopathy: Systematic Review and Meta-Analysis.
Life-threatening arrhythmias leading to syncope in patients with vasospastic angina.
Long-term incidence of malignant ventricular arrhythmia and shock therapy in patients with primary defibrillator implantation does not differ from event rates in patients treated for survived cardiac arrest.
Long-term subthreshold electrical stimulation of the left stellate ganglion and a canine model of sudden cardiac death.
Marine n-3 fatty acids, atrial fibrillation and QT interval in haemodialysis patients.
Masked inherited primary arrhythmia syndromes in sudden cardiac death patients accompanied by coronary vasospasm.
Mechanisms of sudden cardiac death.
Microvolt T wave alternans in adults with congenital heart diseases characterized by right ventricle pathology or single ventricle physiology: a case control study.
Microvolt T-wave alternans and autonomic nervous system parameters can be helpful in the identification of low-arrhythmic risk patients with ischemic left ventricular systolic dysfunction.
Modes of death and clinical outcomes in adult patients with hypertrophic cardiomyopathy in Thailand.
Molecular and genetic basis of sudden cardiac death.
Monitoring of arrhythmia and sudden death in a hemodialysis population: The CRASH-ILR Study.
Monogenec Arrhythmic Syndromes: From Molecular and Genetic Aspects to Bedside.
Myocardial ischemia and ventricular tachycardia on continuous electrocardiographic monitoring and risk of cardiovascular outcomes after non-ST-segment elevation acute coronary syndrome (from the MERLIN-TIMI 36 Trial).
New Approaches in the Management of Sudden Cardiac Death in Patients with Heart Failure-Targeting the Sympathetic Nervous System.
New perspectives on the role of autonomic nervous system in the genesis of arrhythmias.
Next-generation sequencing identified novel Desmoplakin frame-shift variant in patients with Arrhythmogenic cardiomyopathy.
Novel and Highly Lethal NKX2.5 Missense Mutation in a Family With Sudden Death and Ventricular Arrhythmia.
Novel KCNQ1 mutations in patients after myocardial infarction.
Optimal Medications and Appropriate Implantable Cardioverter-defibrillator Shocks in Aborted Sudden Cardiac Death Due to Coronary Spasm.
Out of hospital sudden cardiac death in Italy: a population-based case-control study.
Outcome after implantation of a cardioverter-defibrillator in patients with Brugada syndrome: a multicenter study.
Pathologic and electrocardiographic findings in sudden cardiac death in racehorses.
Pathophysiology and prevention of sudden cardiac death.
Patient Outcomes From a Specialized Inherited Arrhythmia Clinic.
Patients with coronary heart disease, dilated cardiomyopathy and idiopathic ventricular tachycardia share overlapping patterns of pathogenic variation in cardiac risk genes.
Pharmacotherapy in inherited and acquired ventricular arrhythmia in structurally normal adult hearts.
Phase statistics approach to human ventricular fibrillation.
Phobic anxiety and risk of coronary heart disease and sudden cardiac death among women.
Preclinical evidence for the therapeutic value of TBX5 normalization in arrhythmia control.
Predicting the risk of sudden cardiac death.
Prediction of sudden cardiac death after myocardial infarction in the beta-blocking era.
Prevalence of early repolarization pattern and its association with sudden cardiac death and arrhythmia over one-year follow-up in an Egyptian cohort.
Prevention of sudden cardiac death in patients with chronic kidney disease.
Primary prevention implantable cardioverter-defibrillator and opportunities for sudden cardiac death risk assessment in non-ischaemic cardiomyopathy.
Proarrhythmic risk and determinants of cardiac autonomic dysfunction in collagen-induced arthritis rats.
Protection from cardiac arrhythmia through ryanodine receptor-stabilizing protein calstabin2.
QTc-interval prolongation and increased risk of sudden cardiac death associated with hydroxychloroquine.
Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis.
Remote ischemic preconditioning differentially attenuates post-ischemic cardiac arrhythmia in streptozotocin-induced diabetic versus nondiabetic rats.
Repolarization abnormalities, arrhythmia and sudden death in canine tachycardia-induced cardiomyopathy.
Right single coronary artery as an incidental finding in Takotsubo syndrome and acute heart failure: Case report and review of the literature.
Right Ventricular Dysfunction and Long-Term Risk of Sudden Cardiac Death in Patients With and Without Severe Left Ventricular Dysfunction.
Right ventricular dysplasia: management and treatment in light of current evidence.
Risk factors for cardiac events in patients with Brugada syndrome: A PRISMA-compliant meta-analysis and systematic review.
Risk factors for sudden cardiac death in middle-aged British men.
Risk of arrhythmia induced by psychotropic medications: a proposal for clinical management.
Risk Stratification in Arrhythmogenic Right Ventricular Cardiomyopathy.
Role of CMR Imaging in Risk Stratification for Sudden Cardiac Death.
Role of nonsustained ventricular tachycardia and programmed ventricular stimulation for risk stratification in patients with idiopathic dilated cardiomyopathy.
RR-QT interval trend covariability for sudden cardiac death risk stratification.
Ryanodine receptor dysfunction in arrhythmia and sudden cardiac death.
Serum level of fibroblast growth factor 21 predicts long-term prognosis in patients with both diabetes mellitus and coronary artery calcification.
Short-term QT variability markers for the prediction of ventricular arrhythmias and sudden cardiac death: a systematic review.
Sickle cell disease-associated arrhythmias and in-hospital outcomes: Insights from the National Inpatient Sample.
Single nucleotide polymorphisms of SCN5A and SCN10A genes increase the risk of ventricular arrhythmias during myocardial infarction.
Sudden cardiac death after acute decompensation in heart failure patients: implications of discharge haemoglobin levels.
Sudden Cardiac Death and Arrhythmias.
Sudden cardiac death due to the Wolff-Parkinson-White syndrome: A case report with genetic analysis.
Sudden cardiac death from structural heart diseases in adults: imaging findings with cardiovascular computed tomography and magnetic resonance.
Sudden Cardiac Death in Athletes.
Sudden cardiac death in children and young adults without structural heart disease: a comprehensive review.
Sudden cardiac death in China: current status and future perspectives.
Sudden cardiac death in football players: Towards a new pre-participation algorithm.
Sudden Cardiac Death in Ischemic Heart Disease: From Imaging Arrhythmogenic Substrate to Guiding Therapies.
Sudden cardiac death in Long QT syndrome (LQTS), Brugada syndrome, and catecholaminergic polymorphic ventricular tachycardia (CPVT).
Sudden cardiac death in post myocardial infarction patients.
Sudden cardiac death risk factors in patients with heart failure treated with carvedilol.
Sudden cardiac death: A reappraisal.
Sudden cardiac death: from molecular biology and cellular electrophysiology to therapy.
Sudden cardiac death: The role of imaging.
Sudden death in athletes.
Sudden Death in Congenital Heart Disease: The Role of the Autopsy in Determining the Actual Cause.
Sympathetic Activation in Hypertensive Chronic Kidney Disease - A Stimulus for Cardiac Arrhythmias and Sudden Cardiac Death?
Sympathetic nerve sprouting, electrical remodeling and the mechanisms of sudden cardiac death.
The European Myocardial Infarct Amiodarone Trial (EMIAT). EMIAT Investigators.
The relationship between high resting heart rate and ventricular arrhythmogenesis in patients referred to ambulatory 24 h electrocardiographic recording.
The Role of the Cardioversion Defibrillator in Post Myocardial Infarction Sudden Cardiac Death: A Systematic Review of Clinical Trials and Observational Studies.
The spectrum of epidemiology underlying sudden cardiac death.
The Use of Implantable Cardioverter-defibrillators in the Prevention of Sudden Cardiac Death: A Focus on Congenital Heart Disease and Inherited Arrhythmia Syndromes.
Towards cardiac MRI based risk stratification in idiopathic dilated cardiomyopathy.
Traditional heart failure medications and sudden cardiac death prevention: a review.
Type 1 Brugada pattern electrocardiogram induced by hypokalemia.
Use of genetic testing to identify sudden cardiac death syndromes.
Use of wearable cardioverter-defibrillator in association with catheter ablation for atrial fibrillation-related tachycardiomyopathy.
Ventricular arrhythmia risk is associated with myocardial scar but not with response to cardiac resynchronization therapy.
Ventricular Arrhythmias in First Acute Myocardial Infarction: Epidemiology, Mechanisms, and Interventions in Large Animal Models.
Wearable cardioverter defibrillator: Bridge or alternative to implantation?
Whole-Exome Sequencing Identifies a Novel Mutation (p.L320R) of Alpha-Actinin 2 in a Chinese Family with Dilated Cardiomyopathy and Ventricular Tachycardia.
Wolff Parkinson white pattern in Danon disease: When preexcitation is not what it seems.
[Anesthesia for a patient with spinocerebellar degeneration who developed atrioventricular block]
[Application of molecular autopsy in sudden death caused by inherited arrhythmia].
[Immunohistochemical study of Cx43 dephosphorylation in human left ventricular myocardium suffered by acute ischemia]
[Implantable cardioverter-defibrillator in patients with chronic heart failure]
[Implanted cardioverters-defibrillators in the treatment of arrhythmias and prevention of sudden death]
[Prediction of inducible ventricular tachycardia by signal averaged electrocardiogram in patients with healed myocardial infarction]
[Sudden cardiac death : Epidemiology, pathophysiology and risk stratification].
[Sudden Cardiac Death in Patients With Chronic Obstructive Pulmonary Disease].
[The state and management of sudden death]
[Ultrastructure of subendocardial Purkinje cells and left-ventricular pseudotendons in sudden coronary death]
Arrhythmogenic Right Ventricular Dysplasia
Can sudden cardiac death in the young be predicted and prevented? Lessons from autopsy for the emergency physician.
Cardiac MRI and CT features of inheritable and congenital conditions associated with sudden cardiac death.
Catheter and Device Management of Inherited Cardiac Conditions.
Electrocardiograms in athletes: interpretation and diagnostic accuracy.
Exercise and Inherited Arrhythmias.
Exercise related sudden cardiac death (SCD) in the young - Pre-mortal characterization of a Swedish nationwide cohort, showing a decline in SCD among athletes.
Monogenec Arrhythmic Syndromes: From Molecular and Genetic Aspects to Bedside.
Monomorphic Ventricular Arrhythmias in Athletes.
Pathophysiology and prevention of sudden cardiac death.
Pitfalls in arrhythmogenic left ventricular cardiomyopathy (ALVC). A review of the literature with considerations on a single case of sudden death in a juvenile athlete.
Prevalence of arrhythmia-associated gene mutations and risk of sudden cardiac death in the Finnish population.
Sudden arrhythmia death syndrome in young victims: a five-year retrospective review and two-year prospective molecular autopsy study by next-generation sequencing and clinical evaluation of their first-degree relatives.
Sudden cardiac death in children and adolescents (excluding Sudden Infant Death Syndrome).
Sudden cardiac death in football players: Towards a new pre-participation algorithm.
Sudden cardiac death in nonischemic cardiomyopathy: Refining risk assessment.
Sudden cardiac death in patients with nonischemic cardiomyopathy.
Sudden cardiac death in young athletes; a literature review and special considerations in Asia.
Sudden cardiac death in young competitive athletes due to genetic cardiac abnormalities.
[Sudden cardiac death in athletes: is it always not preventable?].
[The ICD as primary prevention. Rare indications]
Arteriosclerosis
[Autopsy pathological characteristics in coronary artery disease patients with or without sudden cardiac death].
Arteriovenous Malformations
Treatment of a cerebral pial arteriovenous fistula in a patient with sickle cell disease-related moyamoya syndrome: case report.
Arthritis
Diagnostic and treatment difficulties in systemic lupus erythematosus coexisting with sickle cell disease.
Predictors of Subjective Cognitive Decline Among People With Diabetes: Data From the Behavioral Risk Factor Surveillance System.
Arthritis, Infectious
Multiple bone and joint diseases in a nigerian sickle cell anaemia: a case report.
Orthopaedic Manifestations of Sickle Cell Disease.
Septic arthritis in adults with sickle cell disease often is associated with osteomyelitis or osteonecrosis.
Arthritis, Rheumatoid
Cardiac arrhythmias and conduction disturbances in autoimmune rheumatic diseases.
Development and validation of SIMS: an instrument for measuring quality of life of adults with sickle cell disease.
Rheumatoid Arthritis in Sickle-Cell Population: Pathophysiologic Insights, Clinical Evaluation and Management.
Unusual sites of Salmonella osteoarthritis in patients with sickle cell disease: two cases.
Aspergillosis
Fatal case of cerebral aspergilloma complicated by ventriculitis and bacteremia due to Salmonella species in a sickle cell disease patient.
In vivo efficacy of a synthetic coumarin derivative in a murine model of aspergillosis.
Asthma
Acute pulmonary complications of sickle cell disease.
Adverse Reactions to Pneumococcal Vaccine in Pediatric and Adolescent Patients with Sickle Cell Disease.
Airway and alveolar nitric oxide production, lung function, and pulmonary blood flow in sickle cell disease.
Airway hyperreactivity is frequent in non-asthmatic children with sickle cell disease.
Airway Inflammation and Lung Function in Sickle Cell Disease.
Airway inflammation in sickle cell disease-A translational perspective.
Altered fatty acid metabolism and reduced stearoyl-coenzyme a desaturase activity in asthma.
Application of an Asthma Screening Questionnaire in Children with Sickle Cell Disease.
Asthma and acute chest in sickle-cell disease.
Asthma and sickle cell disease: two distinct diseases or part of the same process?
Asthma in children with sickle cell disease and its association with acute chest syndrome.
Asthma in children with sickle cell disease.
Asthma in sickle cell disease.
Asthma in the pediatric sickle cell patient with acute chest syndrome.
Asthma management in sickle cell disease.
Asthma management: reinventing the wheel in sickle cell disease.
Asthma morbidity and treatment in children with sickle cell disease.
Asthma Screening in Pediatric Sickle Cell Disease: A Clinic-Based Program Using Questionnaires and Spirometry.
Asthma, allergic sensitization and lung function in sickle cell disease.
Burden of influenza-related hospitalizations among children with sickle cell disease.
Chronic Pulmonary Complications of Sickle Cell Disease.
Cytokine levels and profiles in children related to sickle cell disease and asthma status.
Death due to asthma in two adolescents with sickle cell disease.
Dissatisfaction with hospital care for children with sickle cell disease not due only to race and chronic disease.
Drawings of Blood Cells Reveal People's Perception of Their Blood Disorder: A Pilot Study.
Effects of experimental asthma on inflammation and lung mechanics in sickle cell mice.
Elevated urinary leukotriene E4 levels are associated with hospitalization for pain in children with sickle cell disease.
Elevation of IgE in children with sickle cell disease is associated with doctor diagnosis of asthma and increased morbidity.
Elevation of tricuspid regurgitant jet velocity, a marker for pulmonary hypertension in children with sickle cell disease.
Family Engagement in Pediatric Sickle Cell Disease Visits.
Feasibility and preliminary outcomes of an integrated pediatric sickle cell disease and pulmonary care clinic for children with sickle cell disease.
Histopathology of experimentally induced asthma in a murine model of sickle cell disease.
Hospital admission for acute painful episode following methacholine challenge in an adolescent with sickle cell disease.
House Dust Mite-Induced Allergic Lung Inflammation Is Not Exacerbated in Sickle Cell Disease Mice.
Humoral and Cell-Mediated Immune Responses to Monovalent 2009 Influenza A/H1N1 and Seasonal Trivalent Influenza Vaccines in High-Risk Children.
Improved Guideline Adherence With Integrated Sickle Cell Disease and Asthma Care.
Improving Medication Adherence with Two-way Short Message Service Reminders in Sickle Cell Disease and Asthma. A feasibility randomized controlled trial.
Increased incidence of VTE in sickle cell disease patients: risk factors, recurrence and impact on mortality.
Inhaled Steroids Reduce Pain and sVCAM Levels in Individuals with Sickle Cell Disease: A Triple-Blind, Randomized Trial.
Intake of n-3 polyunsaturated fatty acids in childhood, FADS genotype and incident asthma.
Leukotriene pathway in sickle cell disease: a potential target for directed therapy.
Lung clearance index in children with sickle cell disease.
Maternal fatty acid desaturase genotype correlates with infant immune responses at 6 months.
Methacholine challenge in children with sickle cell disease: a case series.
Mortality, asthma, smoking and acute chest syndrome in young adults with sickle cell disease.
Painful episodes in children with sickle cell disease and asthma are temporally associated with respiratory symptoms.
Physician-diagnosed asthma and acute chest syndrome: associations with NOS polymorphisms.
Placenta growth factor augments airway hyperresponsiveness via leukotrienes and IL-13.
Psychosocial impact of sickle cell disease on mothers of affected children seen at University of Ilorin Teaching Hospital, Ilorin, Nigeria.
Pulmonary complications of sickle cell disease.
Pulmonary complications of sickle cell disease: a narrative clinical review.
Pulmonary Function Abnormalities and Asthma Are Prevalent in Children with Sickle Cell Disease and Are Associated with Acute Chest Syndrome.
Pulmonary hypertension in children and adolescents with sickle cell disease.
Pulmonary hypertension, tricuspid regurgitant velocity screening, and the nitric oxide pathway.
Recurrent, severe wheezing is associated with morbidity and mortality in adults with sickle cell disease.
Salbutamol Worsens the Autonomic Nervous System Dysfunction of Children With Sickle Cell Disease.
Sickle cell disease: wheeze or asthma?
Simulation of various randomization strategies for a clinical trial in sickle cell disease.
Spirometry use in Patients with Sickle Cell Disease with and without asthma and acute chest syndrome: A Multicenter Study.
Temporal relationship of asthma to acute chest syndrome in sickle cell disease.
Transition and sickle cell disease.
Urgency of Emergency Department Visits by Children With Sickle Cell Disease: A Comparison of 3 Chronic Conditions.
Validation of the breathmobile case identification survey for asthma screening in children with sickle cell disease.
Wheezing and asthma are independent risk factors for increased sickle cell disease morbidity.
Ataxia
Characteristics of the fastest isometric knee extension in patients with spinocerebellar degenerations.
Clinical and MRI Differences Between Patients With Subacute Combined Degeneration of the Spinal Cord Related vs. Unrelated to Recreational Nitrous Oxide Use: A Retrospective Study.
Difference in the Effects of Tandospirone on Ataxia in Various Types of Spinocerebellar Degeneration: An Open-Label Study.
Double-blind crossover study of branched-chain amino acid therapy in patients with spinocerebellar degeneration.
Glutamate dehydrogenase deficiency in spinocerebellar degenerations.
Hashimoto's Encephalopathy as a Treatable Adult-Onset Cerebellar Ataxia Mimicking Spinocerebellar Degeneration.
Impaired Adaptive Motor Learning Is Correlated With Cerebellar Hemispheric Gray Matter Atrophy in Spinocerebellar Ataxia Patients: A Voxel-Based Morphometry Study.
Influence of repetitive transcranial magnetic stimulation on disease severity and oxidative stress markers in the cerebrospinal fluid of patients with spinocerebellar degeneration.
Proceedings of a Sickle Cell Disease Ontology workshop - Towards the first comprehensive ontology for Sickle Cell Disease.
Quantitative analysis of upper-limb ataxia in patients with spinocerebellar degeneration.
Subacute combined degeneration without nutritional anemia.
Vestibular evoked myogenic potentials in patients with spinocerebellar degeneration.
[An MRI study of hereditary spinocerebellar degenerations]
[Brain stem auditory evoked potentials in spinocerebellar degeneration]
[Study on argyrophilic inclusions of multisystem atrophy (Oppenheimer)]
[The Nomenclature and Classification of Sporadic Spinocerebellar Degeneration].
Ataxia Telangiectasia
The expression of genes related to adipocyte differentiation in pigs.
Atherosclerosis
A common SCN5A variant is associated with PR interval and atrial fibrillation among African Americans.
A statistical study of sudden cardiac death for past five years in Osaka medical, investigated at the Osaka Medical Examiner's Office.
Absence of stearoyl-CoA desaturase-1 does not promote DSS-induced acute colitis.
Cardiomegaly is a common arrhythmogenic substrate in adult sudden cardiac deaths, and is associated with obesity.
Carotid Intima-Media Thickness and the Risk of Sudden Cardiac Death: The ARIC Study and the CHS.
Clinical characteristics and long-term prognosis of spontaneous coronary artery dissection: A single-center Chinese experience.
Clinical Predictive Value of Cystatin C in Pediatric Sickle Cell Disease: A Marker of Disease Severity and Subclinical Cardiovascular Dysfunction.
Combined Therapy of Dietary Fish Oil and Stearoyl-CoA Desaturase 1 Inhibition Prevents the Metabolic Syndrome and Atherosclerosis.
Coronary Artery Disease as the Cause of Sudden Cardiac Death Among Victims < 50 Years of Age.
Despite antiatherogenic metabolic characteristics, SCD1-deficient mice have increased inflammation and atherosclerosis.
Distinct regulation of stearoyl-CoA desaturase 1 gene expression by cis and trans C18:1 fatty acids in human aortic smooth muscle cells.
Dyslipidemia and atherosclerosis induced by chronic intermittent hypoxia are attenuated by deficiency of stearoyl coenzyme A desaturase.
Effects of Bacillus polyfermenticus SCD on lipid and antioxidant metabolisms in rats fed a high-fat and high-cholesterol diet.
Effects of conjugated linoleic acid (CLA) on immune responses, body composition and stearoyl-CoA desaturase.
Electrocardiographic and clinical predictors separating atherosclerotic sudden cardiac death from incident coronary heart disease.
Fatty Acid Bile Acid Conjugate Inhibits Hepatic Stearoyl Coenzyme A Desaturase and Is Non-atherogenic.
Fatty acid composition and estimated desaturase activities are associated with obesity and lifestyle variables in men and women.
Genetic variations in nitric oxide synthase 1 adaptor protein are associated with sudden cardiac death in US white community-based populations.
Imaging of hypoxia in mouse atherosclerotic plaques with (64)Cu-ATSM.
Inhibition of stearoyl-coenzyme A desaturase 1 dissociates insulin resistance and obesity from atherosclerosis.
Intake of total trans, trans-18:1, and trans-18:2 fatty acids and risk of sudden cardiac death in women.
Novel substituted heteroaromatic compounds as inhibitors of stearoyl-CoA desaturase.
Paradoxical protection from atherosclerosis and thrombosis in a mouse model of sickle cell disease.
Plasma chitotriosidase and carotid intima-media thickness in children with sickle cell disease.
Plasma remnant-like lipoprotein particles or LDL-C as major pathologic factors in sudden cardiac death cases.
Potential role of LPS in the outcome of Helicobacter pylori related diseases.
Pre-germinated brown rice extract ameliorates high-fat diet-induced metabolic syndrome.
Predictors of sudden cardiac death in atrial fibrillation: The Atherosclerosis Risk in Communities (ARIC) study.
Prospective study of sudden cardiac death among women in the United States.
Proteomic identification of altered apolipoprotein patterns in pulmonary hypertension and vasculopathy of sickle cell disease.
Regulation of stearoyl-CoA desaturase expression.
Relation of atrial and/or ventricular premature complexes on a two-minute rhythm strip to the risk of sudden cardiac death (the Atherosclerosis Risk in Communities [ARIC] study).
Relation of Prolonged P-Wave Duration to Risk of Sudden Cardiac Death in the General Population (from the Atherosclerosis Risk in Communities Study).
SCD rs41290540 single-nucleotide polymorphism modifies miR-498 binding and is associated with a decreased risk of coronary artery disease.
Sodium Orthovanadate Changes Fatty Acid Composition and Increased Expression of Stearoyl-Coenzyme A Desaturase in THP-1 Macrophages.
Sudden Cardiac Death in Young Adults: Environmental Risk Factors and Genetic Aspects of Premature Atherosclerosis*(,) †
Sudden Cardiac Death Risk Distribution in the United States Population (from NHANES, 2005 to 2012).
Toll-like receptor signaling links dietary fatty acids to the metabolic syndrome.
[Impact of Myocardial Infarction and Abnormalities of Cardiac Conduction System on Sudden Cardiac Death].
[Lipid, lipoproteins and atherogenesis profiles in sickle cell disease among Central African patients].
[Pathomorphologic study of the fibrous cap and fatty core of coronary Anthrosclerotic plaque in sudden coronary death]
[Sudden cardiac death in diabetes mellitus].
[Sudden cardiac death: state of the art]
Atrial Fibrillation
Arrhythmogenic right ventricular cardiomyopathy: ECG progression over time and correlation with long-term follow-up.
Association of sickle cell trait with atrial fibrillation: The REGARDS cohort.
Atrial fibrillation and risk of major arrhythmic events in Brugada syndrome: A meta-analysis.
Cardiorespiratory fitness and heart rate recovery predict sudden cardiac death independent of ejection fraction.
Competing risk analysis of cause-specific mortality in patients with an implantable cardioverter-defibrillator: The EVADEF cohort study.
Depression and Risk of Sudden Cardiac Death and Arrhythmias: A Meta-Analysis.
Determinants of Sudden Cardiac Death in Adult Patients With Eisenmenger Syndrome.
Hypertension Is a Risk Factor for Several Types of Heart Disease: Review of Prospective Studies.
Mechanism and prediction of sudden cardiac death in arrhythmia patients using electrophysiological studies.
Modes of death and clinical outcomes in adult patients with hypertrophic cardiomyopathy in Thailand.
Pre-participation and follow-up screening of athletes for endurance sport.
Predictors of sudden cardiac death change with time after myocardial infarction: results from the VALIANT trial.
Predictors of sudden cardiac death in high-risk patients following a myocardial infarction.
QT prolongation and sudden cardiac death risk in hypertrophic cardiomyopathy.
Racial differences in sudden cardiac death among hypertensive patients during antihypertensive therapy: The LIFE study.
Regression of electrocardiographic left ventricular hypertrophy during antihypertensive therapy and reduction in sudden cardiac death: the LIFE Study.
Relation of Prolonged P-Wave Duration to Risk of Sudden Cardiac Death in the General Population (from the Atherosclerosis Risk in Communities Study).
Risk Factor and Prediction Modeling for Sudden Cardiac Death in Women With Coronary Artery Disease.
Risk Markers and Appropriate Implantable Defibrillator Therapy in Hypertrophic Cardiomyopathy.
Short QT syndrome.
Sickle cell disease-associated arrhythmias and in-hospital outcomes: Insights from the National Inpatient Sample.
Sudden Cardiac Death in Patients With Atrial Fibrillation: Insights From the ENGAGE AF-TIMI 48 Trial.
Sudden cardiac death risk factors in patients with heart failure treated with carvedilol.
The relationship between the quantitative extent of late gadolinium enhancement and burden of nonsustained ventricular tachycardia in hypertrophic cardiomyopathy: A delayed contrast-enhanced magnetic resonance study.
Thyroid-stimulating hormone and risk of sudden cardiac death, total mortality and cardiovascular morbidity.
[Heart failure and mortality: polyunsaturated fatty acids and the relevance of evidence].
Atrial Flutter
A 34-year longitudinal study on long-term cardiac outcomes in DM1 patients with normal ECG at baseline at an Italian clinical centre.
Mechanism and prediction of sudden cardiac death in arrhythmia patients using electrophysiological studies.
Atrioventricular Block
A Novel Risk Stratification Score for Sudden Cardiac Death Prediction in Middle-Aged, Nonischemic Dilated Cardiomyopathy Patients: The ESTIMATED Score.
Brugada syndrome in the young: an assessment of risk factors predicting future events.
Cardiac arrest recorded on ambulatory electrocardiograms.
Clinical Impact of Baseline Right Bundle Branch Block in Patients Undergoing Transcatheter Aortic Valve Replacement.
Long-term subthreshold electrical stimulation of the left stellate ganglion and a canine model of sudden cardiac death.
Nerve sprouting and sudden cardiac death.
QT prolongation and sudden cardiac death risk in hypertrophic cardiomyopathy.
Sudden death in cardiac sarcoidosis: an analysis of nationwide clinical and cause-of-death registries.
Auditory Diseases, Central
The evaluation of auditory function in homozygous sickle cell disease.
Autoimmune Diseases
Partial dysfunction of Treg activation in sickle cell disease.
Systemic lupus erythematosus in patients with sickle cell disease.
Avitaminosis
Nutritional deficiencies in iron overloaded patients with hemoglobinopathies.
Azoospermia
Gonadal function of young adults after therapy of malignancies during childhood or adolescence.
Sperm DNA fragmentation levels in testicular sperm samples from azoospermic males as assessed by the sperm chromatin dispersion (SCD) test.
Successful fertility restoration after allogeneic hematopoietic stem cell transplantation.
Babesiosis
Robust adaptive immune response against Babesia microti infection marked by low parasitemia in a murine model of sickle cell disease.
Bacteremia
Bacteremia risk and outpatient management of febrile patients with sickle cell disease.
Bacterial blood cultures in children with sickle cell disease.
Ceftriaxone-resistant Salmonella septicemia and osteomyelitis in sickle cell disease adults.
Fever in children with sickle cell disease: are all fevers equal?
Frequency of bacteremia in patients with sickle cell disease: a longitudinal study.
Incidence of invasive Haemophilus influenzae infections in children with sickle cell disease.
Invasive Pneumococcal Disease in Patients With Sickle Cell Disease.
Low-risk factors for severe bacterial infection and acute chest syndrome in children with sickle cell disease.
Plasma Folate Levels in Acutely Ill and Steady State Pediatric Sickle Cell Disease Patients in Ghana.
Predictors of Bacteremia Among Children With Sickle Cell Disease Presenting With Fever.
Predictors of bacteremia in febrile children with sickle cell disease.
Prevalence and Etiology of Bacteremia in Febrile Children with Sickle Cell Disease at a Nigeria Tertiary Hospital.
Prevalence of Bacteremia in Febrile Patients With Sickle Cell Disease: Meta-Analysis of Observational Studies.
Streptococcus pneumoniae sepsis and meningitis during the penicillin prophylaxis era in children with sickle cell disease.
[Infectious complications after surgical splenectomy in children with sickle cell anemia disease].
Bacterial Infections
A Standardized Clinical Pathway to Decrease Hospital Admissions Among Febrile Children With Sickle Cell Disease.
A Toll-like receptor 2 genetic variant modulates occurrence of bacterial infections in patients with sickle cell disease.
Bordetella holmesii bacteremia in sickle cell disease.
Burden and spectrum of bacterial infections among sickle cell disease children living in Cameroon.
Children with sickle cell disease and human immunodeficiency virus-1 infection: use of inpatient care services in the United States.
Effect of active prenatal management on pregnancy outcome in sickle cell disease in an African setting.
How we prevent and manage infection in sickle cell disease.
Incidence and predictors of bacterial infections in febrile children with sickle cell disease.
Infections and sickle cell disease in Eastern Saudi Arabian children.
Interleukin 6 as a marker of severe bacterial infection in children with sickle cell disease and fever: a case-control study.
Low-risk factors for severe bacterial infection and acute chest syndrome in children with sickle cell disease.
Morbidity and pregnancy outcomes associated with sickle cell anemia among Saudi women.
Population Pharmacokinetics of Cefotaxime and Dosage Recommendations in Children with Sickle Cell Disease.
Red blood cells, platelets and polymorphonuclear neutrophils of patients with sickle cell disease exhibit oxidative stress that can be ameliorated by antioxidants.
Significance of electronic health records: A comparative study of vaccination rates in patients with sickle cell disease.
Th1 and Th2 cytokine profiles in sickle cell disease.
The anaerobic and aerobic bacterial flora of leg ulcers in patients with sickle-cell disease.
Bacteriuria
Comparison of a new system (Compactdry SCD) with conventional methods for quantitative urine cultures.
Bartonella Infections
Prevalence of Bartonella spp. Infection in Patients with Sickle Cell Disease.
beta-Thalassemia
A literature review on the parvovirus B19 infection in sickle cell anemia and ?-thalassemia patients.
A Rare Cause of Chronic Liver Disease Diagnosed by Endoscopic Ultrasound-Guided Liver Biopsy.
Bone marrow transplantation in sickle cell anemia.
Cardiac iron load and function in transfused patients treated with deferasirox (the MILE study).
Comparative evaluation of oral and dento-maxillofacial manifestation of patients with sickle cell diseases and beta thalassemia major.
Comparison of organ dysfunction in transfused patients with SCD or beta thalassemia.
Consequences and management of iron overload in sickle cell disease.
Dietary nonheme iron is equally bioavailable from ferritin or ferrous sulfate in thalassemia intermedia.
Dispersion of repolarization and beta-thalassemia major: the prognostic role of QT and JT dispersion for identifying the high-risk patients for sudden death.
DNA hypomethylation therapy for hemoglobin disorders: molecular mechanisms and clinical applications.
Doppler Assessment of Renal Hemodynamic Alterations in Homozygous Sickle Cell Disease and Sickle Beta-Thalassemia.
Extramedullary Hematopoiesis in the Sinonasal Cavity: A Case Report and Review of the Literature.
Genetic modulators of sickle cell disease in French Guiana: Markers of the slave trade.
Hemosiderosis causing liver cirrhosis in a patient with Hb S/beta thalassemia and no other known causes of hepatic disease.
Hidden brain iron content in sickle cell disease: impact on neurocognitive functions.
Hypercoagulability in sickle cell disease and beta-thalassemia.
Identification of a PRMT5-dependent repressor complex linked to silencing of human fetal globin gene expression.
Increased Rates of Rhabdomyolysis in Male Hematopoietic Cell Transplantation Recipients Taking Sirolimus and Trimethoprim/Sulfamethoxazole.
Integrated automated particle tracking microfluidic enables high-throughput cell deformability cytometry for red cell disorders.
Late Effects Screening Guidelines after Hematopoietic Cell Transplantation (HCT) for Hemoglobinopathy: Consensus Statement from the Second Pediatric Blood and Marrow Transplant Consortium International Conference on Late Effects after Pediatric HCT.
New approach to accurate interpretation of sickle cell disease newborn screening by applying multiple of median cutoffs and ratios.
Quantification of HBG mRNA in primary erythroid cultures: prediction of the response to hydroxyurea in sickle cell and beta-thalassemia.
Selenium and Vitamin E as antioxidants in chronic hemolytic anemia: Are they deficient? A case-control study in a group of Egyptian children.
Serum zinc levels and zinc binding capacity in thalassemia.
Sickle cell disease and pregnancy in Bahrain.
Sickle-cell nephropathy: MR imaging.
Successful Treatment of Hepatitis C Virus by Ledipasvir/Sofosbuvir in a Cirrhotic Patient with Sickle Cell Disease and Thalassemia Minor.
Sustained long-term hematologic efficacy of hydroxyurea at maximum tolerated dose in children with sickle cell disease.
Synergistic Effect of Simvastatin and Romidepsin on Gamma-globin Gene Induction.
The effect of hydroxyurea on the coagulation system in sickle cell anemia and beta-thalassemia intermedia patients: a preliminary study.
[S hemoglobinopathies in Argentina]
Bicuspid Aortic Valve Disease
Role of echocardiography in screening and evaluation of athletes.
Blindness
Ocular manifestations of sickle cell disease.
Blister
Secondary ciliary dyskinesia is absent after ciliogenesis in culture.
Bone Diseases
Complete resolution of sickle cell chronic pain with high dose vitamin D therapy: a case report and review of the literature.
Development of Algorithm for Clinical Management of Sickle Cell Bone Disease: Evidence for a Role of Vertebral Fractures in Patient Follow-up.
Hypoxia-reperfusion affects osteogenic lineage and promotes sickle cell bone disease.
MiR-1908/EXO1 and MiR-203a/FOS, regulated by scd1, are associated with fracture risk and bone health in postmenopausal diabetic women.
Response to Long-term Vitamin D Therapy for Bone Disease in Children With Sickle Cell Disease.
Sickle cell disease promotes sex-dependent pathological bone loss through enhanced cathepsin proteolytic activity.
Tartrate-Resistant Acid Phosphatase 5b in Young Patients With Sickle Cell Disease and Trait Siblings: Relation to Vasculopathy and Bone Mineral Density.
Bone Diseases, Metabolic
Evaluation of panoramic radiomorphometric indices related to low bone density in sickle cell disease.
High prevalence and correlates of low bone mineral density in young adults with sickle cell disease.
Mechanisms of Bone Impairment in Sickle Bone Disease.
Predictors of abnormal bone mass density in adult patients with homozygous sickle-cell disease.
Prevalence and Clinical Characteristics of Rheumatoid Arthritis in an Inner City Population with Sickle Cell Disease.
Secondary osteoporosis due to sickle cell anemia: Do sex steroids play a role?
Sickle cell disease promotes sex-dependent pathological bone loss through enhanced cathepsin proteolytic activity.
Bone Resorption
Assessment of the bone status of Nigerian children and adolescents with sickle cell disease using calcaneal ultrasound and serum markers of bone metabolism.
Cranial thickness in superior canal dehiscence syndrome: implications for canal resurfacing surgery.
Sickle cell bone disease: response to vitamin D and calcium.
Sickle cell diseases: What can nuclear medicine offer?
Bradycardia
Acute restraint stress provokes sudden cardiac death in normotensive rats and enhances susceptibility to arrhythmogenic effects of adrenaline in spontaneously hypertensive rats.
Arrhythmias and Sudden Cardiac Death in End Stage Renal Disease: Epidemiology, Risk Factors, and Management.
Cardiac arrest recorded on ambulatory electrocardiograms.
Continuous telemetry from a chronic canine model of sudden cardiac death.
Current Perspectives on Sudden Cardiac Death in Hemodialysis Patients.
Future bradyarrhythmia in patients with hypertrophic cardiomyopathy.
Heart rhythm at the time of death documented by an implantable loop recorder.
Mechanisms of sudden cardiac death.
Monitoring of arrhythmia and sudden death in a hemodialysis population: The CRASH-ILR Study.
Pathology of the myocardium and the conduction system in sudden coronary death.
Prediction of sudden death in elderly patients with heart failure.
Profiling risk from arrhythmic or hemodynamic death.
QT prolongation and sudden cardiac death risk in hypertrophic cardiomyopathy.
Role of risk stratification and genetics in sudden cardiac death.
Subcutaneous implantable cardioverter-defibrillator implantation for ventricular fibrillation caused by coronary artery spasm: a case report.
Sudden cardiac death and tuberculosis - How much do we know?
Sudden cardiac death preceded by ST segment elevations during ECG patch monitoring.
Temporal distribution of arrhythmic events in chronic kidney disease: Highest incidence in the long interdialytic period.
The clinical challenge of preventing sudden cardiac death immediately after acute ST-elevation myocardial infarction.
[Non-pharmacologic prevention of sudden cardiac death]
[Sudden cardiac death and automated external defibrillators. Where we are in 2012?].
[Worldwide experience with automated external defibrillators : What have we achieved? What else can we expect?].
Brain Abscess
Salmonella enteritidis brain abscess in a sickle cell disease patient: case report and review of the literature.
Brain Death
Experience in renal and extrarenal transplantation with donation after cardiac death donors with selective use of extracorporeal support.
Brain Diseases
Chronic progressive spinocerebellar syndrome associated with antibodies to human T-lymphotropic virus type I: clinico-virological and magnetic resonance imaging studies.
Neurologic complications in children under five years with sickle cell disease.
Nonaneurysmal Subarachnoid Hemorrhage in Sickle Cell Disease: Description of a Case and a Review of the Literature.
Brain Infarction
Discontinuing prophylactic transfusions increases the risk of silent brain infarction in children with sickle cell disease: data from STOP II.
HLA-DRB1 alleles in Hb SS patients with avascular necrosis of the femoral head.
Recurrent large volume silent strokes in sickle cell disease.
Brain Injuries
Brain imaging findings in pediatric patients with sickle cell disease.
Cognitive and behavioral function in children with sickle cell disease: a review and discussion of methodological issues.
Graph Lasso-Based Test for Evaluating Functional Brain Connectivity in Sickle Cell Disease.
Hematopoietic stem cell transplantation reverses white matter injury measured by diffusion-tensor imaging (DTI) in sickle cell disease patients.
Neurologic complications of sickle cell disease.
Plasma glial fibrillary acidic protein levels in children with sickle cell disease.
Proteomic discovery in sickle cell disease: Elevated neurogranin levels in children with sickle cell disease.
Brain Injuries, Traumatic
Subjective Cognitive Decline and Related Cognitive Deficits.
Brain Ischemia
Circadian influence on coronary events.
Enriched endogenous omega-3 fatty acids in mice protect against global ischemia injury.
Plasma glial fibrillary acidic protein levels in children with sickle cell disease.
The expression of '150-kDa oxygen regulated protein (ORP-150)' in human brain and its relationship with duration time until death.
Brain Neoplasms
Enoxaparin increases the incidence of postoperative intracranial hemorrhage when initiated preoperatively for deep venous thrombosis prophylaxis in patients with brain tumors.
Breast Neoplasms
17?-estradiol induces stearoyl-CoA desaturase-1 expression in estrogen receptor-positive breast cancer cells.
Breast cancer in patients with sickle cell disease can be treated safely with weekly paclitaxel.
Correction: Human Breast Cancer Tissues Contain Abundant Phosphatidylcholine(36?1) with High Stearoyl-CoA Desaturase-1 Expression.
Decreasing stearoyl-CoA desaturase-1 expression inhibits ?-catenin signaling in breast cancer cells.
Effects of adenoviral gene transfer of C. elegans n-3 fatty acid desaturase on the lipid profile and growth of human breast cancer cells.
Fatty Acid Composition of Tissue Cultured Breast Carcinoma and the Effect of Stearoyl-CoA Desaturase 1 Inhibition.
Gene transfer of Chlorella vulgaris n-3 fatty acid desaturase optimizes the fatty acid composition of human breast cancer cells.
High stearoyl-CoA desaturase 1 expression is associated with shorter survival in breast cancer patients.
Human breast cancer tissues contain abundant phosphatidylcholine(36?1) with high stearoyl-CoA desaturase-1 expression.
Inhibition of stearoyl-CoA desaturase activity by the cis-9,trans-11 isomer and the trans-10,cis-12 isomer of conjugated linoleic acid in MDA-MB-231 and MCF-7 human breast cancer cells.
Metabolic Effect of Estrogen Receptor Agonists on Breast Cancer Cells in the Presence or Absence of Carbonic Anhydrase Inhibitors.
Novel theranostic opportunities offered by characterization of altered membrane lipid metabolism in breast cancer progression.
Paclitaxel-induced sickle cell crisis.
Pivotal role of human stearoyl-CoA desaturases (SCD1 and 5) in breast cancer progression: oleic acid-based effect of SCD1 on cell migration and a novel pro-cell survival role for SCD5.
Rapamycin regulates stearoyl CoA desaturase 1 expression in breast cancer.
Risk of secondary lymphedema in breast cancer survivors is related to serum phospholipid fatty acid desaturation.
SCD1 activity promotes cell migration via a PLD-mTOR pathway in the MDA-MB-231 triple-negative breast cancer cell line.
Stearoyl-CoA desaturase 1 and paracrine diffusible signals have a major role in the promotion of breast cancer cell migration induced by cancer-associated fibroblasts.
Stearoyl-CoA desaturase-1, a novel target of omega-3 fatty acids for reducing breast cancer risk in obese postmenopausal women.
Suppression of Nuclear Factor-?B by Glucocorticoid Receptor Blocks Estrogen-Induced Apoptosis in Estrogen-Deprived Breast Cancer Cells.
The fatty acid desaturation index of blood lipids, as a biomarker of hepatic stearoyl-CoA desaturase expression, is a predictive factor of breast cancer risk.
The Health Deviation of Post-Breast Cancer Lymphedema: Symptom Assessment and Impact on Self-Care Agency.
Transcriptome profiling revealed multiple genes and ECM-receptor interaction pathways that may be associated with breast cancer.
Transcriptomic profiling of curcumin-treated human breast stem cells identifies a role for stearoyl-coa desaturase in breast cancer prevention.
Tumor-Associated Stromal Cellular Density as a Predictor of Recurrence and Mortality in Breast Cancer: Results from Ethnically Diverse Study Populations.
[Inhibition of SCD1 Activity Blocks Cell Cycle Progression and Impairs Proliferation in Breast Cancer Cells].
Bronchial Diseases
Progression and Prognostic Indicators of Bronchial Disease in Children with Sickle Cell Disease.
Bronchial Hyperreactivity
Asthma in children with sickle cell disease and its association with acute chest syndrome.
Bronchiolitis Obliterans
Allogeneic hematopoietic stem cell transplantation in congenital hemoglobinopathies with myeloablative conditioning and rabbit anti-thymocyte globulin.
Bronchitis
Plastic bronchitis and the role of bronchoscopy in the acute chest syndrome of sickle cell disease.
Bronchopulmonary Sequestration
Acute chest syndrome in the postoperative sickle cell patient.
Brugada Syndrome
Atrial fibrillation is associated with sudden cardiac death: a systematic review and meta-analysis.
Brugada syndrome associated with out-of-hospital cardiac arrest: A case report.
Brugada Syndrome: The Role of Risk Stratification in Selecting Patients for Implantable Cardioverter-defibrillator Placement.
Brugada.
Can sudden cardiac death in the young be predicted and prevented? Lessons from autopsy for the emergency physician.
Catheter ablation to prevent sudden cardiac death.
Does the Age of Sudden Cardiac Death in Family Members Matter in Brugada Syndrome?
Electrocardiograms in athletes: interpretation and diagnostic accuracy.
Fragmented QRS and other depolarization abnormalities as a predictor of mortality and sudden cardiac death.
Inherited Arrhythmia Syndrome Predisposing to Sudden Cardiac Death.
Long-term prognosis of patients diagnosed with Brugada syndrome: Results from the FINGER Brugada Syndrome Registry.
Mechanisms of sudden cardiac death.
Monogenec Arrhythmic Syndromes: From Molecular and Genetic Aspects to Bedside.
Outcome of Insertable Cardiac Monitors in Symptomatic Patients with Brugada Syndrome at Low Risk of Sudden Cardiac Death.
Pathogenesis and management of Brugada syndrome in schizophrenia: A scoping review.
Repolarization abnormalities unmasked with exercise in sudden cardiac death survivors with structurally normal hearts.
Risk factors for cardiac events in patients with Brugada syndrome: A PRISMA-compliant meta-analysis and systematic review.
Risk stratification in electrical cardiomyopathies.
Sudden cardiac death in families with premature cardiovascular disease.
Sudden cardiac death in football players: Towards a new pre-participation algorithm.
Sudden cardiac death in Long QT syndrome (LQTS), Brugada syndrome, and catecholaminergic polymorphic ventricular tachycardia (CPVT).
Sudden cardiac death in young competitive athletes due to genetic cardiac abnormalities.
Sudden cause of cardiac death-be aware of me: a case report and short review on brugada syndrome.
The cardiac safety of aripiprazole treatment in patients at high risk for torsade: a systematic review with a meta-analytic approach.
The Postmortem Interpretation of Cardiac Genetic Variants of Unknown Significance in Sudden Death in the Young: A Case Report and Review of the Literature.
TpTe and TpTe/QT: novel markers to predict sudden cardiac death in ESRD?
Ventricular conduction stability test: a method to identify and quantify changes in whole heart activation patterns during physiological stress.
[The ICD as primary prevention. Rare indications]
Bundle-Branch Block
Cardiac arrest recorded on ambulatory electrocardiograms.
Determinants of Sudden Cardiac Death in Adult Patients With Eisenmenger Syndrome.
Mechanism and prediction of sudden cardiac death in arrhythmia patients using electrophysiological studies.
QRS duration predicts sudden cardiac death in hypertensive patients undergoing intensive medical therapy: the LIFE study.
QT prolongation and sudden cardiac death risk in hypertrophic cardiomyopathy.
Sudden cardiac death and malignant arrhythmias: the scope of the problem in adult congenital heart patients.
Sudden cardiac death risk prediction in heart failure with preserved ejection fraction.
Sudden death in patients with chronic bifascicular block.
Carcinogenesis
A hint from zebrafish models of hepatic tumorigenesis: Targeting stearoyl-CoA desaturase.
Adherence and anticarcinogenic effects of Bacillus polyfermenticus SCD in the large intestine.
Chronic exposure to chewing tobacco selects for overexpression of stearoyl-CoA desaturase in normal oral keratinocytes.
Deletion of Stearoyl-CoA Desaturase-1 From the Intestinal Epithelium Promotes Inflammation and Tumorigenesis, Reversed by Dietary Oleate.
Effects of conjugated linoleic acid (CLA) on immune responses, body composition and stearoyl-CoA desaturase.
Immunohistochemical analysis of 11-beta-hydroxysteroid dehydrogenase type 2 and glucocorticoid receptor in subclinical Cushing's disease due to pituitary macroadenoma.
Inhibition of Stearoyl-CoA Desaturase 1 expression in human lung adenocarcinoma cells impairs tumorigenesis.
Loss of stearoyl-CoA desaturase expression is a frequent event in prostate carcinoma.
Positive feedback loop and synergistic effects between hypoxia-inducible factor-2? and stearoyl-CoA desaturase-1 promote tumorigenesis in clear cell renal cell carcinoma.
Shadow cell differentiation in endometrioid carcinomas of the uterus. Its frequent occurrence and beta-catenin expression.
Sickle cell disease induces resistance to cutaneous carcinogenesis.
Stearoyl-CoA desaturase 1 (SCD1) facilitates the growth and anti-ferroptosis of gastric cancer cells and predicts poor prognosis of gastric cancer.
Stearoyl-CoA desaturase activity modulates the activation of epidermal growth factor receptor in human lung cancer cells.
Stearoyl-CoA desaturase and tumorigenesis.
Stearoyl-CoA desaturase plays an important role in proliferation and chemoresistance in human hepatocellular carcinoma.
Stearoyl-CoA Desaturase Promotes Liver Fibrosis and Tumor Development in Mice via a Wnt Positive-Signaling Loop by Stabilization of Low-Density Lipoprotein-Receptor-Related Proteins 5 and 6.
Carcinoma
A Novel Golgi Retention Signal RPWS for Tumor Suppressor UBIAD1.
Bladder carcinoma with shadow cell differentiation: a case report with immunohistochemical analyses.
Chronic exposure to chewing tobacco selects for overexpression of stearoyl-CoA desaturase in normal oral keratinocytes.
Detection of early gene expression changes by differential display in the livers of mice exposed to dichloroacetic acid.
Dynamic high-spatial-resolution MR imaging of invasive ductal carcinoma: influence of histological scirrhous component on MR descriptors.
FADS1 rs174549 Polymorphism May Predict a Favorable Response to Chemoradiotherapy in Oral Cancer Patients.
High Expression of Stearoyl-CoA Desaturase 1 Predicts Poor Prognosis in Patients with Clear-Cell Renal Cell Carcinoma.
Loss of stearoyl-CoA desaturase expression is a frequent event in prostate carcinoma.
Ovarian basaloid carcinoma with shadow cell differentiation.
Positive feedback loop and synergistic effects between hypoxia-inducible factor-2? and stearoyl-CoA desaturase-1 promote tumorigenesis in clear cell renal cell carcinoma.
Shadow Cell Differentiation: A Comparative Analysis of Modes of Cell Death with Apoptosis and Epidermal/Trichilemmal Keratinization.
Stearoyl-CoA desaturase 1 is a novel molecular therapeutic target for clear cell renal cell carcinoma.
The Hypoxic Microenvironment Induces Stearoyl-CoA Desaturase-1 Overexpression and Lipidomic Profile Changes in Clear Cell Renal Cell Carcinoma.
The role of stearoyl-coenzyme A desaturase 1 in clear cell renal cell carcinoma.
Trichothecin inhibits invasion and metastasis of colon carcinoma associating with SCD-1-mediated metabolite alteration.
Y-box binding protein 1 acts as a negative regulator of stearoyl CoA desaturase 1 in clear cell renal cell carcinoma.
Carcinoma in Situ
Endogenous n-3 polyunsaturated fatty acids delay progression of pancreatic ductal adenocarcinoma in Fat-1-p48(Cre/+)-LSL-Kras(G12D/+) mice.
Carcinoma, Basal Cell
Shadow Cell Differentiation: A Comparative Analysis of Modes of Cell Death with Apoptosis and Epidermal/Trichilemmal Keratinization.
Carcinoma, Bronchogenic
Increased levels of vaccenic acid in bronchogenic carcinoma tissue.
Carcinoma, Ductal
Dynamic high-spatial-resolution MR imaging of invasive ductal carcinoma: influence of histological scirrhous component on MR descriptors.
Carcinoma, Hepatocellular
?-Tocotrienol attenuates triglyceride through effect on lipogenic gene expressions in mouse hepatocellular carcinoma Hepa 1-6.
Altered stearoyl-CoA desaturase activities in Morris hepatomas 5123C and 7800.
Analysis of the stearoyl-CoA desaturase system in the Morris hepatoma 7288C and 7288CTC.
Consequences and management of iron overload in sickle cell disease.
delta9 Desaturase activity in normal mouse liver and hepatoma SS1K.
Dietary effects on stearyl coenzyme A desaturase in Morris hepatomas.
DNA ploidy and liver cell dysplasia in liver biopsies from patients with liver cirrhosis.
Downregulation of CPT2 promotes tumorigenesis and chemoresistance to cisplatin in hepatocellular carcinoma.
Effect of bilirubin on triglyceride synthesis in streptozotocin-induced diabetic nephropathy.
PPAR? agonist-induced alterations in ?6-desaturase and stearoyl-CoA desaturase 1: Role of MEK/ERK1/2 pathway.
Role of delta 9 desaturase activity in the maintenance of high levels of monoenoic fatty acids in hepatoma cultured cells.
SCD1 negatively regulates autophagy-induced cell death in human hepatocellular carcinoma through inactivation of the AMPK signaling pathway.
Stearoyl-CoA desaturase 1 coding sequences and antisense RNA affect lipid secretion in transfected chicken LMH hepatoma cells.
Stearoyl-CoA desaturase plays an important role in proliferation and chemoresistance in human hepatocellular carcinoma.
Stearoyl-CoA desaturase regulates sorafenib resistance via modulation of ER stress-induced differentiation.
Targeting stearoyl-CoA desaturase 1 to repress endometrial cancer progression.
Treatment and outcomes of hepatocellular carcinoma in patients with Sickle cell disease: a population-based study in the U.S.
Carcinoma, Medullary
Renal abnormalities in sickle cell disease.
Carcinoma, Renal Cell
High Expression of Stearoyl-CoA Desaturase 1 Predicts Poor Prognosis in Patients with Clear-Cell Renal Cell Carcinoma.
Positive feedback loop and synergistic effects between hypoxia-inducible factor-2? and stearoyl-CoA desaturase-1 promote tumorigenesis in clear cell renal cell carcinoma.
Stearoyl-CoA desaturase 1 is a novel molecular therapeutic target for clear cell renal cell carcinoma.
The Hypoxic Microenvironment Induces Stearoyl-CoA Desaturase-1 Overexpression and Lipidomic Profile Changes in Clear Cell Renal Cell Carcinoma.
The role of stearoyl-coenzyme A desaturase 1 in clear cell renal cell carcinoma.
Y-box binding protein 1 acts as a negative regulator of stearoyl CoA desaturase 1 in clear cell renal cell carcinoma.
Carcinoma, Squamous Cell
Chronic exposure to chewing tobacco selects for overexpression of stearoyl-CoA desaturase in normal oral keratinocytes.
Cardiac Complexes, Premature
Establishment of a predictive model for inpatient sudden cardiac death in a Chinese cardiac department population: a retrospective study.
Cardiac Conduction System Disease
Loss of the transcription factor Meis1 prevents sympathetic neurons target-field innervation and increases susceptibility to sudden cardiac death.
Retrospective analysis of 769 cases of sudden cardiac death from 2006 to 2015: a forensic experience in China.
Cardiac Output, High
Hemodynamic Predictors of Mortality in Adults with Sickle Cell Disease.
Paediatric sickle cell disease: pulmonary hypertension but normal vascular resistance.
Cardiac Tamponade
Retrospective Analysis of Sudden Cardiac Deaths in a 10-Year Autopsy Series in the City of Isparta in Turkey.
Cardio-Renal Syndrome
Arrhythmic complication in cardiorenal syndrome.
Cardiomegaly
Cardiomegaly is a common arrhythmogenic substrate in adult sudden cardiac deaths, and is associated with obesity.
Comparison of risk profiles between survivors and victims of sudden cardiac death from an acute coronary event.
Current perspectives in hypertrophic cardiomyopathy with the focus on patients in the Finnish population: a review.
Exercise tolerance, lung function abnormalities, anemia, and cardiothoracic ratio in sickle cell patients.
Experimental therapies in hypertrophic cardiomyopathy.
Height and risk of sudden cardiac death: the Atherosclerosis Risk in Communities and Cardiovascular Health studies.
Heme Induces IL-6 and Cardiac Hypertrophy Genes Transcripts in Sickle Cell Mice.
Identification of human CDV-1R and mouse Cdv-1R, two novel proteins with putative signal peptides, especially highly expressed in testis and increased with the male sex maturation.
Myocardial cathepsin D is downregulated in sudden cardiac death.
Overexpression of miR-221 in sudden death with cardiac hypertrophy patients.
Pathology of the myocardium and the conduction system in sudden coronary death.
Pulmonary hypertension in sickle cell hemoglobinopathy: a clinicopathologic study of 20 cases.
Retrospective Analysis of Sudden Cardiac Deaths in a 10-Year Autopsy Series in the City of Isparta in Turkey.
Sickle cell disease: at the crossroads of pulmonary hypertension and diastolic heart failure.
Sudden Cardiac Death Among Firefighters ?45 Years of Age in the United States.
Sudden cardiac death during physical exercise: Characteristics of victims and autopsy findings.
Sudden Cardiac Death in the Young: Incidence, Trends, and Risk Factors in a Nationwide Study.
Sudden death in patients with chronic bifascicular block.
Cardiomyopathies
12-lead electrocardiogram as a predictor of sudden cardiac death: from epidemiology to clinical practice.
A comparison of genetic findings in sudden cardiac death victims and cardiac patients: the importance of phenotypic classification.
A patient with severely reduced LV function and electrical storm saved by wearable cardioverter-defibrillator: a case report.
Application of Next Generation Sequencing for personalized medicine for sudden cardiac death.
Application of two novel electrical restitution-based ECG markers of ventricular arrhythmia to patients with nonischemic cardiomyopathy.
Are implantable cardioverter defibrillator shocks a surrogate for sudden cardiac death in patients with nonischemic cardiomyopathy?
Assessing cardiac and liver iron overload in chronically transfused patients with sickle cell disease.
Association between mitochondrial DNA copy number and sudden cardiac death: findings from the Atherosclerosis Risk in Communities study (ARIC).
Asymmetric dimethylarginine predicts appropriate implantable cardioverter-defibrillator intervention in patients with left ventricular dysfunction.
Autosomal-dominant biventricular arrhythmogenic cardiomyopathy in a large family with a novel in-frame DSP nonsense mutation.
Beta-blocker prevents sudden cardiac death in patients with hemodialysis.
Biomarkers in Cardiomyopathies and Prediction of Sudden Cardiac Death.
Body Surface Mapping of T-wave Alternans Depends on the Distribution of Myocardial Scarring.
Cardiac Magnetic Resonance in Primary Prevention of Sudden Cardiac Death.
Cardiac MRI and CT features of inheritable and congenital conditions associated with sudden cardiac death.
Cardiac Screening for High Risk Sudden Cardiac Death in School-Aged Children.
Cardiomegaly is a common arrhythmogenic substrate in adult sudden cardiac deaths, and is associated with obesity.
Cardiomyopathy With Restrictive Physiology in Sickle Cell Disease.
Cardiomyopathy: New SCD risk prediction model.
Cardiovascular genomics and sudden cardiac death in the young.
Carnitine transport by organic cation transporters and systemic carnitine deficiency.
Catheter and Device Management of Inherited Cardiac Conditions.
Cause-of-death analysis in patients with cardiac resynchronization therapy with or without a defibrillator: a systematic review and proportional meta-analysis.
Chronically Transfused Pediatric Sickle Cell Patients are Protected from Cardiac Iron Overload.
Circular RNAs in Sudden Cardiac Death Related Diseases: Novel Biomarker for Clinical and Forensic Diagnosis.
Classic and Novel Biomarkers as Potential Predictors of Ventricular Arrhythmias and Sudden Cardiac Death.
Clinical and Genetic Diagnosis of Nonischemic Sudden Cardiac Death.
Clinical and genetic evaluation after sudden cardiac arrest.
Clinical management and prevention of sudden cardiac death.
Collaborative care for the wearable cardioverter defibrillator patient: Getting the patient and medical team "vested and active".
Combined therapy with PPARalpha agonist and L-carnitine rescues lipotoxic cardiomyopathy due to systemic carnitine deficiency.
Compression entropy contributes to risk stratification in patients with cardiomyopathy.
Cost-effectiveness of in-home automated external defibrillators for individuals at increased risk of sudden cardiac death.
Current Device Therapies for Sudden Cardiac Death Prevention - the ICD, Subcutaneous ICD and Wearable ICD.
Current Indications for Implantable Cardioverter Defibrillators in Non-Ischemic Cardiomyopathies and Channelopathies.
DSP p.(Thr2104Glnfs*12) variant presents variably with early onset severe arrhythmias and left ventricular cardiomyopathy.
Electrocardiograms in athletes: interpretation and diagnostic accuracy.
Electrocardiographic associations with myocardial fibrosis among sudden cardiac death victims.
Electrocardiographic screening in athletes: the time is now for universal screening.
Electrophysiologic Considerations After Sudden Cardiac Arrest.
Epidemiology of sudden cardiac death in patients with heart failure.
Epidemiology of Sudden Cardiac Death: Global and Regional Perspectives.
Excess heme upregulates heme oxygenase 1 and promotes cardiac ferroptosis in mice with sickle cell disease.
Exercise and Inherited Arrhythmias.
Exercise related sudden cardiac death (SCD) in the young - Pre-mortal characterization of a Swedish nationwide cohort, showing a decline in SCD among athletes.
Exercise restrictions for patients with inherited cardiac conditions: Current guidelines, challenges and limitations.
Experts of the Heart Rhythm Section of the Polish Cardiac Society: opinion on the use of wearable cardioverter-defibrillators in Poland.
FIFA Sudden Death Registry (FIFA-SDR): a prospective, observational study of sudden death in worldwide football from 2014 to 2018.
FLNC pathogenic variants in patients with cardiomyopathies: Prevalence and genotype-phenotype correlations.
For Whom the Bell Tolls : Refining Risk Assessment for Sudden Cardiac Death.
Fragmented ECG as a risk marker in cardiovascular diseases.
Fragmented QRS Is a Novel Risk Factor for Ventricular Arrhythmic Events After Receiving Cardiac Resynchronization Therapy in Nonischemic Cardiomyopathy.
Genetic Basis of Ventricular Arrhythmias.
Genetic contributions to the expression of acquired causes of cardiac hypertrophy in non-ischemic sudden cardiac death victims.
Genetic investigations of 100 inherited cardiac disease-related genes in deceased individuals with schizophrenia.
Genetic Variants Associated With Unexplained Sudden Cardiac Death in Adult White and African American Individuals.
IL-18 mediates sickle cell cardiomyopathy and ventricular arrhythmias.
Impact of Chronic Total Coronary Occlusion on Recurrence of Ventricular Arrhythmias in Ischemic Secondary Prevention Implantable Cardioverter-Defibrillator Recipients (VACTO Secondary Study): Insights From Coronary Angiogram and Electrogram Analysis.
Implantable cardioverter defibrillators for the treatment of arrhythmias and cardiac resynchronisation therapy for the treatment of heart failure: systematic review and economic evaluation.
Implantable device therapy.
Incidence and aetiology of sudden cardiac death in young athletes: an international perspective.
Induced ion currents and the endothelin pathway as targets for anti-arrhythmic agents.
Inferolateral early repolarization among non-ischaemic sudden cardiac death victims.
Inverted U-Shaped Relation Between the Risk of Sudden Cardiac Death and Maximal Left Ventricular Wall Thickness in Hypertrophic Cardiomyopathy.
Investigation of the relationship between two novel electrocardiogram-based sudden cardiac death risk markers and autonomic function.
Iron metabolism and iron chelation in sickle cell disease.
Is Exercise Helpful or Harmful in Dealing With Specific Arrhythmia.
Ischemic Heart Disease Related Sudden Cardiac Death in Autopsied Cases: An Egyptian perspective.
Lethal immunoglobulins: Autoantibodies and sudden cardiac death.
Loss of Cadherin-Binding Proteins ?-Catenin and Plakoglobin in the Heart Leads to Gap Junction Remodeling and Arrhythmogenesis.
Massively Parallel Sequencing of Genes Implicated in Heritable Cardiac Disorders: A Strategy for a Small Diagnostic Laboratory.
Mechanism of sudden cardiac death in pigs with viable chronically dysfunctional myocardium and ischemic cardiomyopathy.
Medico-legal perspectives on sudden cardiac death in young athletes.
Metabolic reprogramming of the heart through stearoyl-CoA desaturase.
Molecular autopsy of sudden unexplained deaths reveals genetic predispositions for cardiac diseases among young forensic cases.
Monomorphic Ventricular Arrhythmias in Athletes.
Multimodality imaging predictors of sudden cardiac death.
Narrative review on Morbus Fabry: diagnosis and management of cardiac manifestations.
Next-generation sequencing of 100 candidate genes in young victims of suspected sudden cardiac death with structural abnormalities of the heart.
Non-invasive detection of exercise-induced cardiac conduction abnormalities in sudden cardiac death survivors in the inherited cardiac conditions.
Performance of 2014 NICE defibrillator implantation guidelines in heart failure risk stratification.
Pitfalls in arrhythmogenic left ventricular cardiomyopathy (ALVC). A review of the literature with considerations on a single case of sudden death in a juvenile athlete.
Postmortem imaging of sudden cardiac death.
Pre-participation cardiovascular evaluation in Pacific Island athletes.
Prediction of arrhythmic events with positron emission tomography: PAREPET study design and methods.
Prevalence of arrhythmia-associated gene mutations and risk of sudden cardiac death in the Finnish population.
Prevention of Sudden Cardiac Death in Children and Young Adults.
Prevention of ventricular fibrillation, acute myocardial infarction (myocardial necrosis), heart failure, and mortality by bretylium: is ischemic heart disease primarily adrenergic cardiovascular disease?
Retrospective analysis of 769 cases of sudden cardiac death from 2006 to 2015: a forensic experience in China.
Risk stratification for prevention of sudden cardiac death.
Risk Stratification for Sudden Cardiac Death.
Risk Stratification in Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia Without an Implantable Cardioverter-Defibrillator.
Sacubitril/Valsartan and Sudden Cardiac Death According to Implantable Cardioverter-Defibrillator Use and Heart Failure Cause: A PARADIGM-HF Analysis.
SCD in Patients with Cardiomyopathy: Use of Microvolt T-wave Alternans and Other Noninvasive Tests for Risk Stratification and Prevention of SCD.
Second opinion system for sudden cardiac death cases in forensic practice.
Sex Differences in Electrophysiology, Ventricular Tachyarrhythmia, Cardiac Arrest and Sudden Cardiac Death Following Acute Myocardial Infarction.
Sickle cell disease and pregnancy outcomes: population-based study on 8.8 million births.
Strategies for the prevention and treatment of sudden cardiac death.
Structural pathways and prevention of heart failure and sudden death.
Subcutaneous implantable cardioverter defibrillator in cardiomyopathies and channelopathies.
Sudden arrhythmia death syndrome in young victims: a five-year retrospective review and two-year prospective molecular autopsy study by next-generation sequencing and clinical evaluation of their first-degree relatives.
Sudden cardiac death from structural heart diseases in adults: imaging findings with cardiovascular computed tomography and magnetic resonance.
Sudden cardiac death in athletes: the Lausanne Recommendations.
Sudden cardiac death in China.
Sudden cardiac death in football players: Towards a new pre-participation algorithm.
Sudden cardiac death in nonischemic cardiomyopathy: Refining risk assessment.
Sudden cardiac death in patients with nonischemic cardiomyopathy.
Sudden cardiac death in pediatrics.
Sudden Cardiac Death in the Young: A Strategy for Prevention by Targeted Evaluation.
Sudden cardiac death in the young: Epidemiology and overview.
Sudden cardiac death in young competitive athletes due to genetic cardiac abnormalities.
Sudden cardiac death in young people with apparently normal heart.
Sudden cardiac death rates in an Australian population: a data linkage study.
Sudden Cardiac Death Risk Prediction: The Role of Cardiac Magnetic Resonance Imaging.
Sudden cardiac death.
Sudden cardiac death: focus on the genetics of channelopathies and cardiomyopathies.
Sudden Death Mechanisms in Non-ischemic Cardiomyopathies; Insights gleaned from clinical implantable cardioverter-defibrillator trials.
Sudden death related cardiomyopathies - Arrhythmogenic right ventricular cardiomyopathy, arrhythmogenic cardiomyopathy, and exercise-induced cardiomyopathy.
Sudden Death Risk-Stratification in 2018-2019: The Old and the New.
T wave alternans and ventricular tachyarrhythmia risk stratification: a review.
T-wave variability as a risk stratifier in patients with dilated cardiomyopathy.
Targeted molecular genetic testing in young sudden cardiac death victims from Western Denmark.
The congenital disorder of glycosylation in PGM1 (PGM1-CDG) can cause severe cardiomyopathy and unexpected sudden cardiac death in childhood.
The importance of specialist cardiac histopathological examination in the investigation of young sudden cardiac deaths.
The J wave and fragmented QRS complexes in inferior leads associated with sudden cardiac death in patients with chronic heart failure.
The need for studies to evaluate the reproducibility of the T-wave alternans (TWA), and the rationale for a correction index of the TWA.
The role of nuclear cardiac imaging in risk stratification of sudden cardiac death.
The spectrum of epidemiology underlying sudden cardiac death.
The use of implantable cardioverter defibrillators for the prevention of sudden cardiac death: a review of the evidence and implications.
The yield of postmortem genetic testing in sudden death cases with structural findings at autopsy.
Underdiagnosis of Conditions Associated with Sudden Cardiac Death in Children - Is it the Absence of a Comprehensive Screening Program or a True Low Prevalence?
Update on cardiomyopathies and sudden cardiac death.
Use of genetic testing to identify sudden cardiac death syndromes.
Ventricular tachycardia and sudden cardiac death.
Wearable Cardioverter Defibrillators.
What Is the Arrhythmic Substrate in Viral Myocarditis? Insights from Clinical and Animal Studies.
[A predictive value of ventricular tachycardia detected by long-term electrocardiography for sudden cardiac death]
[Arrhythmogenic dysplasia of right ventricle: pathogenesis, genetic markers, clinical presentation, clinical example]
[Autopsy pathological characteristics in coronary artery disease patients with or without sudden cardiac death].
[Sudden cardiac death : Epidemiology, pathophysiology and risk stratification].
[Sudden cardiac death in diabetes mellitus].
[Sudden cardiac death in women].
[The ICD as primary prevention. Rare indications]
[The retrospective study of sudden cardiac death in 118 cases]
Cardiomyopathy, Alcoholic
[Status of the adrenal medulla in various types of sudden cardiac death]
[Sudden cardiac death: state of the art]
Cardiomyopathy, Dilated
A Novel Risk Stratification Score for Sudden Cardiac Death Prediction in Middle-Aged, Nonischemic Dilated Cardiomyopathy Patients: The ESTIMATED Score.
Application of two novel electrical restitution-based ECG markers of ventricular arrhythmia to patients with nonischemic cardiomyopathy.
Association Between Midwall Late Gadolinium Enhancement and Sudden Cardiac Death in Patients With Dilated Cardiomyopathy and Mild and Moderate Left Ventricular Systolic Dysfunction.
Case report of familial sudden cardiac death caused by a DSG2 p.F531C mutation as genetic background when carrying with heterozygous KCNE5 p.D92E/E93X mutation.
Causes of sudden cardiac death in young athletes and non-athletes: systematic review and meta-analysis: Sudden cardiac death in the young.
Electrocardiograms in athletes: interpretation and diagnostic accuracy.
Future developments in implantable cardioverter defibrillators: the optimal device.
Genetic Variants Are Not Rare in ICD Candidates with Dilated Cardiomyopathy: Time for Next-Generation Sequencing?
Genetics of sudden cardiac death syndromes.
Implantable cardioverter-defibrillator and wait-list outcomes in pediatric patients awaiting heart transplantation.
Inferolateral early repolarization among non-ischaemic sudden cardiac death victims.
Mortality and Sudden Cardiac Death Risk Stratification Using the Noninvasive Combination of Wide QRS Duration and Late Gadolinium Enhancement in Idiopathic Dilated Cardiomyopathy.
Non-sustained ventricular tachycardia as a predictor of sudden cardiac death in patients with left ventricular dysfunction: A meta-analysis.
Pathophysiology and prevention of sudden cardiac death.
Primary systemic carnitine deficiency presenting as recurrent Reye-like syndrome and dilated cardiomyopathy.
Risk stratification for sudden cardiac death in dilated cardiomyopathy using microvolt-level T-wave alternans.
Sudden cardiac death in patients with nonischemic cardiomyopathy.
Sudden Cardiac Death in the Young: A Strategy for Prevention by Targeted Evaluation.
Sudden Cardiac Death in the Young: Incidence, Trends, and Risk Factors in a Nationwide Study.
Sudden cardiac death in young athletes; a literature review and special considerations in Asia.
Sudden Cardiac Death Risk Stratification - An Update.
Sudden cardiac death: A comparative review of humans, dogs and cats.
Sudden death in childhood cardiomyopathy: results from a long-term national population-based study.
Sudden Death Mechanisms in Non-ischemic Cardiomyopathies; Insights gleaned from clinical implantable cardioverter-defibrillator trials.
Sudden death related cardiomyopathies - Arrhythmogenic right ventricular cardiomyopathy, arrhythmogenic cardiomyopathy, and exercise-induced cardiomyopathy.
The J wave and fragmented QRS complexes in inferior leads associated with sudden cardiac death in patients with chronic heart failure.
Towards cardiac MRI based risk stratification in idiopathic dilated cardiomyopathy.
[Another genetic cause of sudden cardiac death].
[Wearable cardioverter-defibrillators: clinical experience and future perspectives].
Cardiomyopathy, Hypertrophic
A Validated Model for Sudden Cardiac Death Risk Prediction in Pediatric Hypertrophic Cardiomyopathy.
A validation study of the 2003 American College of Cardiology/European Society of Cardiology and 2011 American College of Cardiology Foundation/American Heart Association risk stratification and treatment algorithms for sudden cardiac death in patients with hypertrophic cardiomyopathy.
Aborted sudden cardiac death (SCD) in a patient with hypertrophic cardiomyopathy (HCM) with low-risk factors for SCD.
Arrhythmogenic right ventricular cardiomyopathy and sudden cardiac death in young Koreans.
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) in clinical practice.
Can sudden cardiac death in the young be predicted and prevented? Lessons from autopsy for the emergency physician.
Cardiac MRI and CT features of inheritable and congenital conditions associated with sudden cardiac death.
Cardiovascular genomics.
Catheter and Device Management of Inherited Cardiac Conditions.
Causes of nonischemic sudden cardiac death in the current era.
Causes of sudden cardiac death in young athletes and non-athletes: systematic review and meta-analysis: Sudden cardiac death in the young.
Do 'pathologic' cardiac murmurs in adolescents identify structural heart disease? An evaluation of 15 141 active adolescents for conditions that put them at risk of sudden cardiac death.
Electrocardiogram Screening for Disorders That Cause Sudden Cardiac Death in Asymptomatic Children: A Meta-analysis.
Electrocardiogram testing during athletic preparticipation physical examinations.
Electrocardiograms in athletes: interpretation and diagnostic accuracy.
Electrocardiographic Screening for Hypertrophic Cardiomyopathy and Long QT Syndrome: The Drivers of Cost-Effectiveness for the Prevention of Sudden Cardiac Death.
Exercise and Inherited Arrhythmias.
Exercise related sudden cardiac death (SCD) in the young - Pre-mortal characterization of a Swedish nationwide cohort, showing a decline in SCD among athletes.
Exercise restrictions for patients with inherited cardiac conditions: Current guidelines, challenges and limitations.
Genetic screening for hypertrophic cardiomyopathy in large, asymptomatic military cohorts.
Genetics of sudden cardiac death syndromes.
Hereditary Hypertrophic Cardiomyopathy in Children and Young Adults-The Value of Reevaluating and Expanding Gene Panel Analyses.
Holter monitoring in the prognosis of sudden cardiac death.
Hypertrophic Cardiomyopathy in Athletes.
Hypertrophic cardiomyopathy: the importance of arrhythmic events in patients at risk for sudden cardiac death.
Impact of different selection policies on subcutaneous ICD implants and therapies.
Implantable cardioverter-defibrillators in patients with hypertrophic cardiomyopathy -- dilemmas and difficulties.
Incidence and Etiology of Sudden Cardiac Death: New Updates for Athletic Departments.
Is Exercise Helpful or Harmful in Dealing With Specific Arrhythmia.
Left coronary artery anomaly: an often unsuspected cause of sudden death in the military athlete.
Monomorphic Ventricular Arrhythmias in Athletes.
Pathophysiology and prevention of sudden cardiac death.
Prevalence and Spectrum Diseases Predisposing to Sudden Cardiac Death: Are They the Same for Both the Athlete and the Nonathlete?
Prognostic Role of Late Gadolinium Enhancement in Patients With Hypertrophic Cardiomyopathy and Low-to-Intermediate Sudden Cardiac Death Risk Score.
Retrospective Analysis of Sudden Cardiac Deaths in a 10-Year Autopsy Series in the City of Isparta in Turkey.
Risk factors for sudden cardiac death in childhood hypertrophic cardiomyopathy: A systematic review and meta-analysis.
Risk factors for sudden cardiac death to determine high risk patients in specific patient populations that may benefit from a wearable defibrillator.
Sudden arrhythmia death syndrome in young victims: a five-year retrospective review and two-year prospective molecular autopsy study by next-generation sequencing and clinical evaluation of their first-degree relatives.
Sudden Cardiac and Noncardiac Death in Sports: Epidemiology, Causes, Pathogenesis, and Prevention.
Sudden cardiac death in football players: Towards a new pre-participation algorithm.
Sudden cardiac death in infants, children, and adolescents.
Sudden cardiac death in nonischemic cardiomyopathy: Refining risk assessment.
Sudden cardiac death in patients with nonischemic cardiomyopathy.
Sudden Cardiac Death in the Young: A Strategy for Prevention by Targeted Evaluation.
Sudden cardiac death in the young: Epidemiology and overview.
Sudden cardiac death in young athletes; a literature review and special considerations in Asia.
Sudden cardiac death in young competitive athletes due to genetic cardiac abnormalities.
Sudden cardiac death.
Sudden cardiac death: Beware of hasty diagnosis!
Sudden death in childhood cardiomyopathy: results from a long-term national population-based study.
The pathology of hypertrophic cardiomyopathy.
Update on the Diagnostic Pitfalls of Autopsy and Post-Mortem Genetic Testing in Cardiomyopathies.
Update: Causes and symptoms of sudden cardiac death in young athletes.
Validation of the 2020 AHA/ACC Risk Stratification for Sudden Cardiac Death in Chinese Patients With Hypertrophic Cardiomyopathy.
Ventricular arrhythmia following alcohol septal ablation for obstructive hypertrophic cardiomyopathy.
[Antiarrhythmic agents in the prevention of sudden cardiac death]
[Myocardial hypertrophy, arterial hypertension and sudden cardiac death]
[Sudden cardiac death in athletes: is it always not preventable?].
[The ICD as primary prevention. Rare indications]
Cardiomyopathy, Restrictive
Cardiomyopathy With Restrictive Physiology in Sickle Cell Disease.
Implantable cardioverter-defibrillator and wait-list outcomes in pediatric patients awaiting heart transplantation.
Sudden death in childhood cardiomyopathy: results from a long-term national population-based study.
Cardiovascular Abnormalities
Circulating platelet and erythrocyte microparticles in young children and adolescents with sickle cell disease: Relation to cardiovascular complications.
Incidence and aetiology of sudden cardiac death in young athletes: an international perspective.
Left coronary artery anomaly: an often unsuspected cause of sudden death in the military athlete.
Pathological wave dynamics: a postulate for sudden cardiac death in athletes.
Risk of sports: do we need a pre-participation screening for competitive and leisure athletes?
Sudden cardiac death in young athletes: practical challenges and diagnostic dilemmas.
The prevalence and clinical significance of premature ventricular beats in the athlete.
[Premature ventricular beats in young athletes: interpretation and diagnostic pathway].
Cardiovascular Diseases
A common variant at 9p21 is associated with sudden and arrhythmic cardiac death.
A common variant in the ?(2)-adrenergic receptor and risk of sudden cardiac death.
A Novel Golgi Retention Signal RPWS for Tumor Suppressor UBIAD1.
A pilot study of the short-term use of simvastatin in sickle cell disease: effects on markers of vascular dysfunction.
Amino-terminal pro-B-type natriuretic peptide and high-sensitivity C-reactive protein as predictors of sudden cardiac death among women.
Applications of cardiac magnetic resonance imaging in sickle cell disease.
Assessing QT interval prolongation and its associated risks with antipsychotics.
Association between mitochondrial DNA copy number and sudden cardiac death: findings from the Atherosclerosis Risk in Communities study (ARIC).
Association of early repolarization and sudden cardiac death during an acute coronary event.
Association of Waist-Hip Ratio to Sudden Cardiac Death and Severe Coronary Atherosclerosis in Medicolegal Autopsies.
Chronic obstructive pulmonary disease and sudden cardiac death: the Rotterdam study.
CircSLC8A1 and circNFIX can be used as auxiliary diagnostic markers for sudden cardiac death caused by acute ischemic heart disease.
Circular RNAs in Sudden Cardiac Death Related Diseases: Novel Biomarker for Clinical and Forensic Diagnosis.
Clinical determinants and mortality predictability of stearoyl-CoA desaturase-1 activity indices in dialysis patients.
Current controversies in pre-participation cardiovascular screening for young competitive athletes.
Cystatin C and sudden cardiac death risk in the elderly.
Daytime cardiac repolarization in patients with obstructive sleep apnea.
Development and Validation of a Sudden Cardiac Death Prediction Model for the General Population.
Diagnostic yield and financial implications of a nationwide electrocardiographic screening programme to detect cardiac disease in the young.
Diet-gene interactions and PUFA metabolism: a potential contributor to health disparities and human diseases.
Differences in Risk of Sudden Cardiac Death Between Blacks and Whites.
Do insomnia complaints cause hypertension or cardiovascular disease?
Duty-related risk of sudden cardiac death among young US firefighters.
Effects of omega-3 fatty acid for sudden cardiac death prevention in patients with cardiovascular disease: a contemporary meta-analysis of randomized, controlled trials.
Electrocardiographic T Wave Abnormalities and the Risk of Sudden Cardiac Death: The Finnish Perspective.
Exercise Related Sudden Cardiac Death: The Experience of a Tertiary Referral Pathology Centre in the United Kingdom.
Global impairment of cardiac autonomic nervous activity late after repair of tetralogy of Fallot.
Implantable cardioverter defibrillators for prevention of sudden cardiac death.
Markers of Myocardial Stress, Myocardial Injury, and Subclinical Inflammation and the Risk of Sudden Death.
miR-1, miR-499 and miR-208 are sensitive markers to diagnose sudden death due to early acute myocardial infarction.
Moderate alcohol consumption and the risk of sudden cardiac death among US male physicians.
Nationwide burden of sudden cardiac death: A study of 54,028 deaths in Denmark.
Nitric Oxide Synthase 1 Adaptor Protein, an Emerging New Genetic Marker for QT Prolongation and Sudden Cardiac Death.
Novel substituted heteroaromatic compounds as inhibitors of stearoyl-CoA desaturase.
Nutrigenetic associations with cardiovascular disease.
Obstructive Sleep Apnea in Patients with Congenital Long QT Syndrome: Implications for Increased Risk of Sudden Cardiac Death.
Practice viewpoints: AICD, who and when?
Prevalence of Microalbuminuria in Adult Patients with Sickle Cell Disease in Eastern Saudi Arabia.
Prevention of ventricular fibrillation, acute myocardial infarction (myocardial necrosis), heart failure, and mortality by bretylium: is ischemic heart disease primarily adrenergic cardiovascular disease?
Primary prevention of sudden cardiac death.
Relation of atrial and/or ventricular premature complexes on a two-minute rhythm strip to the risk of sudden cardiac death (the Atherosclerosis Risk in Communities [ARIC] study).
Risk and Protective Factors for Sudden Cardiac Death During Leisure Activities in the Mountains: An Update.
Screening young athletes for prevention of sudden cardiac death: Practical recommendations for sports physicians.
Sickle cell disease and H3Africa: enhancing genomic research on cardiovascular diseases in African patients.
Stearoyl-CoA Desaturase: A Vital Checkpoint in the Development and Progression of Obesity.
Sudden cardiac death after manual or automated snow removal.
Sudden Cardiac Death Among Firefighters ?45 Years of Age in the United States.
Sudden Cardiac Death in Hypertensive Patients.
Sudden Cardiac Death in India: A Growing Concern.
Sudden cardiac death in non-dialysis chronic kidney disease patients.
Sudden cardiac death in pediatrics.
Sudden cardiac death in young athletes; a literature review and special considerations in Asia.
Sudden cardiac death rates in an Australian population: a data linkage study.
Sudden Cardiac Death Risk Distribution in the United States Population (from NHANES, 2005 to 2012).
Sudden cardiac death: epidemiology, pathogenesis and management.
Sudden death in athletes: an update.
Sudden death in schizophrenia.
Symptoms and healthcare contact preceding sudden cardiac death in persons aged 1-49 years.
The Atlantic Rift: Guidelines for Athletic Screening-Where Should Canada Stand?
The prevalence and clinical significance of premature ventricular beats in the athlete.
The role of stearoyl-CoA desaturase in body weight regulation.
Unmasking hypertension in children and adolescents with sickle/beta-thalassemia.
Ventricular arrhythmias in the elderly.
Vital exhaustion and sudden cardiac death in the Atherosclerosis Risk in Communities Study.
Vitamin D, parathyroid hormone, and sudden cardiac death: results from the Cardiovascular Health Study.
[Incidence of sudden cardiac death of urban residents in Beijing].
[Sudden cardiac death in athletes: is it always not preventable?].
[Sudden Cardiac Death in Patients With Chronic Obstructive Pulmonary Disease].
Carpal Tunnel Syndrome
[Ultrasonographic evaluation of shoulder joints in hemodialysis patients]
Cat-Scratch Disease
Bartonella henselae Infection in Sickle Cell Disease Mice Is Associated with Hyperalgesia.
Cataract
Canaloplasty with Suprachoroidal Drainage in Patients with Pseudoexfoliation Glaucoma - Four Years Results.
Lens cholesterol biosynthesis inhibition: A common mechanism of cataract formation in laboratory animals by pharmaceutical products.
Catatonia
Catatonic stupor superimposed on hereditary spinocerebellar degeneration resolved with electroconvulsive therapy.
Cell Transformation, Neoplastic
High stearoyl-CoA desaturase protein and activity levels in simian virus 40 transformed-human lung fibroblasts.
Central Nervous System Diseases
Primary and Secondary Stroke Prevention in Children With Sickle Cell Disease.
Central Nervous System Vascular Malformations
Treatment of a cerebral pial arteriovenous fistula in a patient with sickle cell disease-related moyamoya syndrome: case report.
Cerebellar Ataxia
Chronic progressive spinocerebellar syndrome associated with antibodies to human T-lymphotropic virus type I: clinico-virological and magnetic resonance imaging studies.
Distinguishing spinocerebellar ataxia with pure cerebellar manifestation from multiple system atrophy (MSA-C) through saccade profiles.
Prevalence of spinocerebellar degenerations in the Hokuriku district in Japan.
Quantitative evaluation of gait ataxia by accelerometers.
The long loop reflex in spinocerebellar degeneration and motor neuron disease--its changes with TRH therapy.
[A case of spinocerebellar ataxia type 3 (SCA3) associated with isolated ACTH deficiency]
[Cerebello-cerebral functional relationship in spinocerebellar degeneration using positron emission tomography]
[Spinocerebellar degeneration in Japan--the feature from an epidemiological study]
Cerebellar Diseases
Locomotor mal-performance and gait adaptability deficits in sickle cell mice are associated with vascular and white matter abnormalities and oxidative stress in cerebellum.
Cerebral Arterial Diseases
Large-vessel occlusion in sickle cell disease: pathogenesis, clinical consequences, and therapeutic implications.
Cerebral Cortical Thinning
Anxiety correlates with cortical surface area in subjective cognitive decline: APOE ?4 carriers versus APOE ?4 non-carriers.
Different Cortical Thinning Patterns Depending on Their Prognosis in Individuals with Subjective Cognitive Decline.
Reduced cerebrovascular reserve is regionally associated with cortical thickness reductions in children with sickle cell disease.
Regionally Specific Cortical Thinning in Children with Sickle Cell Disease.
Cerebral Hemorrhage
Do chronic pain and comorbidities affect brain function in sickle cell patients? A systematic review of neuroimaging and treatment approaches.
Cerebral Infarction
A Multidisciplinary Health Care Team's Efforts to Improve Educational Attainment in Children With Sickle-Cell Anemia and Cerebral Infarcts.
Abnormal cranial magnetic resonance imaging scans in sickle-cell disease. Neurological correlates and clinical implications.
Automated exchange compared to manual and simple blood transfusion attenuates rise in ferritin level after 1 year of regular blood transfusion therapy in chronically transfused children with sickle cell disease.
Behavioral and emotional problems in children with sickle cell disease and healthy siblings: Multiple informants, multiple measures.
Biomarkers for the central nervous system complications of sickle cell disease: are we there yet?
Blood transfusion therapy is feasible in a clinical trial setting in children with sickle cell disease and silent cerebral infarcts.
Brain-derived neurotrophic factor levels in pediatric sickle cell disease.
Brief Screening Measures Identify Risk for Psychological Difficulties Among Children with Sickle Cell Disease.
Cerebral blood flow measurement in children with sickle cell disease using continuous arterial spin labeling at 3.0-Tesla MRI.
Cerebral Oxygen Metabolic Stress, Microstructural Injury, and Infarction in Adults With Sickle Cell Disease.
Cerebrovascular events in sickle cell-beta thalassemia treated with hydroxyurea: A single center prospective survey in adult Italians.
Children with HbS?0 thalassemia have higher hemoglobin levels and lower incidence rate of acute chest syndrome compared to children with HbSS.
Cognitive functioning in children with sickle cell disease: a meta-analysis.
Cognitive screening examinations for silent cerebral infarcts in sickle cell disease.
Dural Venous Sinus Diameters in Children with Sickle Cell Disease: Correlation with History of Stroke in a Case-Control Study.
Elevation of IgE in children with sickle cell disease is associated with doctor diagnosis of asthma and increased morbidity.
Interventions for preventing silent cerebral infarcts in people with sickle cell disease.
Neurologic complications in children under five years with sickle cell disease.
Neurological soft signs as the stroke risk in sickle cell disease.
Noninvasive central nervous system imaging in sickle cell anemia. A preliminary study comparing transcranial Doppler with magnetic resonance angiography.
Noninvasive optical assessment of resting-state cerebral blood flow in children with sickle cell disease.
Pediatric Neurodevelopmental Delays in Children 0 to 5 Years of Age With Sickle Cell Disease: A Systematic Literature Review.
Plasma glial fibrillary acidic protein levels in children with sickle cell disease.
Practice Patterns of Stroke Screening and Hydroxyurea Use in Children With Sickle Cell Disease: A Survey of Health Care Providers.
Primary and Secondary Stroke Prevention in Children With Sickle Cell Disease.
Proteomic discovery in sickle cell disease: Elevated neurogranin levels in children with sickle cell disease.
Safety of 3 Tesla Magnetic Resonance Imaging in Patients with Sickle Cell Disease.
Sickle cell disease.
Silent brain infarcts are rare in Kuwaiti children with sickle cell disease and high Hb F.
Silent cerebral infarcts occur despite regular blood transfusion therapy after first stroke in children with sickle cell disease.
Spontaneous dissection of the carotid and vertebral arteries: the 10-year UCSD experience.
Thalassemia major and sickle cell disease in adolescents and young adults.
The cognitive and academic impact of sickle cell disease.
The use of extracorporeal membrane oxygenation in pediatric patients with sickle cell disease.
Transition and sickle cell disease.
Cerebral Palsy
Contribution of sickle cell disease to the occurrence of developmental disabilities: a population-based study.
Cerebrovascular Disorders
Association Between Periodic Limb Movements in Sleep and Cerebrovascular Changes in Children With Sickle Cell Disease.
Big strokes in small persons.
Cerebrovascular Disease and Depressive Symptomatology in Individuals With Subjective Cognitive Decline: A Community-Based Study.
Cerebrovascular disease in symptomatic and asymptomatic patients with sickle cell anemia: screening with duplex transcranial Doppler US--correlation with MR imaging and MR angiography.
Electroencephalography hyperventilation and stroke in children with sickle cell disease.
Elevation of tricuspid regurgitant jet velocity, a marker for pulmonary hypertension in children with sickle cell disease.
Hemoglobinopathies and Stroke: Strategies for Prevention and Treatment.
Higher oxygen saturation with hydroxyurea in paediatric sickle cell disease.
Hypoxic adaptation during development: relation to pattern of neurological presentation and cognitive disability.
Is Chlamydia pneumoniae infection associated with stroke in children with sickle cell disease?
Low Rates of Cerebral Infarction after Hematopoietic Stem Cell Transplantation in Patients with Sickle Cell Disease at High Risk for Stroke.
Monitoring retinal pathology and cerebral injury in sickle cell disease using spectral-domain optical coherence tomography in pediatric patients.
Sickle cell disease in pregnancy: maternal complications in a medicaid-enrolled population.
Vascular complications of sickle cell disease.
Chagas Disease
Prevalence of serologic markers of transfusion and sexually transmitted infections and their correlation with clinical features in a large cohort of Brazilian patients with sickle cell disease.
Usefulness of microvolt T-wave alternans for predicting outcome in patients with Chagas disease with implantable cardioverter defibrillators.
CHARGE Syndrome
Utilizing Whole-Exome Sequencing to Characterize the Phenotypic Variability of Sickle Cell Disease.
Cholangitis, Sclerosing
Autoimmune Liver Disease in Patients With Sickle Cell Disease.
Cholecystitis
Abdominal pain in children with sickle cell disease.
Emergency Medicine Management of Sickle Cell Disease Complications: An Evidence-Based Update.
Imaging review of sickle cell disease for the emergency radiologist.
Laparoscopic cholecystectomy for cholelithiasis in children with sickle cell disease.
Protector effect of ?-thalassaemia on cholecystitis and cholecystectomy in sickle cell disease.
Cholecystitis, Acute
Asymptomatic cholelithiasis in children with sickle cell disease: early or delayed cholecystectomy?
Choledocholithiasis
Asymptomatic cholelithiasis in children with sickle cell disease: early or delayed cholecystectomy?
Multiple primary choledocholithiasis in sickle cell disease.
Sequential endoscopic/laparoscopic management of cholelithiasis and choledocholithiasis in children who have sickle cell disease.
Cholelithiasis
Asymptomatic cholelithiasis in children with sickle cell disease: early or delayed cholecystectomy?
Cholelithiasis and biliary tract disease in sickle-cell disease in Nigerians.
Cholelithiasis in children with sickle cell disease.
Early modification of sickle cell disease clinical course by UDP-glucuronosyltransferase 1A1 gene promoter polymorphism.
Elective cholecystectomy reduces morbidity of cholelithiasis in pediatric sickle cell disease.
Laparoscopic cholecystectomy for cholelithiasis in children with sickle cell disease.
Laparoscopic cholecystectomy in adults with sickle cell disease.
Laparoscopic versus open cholecystectomy in children.
Low-impact laparoscopic cholecystectomy is associated with decreased postoperative morbidity in patients with sickle cell disease.
Mini-laparoscopic cholecystectomy in children under 10 years of age with sickle cell disease.
Physiologic effects of pneumoperitoneum in adults with sickle cell disease undergoing laparoscopic cholecystectomy (a case control study).
Polymorphisms in Inflammatory Genes Modulate Clinical Complications in Patients With Sickle Cell Disease.
Prophylactic laparoscopic cholecystectomy in adult sickle cell disease patients with cholelithiasis: A prospective cohort study.
Protector effect of ?-thalassaemia on cholecystitis and cholecystectomy in sickle cell disease.
Sequential endoscopic/laparoscopic management of cholelithiasis and choledocholithiasis in children who have sickle cell disease.
Sickle cell diseases: What can nuclear medicine offer?
Sonographic Diagnosis and Clinical Correlates of Gallbladder Stones in Patients with Sickle Cell Disease in Calabar, Nigeria.
The clinical severity of hemoglobin S/Black ((A) ???)(0) -thalassemia.
The linear effects of alpha-thalassaemia, the UGT1A1 and HMOX1 polymorphisms on cholelithiasis in sickle cell disease.
Treatment of cholelithiasis in children with sickle cell disease.
Cholestasis
Acute and chronic hepatobiliary manifestations of sickle cell disease: A review.
Stearoyl-CoA desaturase deficiency, hypercholesterolaemia, cholestasis and diabetes.
Stearoyl-CoA desaturase deficiency, hypercholesterolemia, cholestasis, and diabetes.
Cholestasis, Intrahepatic
Emergency Medicine Management of Sickle Cell Disease Complications: An Evidence-Based Update.
Liver transplantation in children with sickle-cell disease.
Chylothorax
Use of Pleuroperitoneal Shunt in Chylothorax Related to Central Line Associated Thrombosis in Sickle Cell Disease.
Ciliary Motility Disorders
Lower Airway Nitric Oxide is Increased in Children with Sickle Cell Disease.
Cleft Palate
SLC22A5 Mutations in a Patient With Systemic Primary Carnitine Deficiency and Cleft Palate-Successful Perioperative Management.
Coinfection
A dominant negative form of the transcription factor c-Jun affects genes that have opposing effects on lipid homeostasis in mice.
Colitis
Absence of stearoyl-CoA desaturase-1 does not promote DSS-induced acute colitis.
Metabolomics reveals that hepatic stearoyl-CoA desaturase 1 downregulation exacerbates inflammation and acute colitis.
Colitis, Ulcerative
Clinical and Fecal Microbial Changes With Diet Therapy in Active Inflammatory Bowel Disease.
Evaluating the Comparative Effectiveness of Two Diets in Pediatric Inflammatory Bowel Disease: A Study Protocol for a Series of N-of-1 Trials.
Gangrene of the digits of the right lower limb in a patient with homozygous sickle cell disease and ulcerative colitis.
Specific carbohydrate diet for pediatric inflammatory bowel disease in clinical practice within an academic IBD center.
Colonic Neoplasms
A more physiological approach to lipid metabolism alterations in cancer: CRC-like organoids assessment.
Adherence and anticarcinogenic effects of Bacillus polyfermenticus SCD in the large intestine.
Betulinic Acid Kills Colon Cancer Stem Cells.
ColoLipidGene: signature of lipid metabolism-related genes to predict prognosis in stage-II colon cancer patients.
Lipid metabolism in colon cancer: Role of Liver X Receptor (LXR) and Stearoyl-CoA Desaturase 1 (SCD1).
Stearoyl-CoA Desaturase-1 Enzyme Inhibition by Grape Skin Extracts Affects Membrane Fluidity in Human Colon Cancer Cell Lines.
Targeting a Lipid Desaturation Enzyme, SCD1, Selectively Eliminates Colon Cancer Stem Cells through the Suppression of Wnt and NOTCH Signaling.
Colorectal Neoplasms
Altered Saturated and Monounsaturated Plasma Phospholipid Fatty Acid Profiles in Adult Males with Colon Adenomas.
Feedback activation of AMPK-mediated autophagy acceleration is a key resistance mechanism against SCD1 inhibitor-induced cell growth inhibition.
Is there an added value of faecal calprotectin and haemoglobin in the diagnostic work-up for primary care patients suspected of significant colorectal disease? A cross-sectional diagnostic study.
Loss of mitochondrial aconitase promotes colorectal cancer progression via SCD1-mediated lipid remodeling.
miR-215 Inhibits Colorectal Cancer Cell Migration and Invasion via Targeting Stearoyl-CoA Desaturase.
Stearoyl-CoA desaturase-1 mediated cell apoptosis in colorectal cancer by promoting ceramide synthesis.
Stearoyl-CoA desaturase-1 promotes colorectal cancer metastasis in response to glucose by suppressing PTEN.
Trichothecin inhibits invasion and metastasis of colon carcinoma associating with SCD-1-mediated metabolite alteration.
What influence does intermittent pneumatic compression of the lower limbs intraoperatively have on core hypothermia?
Coma
Comparison of sequential compression devices and foot pumps for prophylaxis of deep venous thrombosis in high-risk trauma patients.
Emergency department risk factors for serious clinical deterioration in a paediatric hospital in Peru.
Commotio Cordis
Blow/trauma to the chest and sudden cardiac death: Commotio cordis and contusio cordis are leading causes.
Sudden cardiac death in the young.
Sudden cardiac death in young athletes; a literature review and special considerations in Asia.
[Sudden cardiac death in athletes: is it always not preventable?].
Communicable Diseases
Degree of Anemia, Indirect Markers of Hemolysis, and Vascular Complications of Sickle Cell Disease in Africa.
Developing a global agenda for sickle cell disease: report of an international symposium and workshop in Cotonou, Republic of Benin.
Life-Threatening Infectious Complications in Sickle Cell Disease: A Concise Narrative Review.
Obstructive sleep apnea syndrome in sickle cell disease.
Preventing Infections in Sickle Cell Disease: The Unfinished Business.
Sickle cell disease related mortality in Brazil, 2000-2018.
Symptoms preceding sudden cardiac death in the young are common but often misinterpreted.
Communication Disorders
A preliminary epidemiologic study of social (pragmatic) communication disorder in the context of developmental language disorder.
A Preliminary Epidemiologic Study of Social (Pragmatic) Communication Disorder Relative to Autism Spectrum Disorder and Developmental Disability Without Social Communication Deficits.
Complex phenotype with social communication disorder caused by mosaic supernumerary ring chromosome 19p.
Neurodevelopmental outcomes in individuals with fetal alcohol spectrum disorder (FASD) with and without exposure to neglect: Clinical cohort data from a national FASD diagnostic clinic.
Confusion
Basal Forebrain Atrophy Is Associated With Allocentric Navigation Deficits in Subjective Cognitive Decline.
Cross-sectional association between physical activity level and subjective cognitive decline among US adults aged ?45 years, 2015.
Gendered racial differences and similarities in subjective cognitive decline and life satisfaction: results from a population-based sample.
Histologic and Ultrastructural Findings in Dogs With Chronic Respiratory Disease Suspected of Ciliary Dyskinesia.
Racial and ethnic differences in post-stroke subjective cognitive decline exist.
Unmet needs for assistance related to subjective cognitive decline among community-dwelling middle-aged and older adults in the US: prevalence and impact on health-related quality of life.
Congenital Abnormalities
A call for policy action in sub-Saharan Africa to rethink diagnostics for pregnancy affected by sickle cell disease: differential views of medical doctors, parents and adult patients predict value conflicts in Cameroon.
Challenge for management without tracheostomy tube after laryngo-tracheal separation in children with neurological disorders.
Defining an Algorithm of Treatment for Severe Cervical Deformity Using Surgeon Survey and Treatment Patterns.
Incidence and Classification of Chest Wall Deformities in Breast Augmentation Patients.
Incidence and clinical characteristics of sudden cardiac death in adult congenital heart disease.
Induced ion currents and the endothelin pathway as targets for anti-arrhythmic agents.
Morphometry of the thoracolumbar vertebrae in sickle cell disease.
Multiple bone and joint diseases in a nigerian sickle cell anaemia: a case report.
Parents' assessment of risk in sickle cell disease treatment with hydroxyurea.
Preliminary Results of Multiple Epiphyseal Drilling and Autologous Bone Marrow Implantation for Osteonecrosis of the Femoral Head Secondary to Sickle Cell Disease in Children.
Preparticipation athletic screening for genetic heart disease.
Prevention of Sudden Cardiac Death in Adults With Congenital Heart Disease: Do the Guidelines Fall Short?
Rates of New Neurological Deficit Associated with Spine Surgery Based on 108,419 Procedures: A Report of the Scoliosis Research Society Morbidity and Mortality Committee.
Spondylocostal dysostosis associated with right-sided polythelia, right-sided rib deformity and meningocoele: Case report with review of literature.
Spondylocostal dysostosis with tetralogy of Fallot and herniation of the spleen through the diaphragm.
Sudden cardiac death in adults with congenital heart disease: does QRS-complex fragmentation discriminate in structurally abnormal hearts?
Vertical expandable prosthetic titanium rib as treatment of thoracic insufficiency syndrome in spondylocostal dysplasia.
Congenital Hypothyroidism
Infants with Congenital Disorders Identified Through Newborn Screening - United States, 2015-2017.
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
The congenital disorder of glycosylation in PGM1 (PGM1-CDG) can cause severe cardiomyopathy and unexpected sudden cardiac death in childhood.
Corneal Dystrophies, Hereditary
Schnyder Corneal Dystrophy-Associated UBIAD1 is Defective in MK-4 Synthesis and Resists Autophagy-Mediated Degradation.
The Oskar Fehr Lecture.
Coronary Artery Disease
A case-control study between the gene polymorphisms of polyunsaturated fatty acids metabolic rate-limiting enzymes and coronary artery disease in a Chinese Han population.
A common variant at 9p21 is associated with sudden and arrhythmic cardiac death.
A guide to device selection: cardiac resynchronization therapy alone or in combination with an implantable cardioverter defibrillator.
A histopathological analysis of the epidemiology of coronary atherosclerosis: an autopsy study.
An association between right ventricular dysfunction and sudden cardiac death.
Are women worldwide under-treated with regard to cardiac resynchronization and sudden death prevention?
Association of Silent Myocardial Infarction and Sudden Cardiac Death.
Association of the FADS gene cluster with coronary artery disease and plasma lipid concentrations in the northern Chinese Han population.
Atrial fibrillation and its association with sudden cardiac death.
Atrial fibrillation is associated with sudden cardiac death: a systematic review and meta-analysis.
Beta-blocker prevents sudden cardiac death in patients with hemodialysis.
Biomarkers as predictors of sudden cardiac death in coronary artery disease patients with preserved left ventricular function (ARTEMIS study).
Cardiac arrhythmias and conduction disturbances in autoimmune rheumatic diseases.
Cardiac MRI and CT features of inheritable and congenital conditions associated with sudden cardiac death.
Chronic Obstructive Pulmonary Disease and Risk of Sudden Cardiac Death.
Circular RNAs in Sudden Cardiac Death Related Diseases: Novel Biomarker for Clinical and Forensic Diagnosis.
Classic and Novel Biomarkers as Potential Predictors of Ventricular Arrhythmias and Sudden Cardiac Death.
Clinical and genetic evaluation after sudden cardiac arrest.
Clinical characteristics of unexplained sudden cardiac death in Korea.
Common beta-adrenergic receptor polymorphisms are not associated with risk of sudden cardiac death in patients with coronary artery disease.
Comparison of risk profiles between survivors and victims of sudden cardiac death from an acute coronary event.
Coronary artery disease in athletes: An adverse effect of intense exercise?
Coronary atherosclerosis in unheralded sudden coronary death under age 50: histo-pathologic comparison with 'healthy' subjects dying out of hospital.
Cumulative effects of common genetic variants on risk of sudden cardiac death.
Current smoking, smoking cessation, and the risk of sudden cardiac death in patients with coronary artery disease.
Decreased mRNA levels of cardiac Cx43 and ZO1 in sudden cardiac death related to coronary atherosclerosis: a pilot study.
Determinants of prolonged QT interval and their contribution to sudden death risk in coronary artery disease: the Oregon Sudden Unexpected Death Study.
Dialysis modality-related disparities in sudden cardiac death: hemodialysis versus peritoneal dialysis.
Dietary n-3 polyunsaturated fatty acid intakes modify the effect of genetic variation in fatty acid desaturase 1 on coronary artery disease.
Do athletes play by different rules? Obstructive coronary artery disease in asymptomatic competitive Masters athletes: a case series.
Effect of Sex and Underlying Disease on the Genetic Association of QT Interval and Sudden Cardiac Death.
Electrocardiographic Markers and the Left Ventricular Ejection Fraction have Cumulative Effects on Risk of Sudden Cardiac Death.
Epidemiology and genetics of ventricular fibrillation during acute myocardial infarction.
Epidemiology and stratification of risk for sudden cardiac death.
Expression of androgen receptor in coronary artery in the cases of sudden coronary death.
Expressions of SOCS-1 and SOCS-3 in the myocardium of patients with sudden cardiac death.
Feasibility of entirely subcutaneous ICD™ systems in patients with coronary artery disease.
Fragmented ECG as a risk marker in cardiovascular diseases.
Genetic predisposition to sudden cardiac death.
Genetics of sudden cardiac death.
Heart rate variability (HRV) in kidney failure: measurement and consequences of reduced HRV.
Hypertension, left ventricular hypertrophy, and sudden death.
Increase in sudden death from coronary artery disease in young adults.
Increased Left Ventricular Mass and Decreased LV Systolic Function Have Independent Pathways to Ventricular Arrhythmogenesis in Coronary Artery Disease.
Interleukin 18 gene promoter polymorphism: a link between hypertension and pre-hospital sudden cardiac death: the Helsinki Sudden Death Study.
Is hypertensive left ventricular hypertrophy a cause of sustained ventricular arrhythmias in humans?
Ischemic Heart Disease Related Sudden Cardiac Death in Autopsied Cases: An Egyptian perspective.
Lambda-like ST segment elevation in acute myocardial infarction - a new risk marker for ventricular fibrillation? Three case reports.
Long-term follow-up after atrioventricular nodal ablation and pacing: low incidence of sudden cardiac death.
Management of arrhythmias in ischemic heart disease. The role of beta blockers.
Marathon related cardiac arrest risk differences in men and women.
Mechanisms of sudden cardiac death.
miR-3113-5p, miR-223-3p, miR-133a-3p, and miR-499a-5p are sensitive biomarkers to diagnose sudden cardiac death.
Molecular autopsy in victims of inherited arrhythmias.
Molecular autopsy of sudden unexplained deaths reveals genetic predispositions for cardiac diseases among young forensic cases.
Monogenec Arrhythmic Syndromes: From Molecular and Genetic Aspects to Bedside.
Myocardial infarction or acute coronary syndrome with non-obstructive coronary arteries and sudden cardiac death: a missing connection.
Myocardial ischemia and right ventricular dysfunction in adult patients with sickle cell disease.
n-3 fatty acids and the risk of sudden cardiac death.
Nationwide (Denmark) Study of Symptoms Preceding Sudden Death due to Arrhythmogenic Right Ventricular Cardiomyopathy.
Nitric Oxide Synthase 1 Adaptor Protein, an Emerging New Genetic Marker for QT Prolongation and Sudden Cardiac Death.
Novel approaches for the treatment of ventricular tachycardia.
Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease.
Opportunities for sudden death prevention: directions for new clinical and basic research.
Pathology of the myocardium and the conduction system in sudden coronary death.
Pathophysiology and prevention of sudden cardiac death.
Pathophysiology, risk stratification, and management of sudden cardiac death in coronary artery disease.
Physical Activity and the Risk for Sudden Cardiac Death in Patients With Coronary Artery Disease.
Platelet glycoprotein Ibalpha HPA-2 Met/VNTR B haplotype as a genetic predictor of myocardial infarction and sudden cardiac death.
Polymorphisms in FADS1 and FADS2 alter plasma fatty acids and desaturase levels in type 2 diabetic patients with coronary artery disease.
Postmortem mRNA expression patterns in left ventricular myocardial tissues and their implications for forensic diagnosis of sudden cardiac death.
Predictors of cardiac arrhythmic events in non coronary artery disease patients.
Prevention of Sudden Cardiac Death in Children and Young Adults.
Prevention of sudden cardiac death: lessons from recent controlled trials.
Reduced left ventricular ejection fraction and sudden cardiac death in patients undergoing revascularization: Time to remember the other players of the game.
Remote ischemic preconditioning differentially attenuates post-ischemic cardiac arrhythmia in streptozotocin-induced diabetic versus nondiabetic rats.
Risk factors and prognostic role of an electrical storm in patients after myocardial infarction with an implanted ICD for secondary prevention.
Risk stratification and management of sudden cardiac death: a new paradigm.
Risk Stratification for Sudden Cardiac Death.
Role of risk stratification and genetics in sudden cardiac death.
SCD rs41290540 single-nucleotide polymorphism modifies miR-498 binding and is associated with a decreased risk of coronary artery disease.
Second opinion system for sudden cardiac death cases in forensic practice.
Sports-related sudden cardiac deaths in the young population of Switzerland.
Strategies for the prevention and treatment of sudden cardiac death.
Sudden Cardiac and Noncardiac Death in Sports: Epidemiology, Causes, Pathogenesis, and Prevention.
Sudden Cardiac Death (SCD) - risk stratification and prediction with molecular biomarkers.
Sudden cardiac death and chronic kidney disease: From pathophysiology to treatment strategies.
Sudden cardiac death and coronary disease in the young: A nationwide cohort study in Denmark.
Sudden cardiac death during physical exercise: Characteristics of victims and autopsy findings.
Sudden cardiac death following liver transplantation: Incidence, trends and risk predictors.
Sudden cardiac death from structural heart diseases in adults: imaging findings with cardiovascular computed tomography and magnetic resonance.
Sudden cardiac death in athletes.
Sudden Cardiac Death in Brazil: A Community-Based Autopsy Series (2006-2010).
Sudden cardiac death in cardiac transplant recipients.
Sudden cardiac death in China.
Sudden cardiac death in football.
Sudden cardiac death in hemodialysis patients: an in-depth review.
Sudden Cardiac Death in India: A Growing Concern.
Sudden cardiac death in patients with chronic coronary heart disease.
Sudden cardiac death in patients with stable coronary artery disease and preserved left ventricular systolic function.
Sudden cardiac death in the young.
Sudden cardiac death in the young: how can disease recognition and prevention in family members be improved?
Sudden Cardiac Death in the Young: Incidence, Trends, and Risk Factors in a Nationwide Study.
Sudden cardiac death in the young: the molecular autopsy and a practical approach to surviving relatives.
Sudden Cardiac Death in Women With Suspected Ischemic Heart Disease, Preserved Ejection Fraction, and No Obstructive Coronary Artery Disease: A Report From the Women's Ischemia Syndrome Evaluation Study.
Sudden cardiac death in women.
Sudden cardiac death in young people with apparently normal heart.
Sudden Cardiac Death not Related to Coronary Atherosclerosis.
Sudden Cardiac Death Risk Prediction: The Role of Cardiac Magnetic Resonance Imaging.
Sudden Cardiac Death: A Review Focused on Cardiovascular Imaging.
Sudden cardiac death: epidemiology and temporal trends.
Sudden cardiac death: epidemiology, causes, and mechanisms.
Sudden cardiac death: epidemiology, circadian variation, and triggers.
Sudden death in cardiac sarcoidosis: an analysis of nationwide clinical and cause-of-death registries.
SVAD: A genetic database curates non-ischemic sudden cardiac death-associated variants.
T-wave reversal in the augmented unipolar right arm electrocardiographic lead is associated with increased risk of sudden death.
Temporal Trends in the Clinical and Pathological Characteristics of Victims of Sudden Cardiac Death in the Absence of Previously Identified Heart Disease.
The 12-lead electrocardiogram and risk of sudden death: current utility and future prospects.
The automatic implantable defibrillator is the most realistic and cost-effective way of preventing sudden cardiac death.
The effect of aldosterone antagonists for ventricular arrhythmia: a meta-analysis.
The effect of coronary bypass graft surgery for the prevention of sudden cardiac death: recurrent episodes after ICD implantation and review of literature.
The relationship between left ventricular scar and ventricular repolarization in patients with coronary artery disease: insights from late gadolinium enhancement magnetic resonance imaging.
Update on cardiomyopathies and sudden cardiac death.
Use of genetic testing to identify sudden cardiac death syndromes.
Usefulness of Single Nucleotide Polymorphisms as Predictors of Sudden Cardiac Death.
Usefulness of the Duke Sudden Cardiac Death risk score for predicting sudden cardiac death in patients with angiographic (>75% narrowing) coronary artery disease.
Validity of plasma remnant lipoproteins as surrogate markers of antemortem level in cases of sudden coronary death.
Ventricular Arrhythmias Among Implantable Cardioverter-Defibrillator Recipients for Primary Prevention: Impact of Chronic Total Coronary Occlusion (VACTO Primary Study).
[Antiarrhythmic agents in the prevention of sudden cardiac death]
[Autopsy pathological characteristics in coronary artery disease patients with or without sudden cardiac death].
[Expression of monocyte chemotactic protein-1 and its receptor in sudden coronary death].
[Monocyte chemotactic protein-1 expression in coronary atherosclerosis plaque of sudden coronary death patients]
[Sudden cardiac death: epidemiology and modern therapy]
[Sudden cardiac death: toward the identification of susceptibity genes]
[The retrospective study of sudden cardiac death in 118 cases]
Coronary Disease
12-lead electrocardiogram as a predictor of sudden cardiac death: from epidemiology to clinical practice.
A pathological study of sudden coronary death in China: report of 89 autopsy cases.
Amino-terminal pro-B-type natriuretic peptide and high-sensitivity C-reactive protein as predictors of sudden cardiac death among women.
An epidemiologic and histopathological study of sudden cardiac death in Osaka Medical Examiner's Office.
Association of Dietary Magnesium Intake with Fatal Coronary Heart Disease and Sudden Cardiac Death.
Cardiorespiratory fitness is related to the risk of sudden cardiac death: a population-based follow-up study.
Continued high incidence of coronary artery disease at autopsy in Olmsted County, Minnesota, 1950 to 1979.
Echocardiographic Predictors of Sudden Cardiac Death: The Atherosclerosis Risk in Communities Study and Cardiovascular Health Study.
Electrocardiogram as a screening tool in the general population: A strategic review.
Electrophysiological and therapeutic implications of cardiac arrhythmias in hypertension.
Epidemiology and stratification of risk for sudden cardiac death.
Epidemiology of Sudden Cardiac Death: Global and Regional Perspectives.
Expression of androgen receptor in coronary artery in the cases of sudden coronary death.
Expressions of SOCS-1 and SOCS-3 in the myocardium of patients with sudden cardiac death.
Fatty acid desaturase 1 polymorphisms are associated with coronary heart disease in a Chinese population.
Future developments in implantable cardioverter defibrillators: the optimal device.
Genetic variations in nitric oxide synthase 1 adaptor protein are associated with sudden cardiac death in US white community-based populations.
Genomics in sudden cardiac death.
Genomics, heart failure and sudden cardiac death.
Global Electric Heterogeneity Risk Score for Prediction of Sudden Cardiac Death in the General Population: The Atherosclerosis Risk in Communities (ARIC) and Cardiovascular Health (CHS) Studies.
Height and risk of sudden cardiac death: the Atherosclerosis Risk in Communities and Cardiovascular Health studies.
Histopathology of the conduction system in sudden death from coronary heart disease.
Holter monitoring in the prognosis of sudden cardiac death.
Impaired Fasting Plasma Glucose and Type 2 Diabetes Are Related to the Risk of Out-of-Hospital Sudden Cardiac Death and All-Cause Mortality.
Implantable device therapy.
Incidence and Predictors of Sudden Cardiac Death After a Major Non-Fatal Cardiovascular Event.
Interleukin 18 gene promoter polymorphism: a link between hypertension and pre-hospital sudden cardiac death: the Helsinki Sudden Death Study.
Is High Serum LDL/HDL Cholesterol Ratio an Emerging Risk Factor for Sudden Cardiac Death? Findings from the KIHD Study.
Lifetime Risk for Sudden Cardiac Death in the Community.
Long- and short-term risk of sudden coronary death.
Long-term prognosis associated with early repolarisation pattern in Chinese population with atherosclerotic risk factors.
Mediterranean Diet Score, Dietary Patterns, and Risk of Sudden Cardiac Death in the REGARDS Study.
Omega-3 Supplementation and Heart Disease: A Population-Based Diet by Gene Analysis of Clinical Trial Outcomes.
Out of hospital sudden cardiac death in Italy: a population-based case-control study.
Pathology of the myocardium and the conduction system in sudden coronary death.
Prediction and prevention of sudden cardiac death.
Predictors of sudden cardiac death in atrial fibrillation: The Atherosclerosis Risk in Communities (ARIC) study.
Prolonged QRS duration on the resting ECG is associated with sudden death risk in coronary disease, independent of prolonged ventricular repolarization.
Prospective study of sudden cardiac death among women in the United States.
Regression of electrocardiographic left ventricular hypertrophy during antihypertensive therapy and reduction in sudden cardiac death: the LIFE Study.
Relation of atrial and/or ventricular premature complexes on a two-minute rhythm strip to the risk of sudden cardiac death (the Atherosclerosis Risk in Communities [ARIC] study).
Relation of systemic blood pressure to sudden cardiac death.
Risk of sudden coronary death based on genetic background in Chinese Han population.
Roadway proximity and risk of sudden cardiac death in women.
Significances of viable synergistic autophagy-associated cathepsin B and cathepsin D (CTSB/CTSD) as potential biomarkers for sudden cardiac death.
State-specific mortality from sudden cardiac death--United States, 1999.
Structural pathways and prevention of heart failure and sudden death.
Sudden Cardiac Death Among Firefighters ?45 Years of Age in the United States.
Sudden cardiac death in patients with nonischemic cardiomyopathy.
Sudden cardiac death in the Kazakh and Han peoples of Xinjiang, China: A comparative cross-sectional study.
Sudden Cardiac Death in Young Adult.
Sudden cardiac death: epidemiology, pathogenesis and management.
Sudden cardiac death: from molecular biology and cellular electrophysiology to therapy.
Sudden coronary death in middle age and characteristics of its victims in Finland. A prospective population study.
Sudden death in patients with chronic bifascicular block.
Sudden out-of-hospital coronary death in patients with no previous cardiac history. An analysis of 221 patients studied at autopsy.
The -1C to T polymorphism in the annexin A5 gene is not associated with the risk of acute myocardial infarction or sudden cardiac death in middle-aged Finnish males.
The relationship between high resting heart rate and ventricular arrhythmogenesis in patients referred to ambulatory 24 h electrocardiographic recording.
The spectrum of epidemiology underlying sudden cardiac death.
Thyroid-stimulating hormone and risk of sudden cardiac death, total mortality and cardiovascular morbidity.
[Alcoholic cardiomyopathy - a risk factor in sudden death]
[Arrhythmogenic dysplasia of right ventricle: pathogenesis, genetic markers, clinical presentation, clinical example]
[Autopsies are essential for a better knowledge and prevention of sudden cardiac death].
[Primary prevention of sudden cardiac death implanted cardioverter defibrillator (ICD) versus antiarrhythmic drugs]
[Psychological and psychosocial factors in sudden cardiac death]
Coronary Occlusion
Pathophysiology of coronary artery disease leading to acute coronary syndromes.
Post-mortem CMR in a model of sudden death due to myocardial ischemia: validation with connexin-43.
Coronary Stenosis
Coronary stenosis as a modifier of the effect of cold spells on the risk of sudden cardiac death: a case-crossover study in Finland.
Forensic Pathological Study of 1656 Cases of Sudden Cardiac Death in Southern China.
Impact of Percutaneous Revascularization on Exercise Hemodynamics in Patients With Stable Coronary Disease.
Optical Coherence Tomography for the Diagnosis of Exercise-Related Acute Cardiovascular Events and Inconclusive Coronary Angiography.
Platelet glycoprotein Ibalpha HPA-2 Met/VNTR B haplotype as a genetic predictor of myocardial infarction and sudden cardiac death.
Remnant lipoproteins from patients with sudden cardiac death enhance coronary vasospastic activity through upregulation of Rho-kinase.
[Alcoholic cardiomyopathy - a risk factor in sudden death]
[Autopsy pathological characteristics in coronary artery disease patients with or without sudden cardiac death].
Coronary Thrombosis
Glycoprotein IIIa Pl(A1/A2) polymorphism and sudden cardiac death.
Pathology of the myocardium and the conduction system in sudden coronary death.
Platelet glycoprotein Ibalpha HPA-2 Met/VNTR B haplotype as a genetic predictor of myocardial infarction and sudden cardiac death.
Sudden out-of-hospital coronary death in patients with no previous cardiac history. An analysis of 221 patients studied at autopsy.
Coronary Vasospasm
Masked inherited primary arrhythmia syndromes in sudden cardiac death patients accompanied by coronary vasospasm.
Multi-vessel intractable coronary spasm development in a patient with aborted sudden cardiac death: a case study with intravascular ultrasound findings.
Remnant lipoproteins from patients with sudden cardiac death enhance coronary vasospastic activity through upregulation of Rho-kinase.
Cough
Atypical presentation of acute post-infectious glomerulonephritis in patients with sickle cell disease: report of two cases.
COVID-19 Presentation in Patients with Sickle Cell Disease: A Case Series.
Utility of Point-of-Care Lung Ultrasonography for Evaluating Acute Chest Syndrome in Young Patients With Sickle Cell Disease.
Which Febrile Children with Sickle Cell Disease Need a Chest X-Ray?
COVID-19
A possible pathogenic role of Syndecan-1 in the pathogenesis of coronavirus disease 2019 (COVID-19).
Anxiety level and clinical course of patients with sickle cell disease during the COVID-19 outbreak.
Challenges in the Management of Sickle Cell Disease During SARS-CoV-2 Pandemic.
Changes in Care Delivery for Children With Sickle Cell Anemia During the COVID-19 Pandemic.
Clinical predictors of poor outcomes in patients with sickle cell disease and COVID-19 infection.
Comorbidities are risk factors for hospitalization and serious COVID-19 illness in children and adults with sickle cell disease.
Comparison of the clinical course of COVID-19 infection in sickle cell disease patients with healthcare professionals.
COVID-19 and Sickle Cell Disease in Bahrain.
COVID-19 and the pulmonary complications of sickle cell disease.
COVID-19 in individuals with sickle cell disease/trait compared with other Black individuals.
COVID-19 in Saudi Patients With Sickle Cell Disease: A Retrospective Multi-Center Study.
COVID-19 Presentation in Patients with Sickle Cell Disease: A Case Series.
COVID-19: an unprecedented pandemia with a potential arrhythmic undertone.
Hemoglobinopathy and pediatrics in the time of COVID-19.
Identification of Causal Genes of COVID-19 Using the SMR Method.
Implications of COVID-19 infections in sickle cell disease.
Is sickle cell disease a risk factor for severe COVID-19 outcomes in hospitalized patients? A multicenter national retrospective cohort study.
Potential Implications of a Type 1 Interferon Gene Signature on COVID-19 Severity and Chronic Inflammation in Sickle Cell Disease.
Preliminary Data on COVID-19 in Patients with Hemoglobinopathies: A Multicentre ICET-A Study.
Severe COVID-19 with acute respiratory distress syndrome (ARDS) in a sickle cell disease adult patient: case report.
Severe hemolysis and vaso-occlusive crisis due to COVID-19 infection in a sickle cell disease patient improved after red blood cell exchange.
Sickle cell disease and COVID-19: Susceptibility and severity.
Spinal cord dysfunction after COVID-19 infection.
Stroke and presence of patent foramen ovale in sickle cell disease.
The Effects of COVID-19 and Quarantine Measures on the Lifestyles and Mental Health of People Over 60 at Increased Risk of Dementia.
Treatment of Cytokine Storm in COVID-19 Patients with Immunomodulatory Therapy.
Treatment of Cytokine Storm in COVID-19 Patients With Immunomodulatory Therapy.
Craniocerebral Trauma
Comparison of sequential compression devices and foot pumps for prophylaxis of deep venous thrombosis in high-risk trauma patients.
Temporal bone fracture causing superior semicircular canal dehiscence.
Craniofacial Abnormalities
Craniofacial morphology in patients with sickle cell disease: a cephalometric analysis.
Crohn Disease
Clinical and Fecal Microbial Changes With Diet Therapy in Active Inflammatory Bowel Disease.
Evaluating the Comparative Effectiveness of Two Diets in Pediatric Inflammatory Bowel Disease: A Study Protocol for a Series of N-of-1 Trials.
Lack of Mucosal Healing From Modified Specific Carbohydrate Diet in Pediatric Patients With Crohn Disease.
Specific carbohydrate diet for pediatric inflammatory bowel disease in clinical practice within an academic IBD center.
cystathionine beta-synthase deficiency
Cystathionine ?-synthase-deficient mice thrive on a low-methionine diet.
Cystic Fibrosis
Burden of influenza-related hospitalizations among children with sickle cell disease.
Health related quality of life in sickle cell patients: the PiSCES project.
Infants with Congenital Disorders Identified Through Newborn Screening - United States, 2015-2017.
Long-term central venous access in patients with sickle cell disease. Incidence of thrombotic and infectious complications.
Managing the acutely ill adult with sickle cell disease.
The Effect of Structural Violence on Patients with Sickle Cell Disease.
Cystinosis
Differential diagnosis of Schnyder corneal dystrophy.
Cysts
Increased prevalence of renal cysts in patients with sickle cell disease.
Laparoscopic splenic procedures in children: experience in 231 children.
Squamous Cell Differentiation in Metastatic Papillary Thyroid Carcinoma: Metaplastic Reversion or Progression?
cytochrome-b5 reductase deficiency
Smooth muscle cytochrome b5 reductase 3 deficiency accelerates pulmonary hypertension development in sickle cell mice.
Deafness
Deafness and sickle cell disease: three case reports and review of the literature.
Death, Sudden, Cardiac
A common variant at 9p21 is associated with sudden and arrhythmic cardiac death.
A Novel COX10 Deletion Polymorphism as a Susceptibility Factor for Sudden Cardiac Death Risk in Chinese Populations.
A Novel Risk Stratification Score for Sudden Cardiac Death Prediction in Middle-Aged, Nonischemic Dilated Cardiomyopathy Patients: The ESTIMATED Score.
A Validated Model for Sudden Cardiac Death Risk Prediction in Pediatric Hypertrophic Cardiomyopathy.
A validation study of the 2003 American College of Cardiology/European Society of Cardiology and 2011 American College of Cardiology Foundation/American Heart Association risk stratification and treatment algorithms for sudden cardiac death in patients with hypertrophic cardiomyopathy.
Aborted sudden cardiac death (SCD) in a patient with hypertrophic cardiomyopathy (HCM) with low-risk factors for SCD.
Activity immediately before the onset of non-fatal myocardial infarction and sudden cardiac death.
Adherence to a low-risk, healthy lifestyle and risk of sudden cardiac death among women.
Alternative Research Funding to Improve Clinical Outcomes: The Model of Prediction and Prevention of Sudden Cardiac Death.
Analysis of SNP (single nucleotide polymorphism) multiplex markers related to sudden cardiac death in Brazilian families.
Arrhythmia in Cardiac Sarcoidosis.
Association Between Malignant Mitral Valve Prolapse and Sudden Cardiac Death: A Review.
Association of QT-Prolonging Medications With Risk of Autopsy-Defined Causes of Sudden Death.
Associations between common ion channel single nucleotide polymorphisms and sudden cardiac death in adults: A MOOSE-compliant meta-analysis.
Baseline and long-term fibrinogen levels and risk of sudden cardiac death: A new prospective study and meta-analysis.
Blood alcohol levels in Finnish victims of non-ischaemic sudden cardiac death.
Body Mass Index as a Predictor of Sudden Cardiac Death and Usefulness of the Electrocardiogram for Risk Stratification.
Canadian Cardiovascular Society/Canadian Heart Rhythm Society Joint Position Statement on the Cardiovascular Screening of Competitive Athletes.
Cardiac arrest recorded on ambulatory electrocardiograms.
Cardiac magnetic resonance characteristics in young survivors of aborted sudden cardiac death.
Cardiac Magnetic Resonance Imaging Features in Hypertrophic Cardiomyopathy Diagnosed at <21 Years of Age.
Cardiorespiratory Fitness and Risk of Sudden Cardiac Death in Men and Women in the United States: A Prospective Evaluation From the Aerobics Center Longitudinal Study.
Cardiovascular Disease: Cardioverter-Defibrillators and Left Ventricular Assist Devices.
Catecholaminergic polymorphic ventricular tachycardia, an update.
Changes of autonomic information flow due to idiopathic dilated cardiomyopathy.
Clinical and prognostic impact of chronotropic incompetence in patients with hypertrophic cardiomyopathy.
Clinical characteristics of unexplained sudden cardiac death in Korea.
Clinical management and prevention of sudden cardiac death.
Clinical management of ventricular tachycardia.
Clinical significance of new-onset atrial fibrillation in patients with hypertrophic cardiomyopathy.
Common Variants in Cardiac Ion Channel Genes Are Associated with Sudden Cardiac Death.
Congenital short QT syndrome. A review.
Coronary artery disease in athletes: An adverse effect of intense exercise?
Cost-effectiveness of in-home automated external defibrillators for individuals at increased risk of sudden cardiac death.
Current controversies in pre-participation cardiovascular screening for young competitive athletes.
Determinants of patient survival rate after implantation of a cardioverter-defibrillator without resynchronisation capability.
Diabetes and the Risk of Sudden Cardiac Death.
Diagnostic findings and follow-up outcomes in relatives to young non-autopsied sudden death victims.
Dialysis modality-related disparities in sudden cardiac death: hemodialysis versus peritoneal dialysis.
Dietary fat quality and risk of sudden cardiac death in women.
Domperidone and ventricular arrhythmia or sudden cardiac death: a population-based case-control study in the Netherlands.
Early Repolarisation Changes in ECG: Are they Benign or Malignant?
ECG Quantification of Myocardial Scar and Risk Stratification in MADIT-II.
Editorial Comment: Highly sensitive troponin assay and sudden cardiac death in the community Unlocking the pathophysiology of SCD one biomarker at a time.
Effect of Gender and Genetic Mutations on Outcomes in Patients With Hypertrophic Cardiomyopathy.
Electrocardiographic patterns and systolic and diastolic functions of the heart in the highly trained football players with increased left ventricular mass.
Elevated plasma free fatty acids are associated with sudden death: A prospective community-based evaluation at the time of cardiac arrest.
Epidemiology and genetics of ventricular fibrillation during acute myocardial infarction.
Evidence regarding clinical use of microvolt T-wave alternans.
Exercise and Inherited Arrhythmias.
Exercise related sudden cardiac death (SCD) in the young - Pre-mortal characterization of a Swedish nationwide cohort, showing a decline in SCD among athletes.
Family history and the risk of sudden cardiac death as a manifestation of an acute coronary event.
Fibroblast Growth Factor 23 and Sudden Versus Non-sudden Cardiac Death: The Cardiovascular Health Study.
Fragmented ECG as a risk marker in cardiovascular diseases.
Genetic predisposition to sudden cardiac death.
Genetic Variants Are Not Rare in ICD Candidates with Dilated Cardiomyopathy: Time for Next-Generation Sequencing?
Genetic Variants Associated With Unexplained Sudden Cardiac Death in Adult White and African American Individuals.
Heart failure as a substrate and trigger for ventricular tachycardia.
Heart rate variability analysis based on time-frequency representation and entropies in hypertrophic cardiomyopathy patients.
Heart Rate Variability Analysis to Predict Onset of Ventricular Tachyarrhythmias in Implantable Cardioverter Defibrillators.
Hemopexin dosing improves cardiopulmonary dysfunction in murine sickle cell disease.
Hidden Markov Models and Mutual Information Analysis to Characterize Nonlinear Dynamics in Heart Rate Variability.
High prevalence of early repolarization in the paediatric relatives of sudden arrhythmic death syndrome victims and in normal controls.
Histopathology of the conduction system in sudden death from coronary heart disease.
Identification of patients at risk of sudden cardiac death in congenital heart disease: The PRospEctiVE study on implaNTable cardIOverter defibrillator therapy and suddeN cardiac death in Adults with Congenital Heart Disease (PREVENTION-ACHD).
Implantable cardioverter defibrillators in patients with valvular cardiomyopathy.
Implications of multiple late gadolinium enhancement lesions on the frequency of left ventricular reverse remodeling and prognosis in patients with non-ischemic cardiomyopathy.
Improving Clinical Translation of Machine Learning Approaches Through Clinician-Tailored Visual Displays of Black Box Algorithms: Development and Validation.
Inappropriate implantable cardioverter defibrillator discharge from sensing of external alternating current leak.
Incidence, Predictors, and Outcomes of Implantable Cardioverter-Defibrillator Discharge Among People Living With HIV.
Incidence, predictors, and temporal trends of sudden cardiac death after heart transplantation.
Inherited Arrhythmia Syndrome Predisposing to Sudden Cardiac Death.
Intrahospital sudden cardiac death (SCD) at internal medicine clinic of University Clinical Hospital Mostar.
Late gadolinium enhancement on cardiac magnetic resonance predicts adverse cardiovascular outcomes in nonischemic cardiomyopathy: a systematic review and meta-analysis.
Long-term outcome of conservative and invasive treatment in patients with hypertrophic obstructive cardiomyopathy.
Long-term prognostic assessment of ventricular tachycardia with respect to sudden death in patients with and without overt heart disease.
Low heart rate variability is a risk factor for sudden cardiac death in type 2 diabetes.
Management and outcomes of hypertrophic cardiomyopathy in young adults.
Mapping and ablation procedures for the treatment of ventricular tachycardia.
Mechanism and prediction of sudden cardiac death in arrhythmia patients using electrophysiological studies.
Microvolt T-wave alternans and autonomic nervous system parameters can be helpful in the identification of low-arrhythmic risk patients with ischemic left ventricular systolic dysfunction.
Mild-to-moderate kidney dysfunction and the risk of sudden cardiac death in the setting of acute myocardial infarction.
Mitral Valve Prolapse and Sudden Cardiac Death: A Systematic Review.
Monogenec Arrhythmic Syndromes: From Molecular and Genetic Aspects to Bedside.
Mortality and appropriate and inappropriate therapy in patients with ischaemic heart disease and implanted cardioverter-defibrillators for primary prevention: data from the Danish ICD Register.
Mortality and Sudden Cardiac Death Risk Stratification Using the Noninvasive Combination of Wide QRS Duration and Late Gadolinium Enhancement in Idiopathic Dilated Cardiomyopathy.
Multiple independent genetic factors at NOS1AP modulate the QT interval in a multi-ethnic population.
Myocardial Infarction in Sickle Cell Disease: Use of Translational Imaging to Diagnose an Under-Recognized Problem.
Non-cardiovascular drugs that inhibit hERG-encoded potassium channels and risk of sudden cardiac death.
Novel KCNQ1 mutations in patients after myocardial infarction.
Novel Variants in TECRL Cause Catecholaminergic Polymorphic Ventricular Tachycardia.
Out of hospital sudden cardiac death in Italy: a population-based case-control study.
Phenotypic expression is a prerequisite for malignant arrhythmic events and sudden cardiac death in arrhythmogenic right ventricular cardiomyopathy.
Platelet collagen receptor GPIa (C807T/HPA-5) haplotype is not associated with an increased risk of fatal coronary events in middle-aged men.
Population-based analysis of sudden cardiac death with and without left ventricular systolic dysfunction: two-year findings from the Oregon Sudden Unexpected Death Study.
Post-mortem CMR in a model of sudden death due to myocardial ischemia: validation with connexin-43.
Post-mortem toxicology in young sudden cardiac death victims: A nationwide cohort study.
Preclinical evidence for the therapeutic value of TBX5 normalization in arrhythmia control.
Prediction of appropriate ICD therapy in patients with ischemic heart failure.
Predictors of right ventricular function and size in patients with hypertrophic cardiomyopathy.
Predictors of sudden cardiac death in hypertrophic cardiomyopathy.
Predictors of sudden cardiac death.
Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases.
Preventing tomorrow's sudden cardiac death today: dissemination of effective therapies for sudden cardiac death prevention.
Prevention of sudden cardiac death in patients with chronic kidney disease.
Prevention of sudden cardiac death.
Prognostic impact of misdiagnosis of cardiac channelopathies as epilepsy.
Prognostic impact of multiple fragmented QRS on cardiac events in idiopathic dilated cardiomyopathy.
Prophylactic implantable cardioverter defibrillator trials: MUSTT, MADIT, and beyond. Multicenter Unsustained Tachycardia Trial. Multicenter Automatic Defibrillator Implantation Trial.
Prospective Countywide Surveillance and Autopsy Characterization of Sudden Cardiac Death: POST SCD Study.
Prospective study of sudden cardiac death among women in the United States.
QT interval dispersion in healthy subjects and survivors of sudden cardiac death: circadian variation in a twenty-four-hour assessment.
Rate-dependent electrical, contractile and restitution properties of isolated left ventricular myocytes in guinea-pig hypertrophy.
Rationale and design of the Pan-African Sudden Cardiac Death survey: the Pan-African SCD study.
Regional differences in incidence of sudden cardiac death in the young.
Relation of Body Mass Index Categories with Risk of Sudden Cardiac Death.
Relationship of LVEF and Myocardial Scar to Long-Term Mortality Risk and Mode of Death in Patients With Nonischemic Cardiomyopathy.
Repolarization abnormalities and afterdepolarizations in a canine model of sudden cardiac death.
Ring-like late gadolinium enhancement for predicting ventricular tachyarrhythmias in non-ischaemic dilated cardiomyopathy.
Risk factors for cardiac events in patients with Brugada syndrome: A PRISMA-compliant meta-analysis and systematic review.
Risk factors for sudden cardiac death in post-menopausal women.
Risk Models for Prediction of Implantable Cardioverter-Defibrillator Benefit: Insights From the DANISH Trial.
Risk stratification for sudden cardiac death in dilated cardiomyopathy using microvolt-level T-wave alternans.
Risk Stratification for Sudden Cardiac Death.
Risk stratification using late gadolinium enhancement on cardiac magnetic resonance imaging in patients with hypertrophic cardiomyopathy: A systematic review and meta-analysis.
Risk stratifiers for sudden cardiac death (SCD) in the community: primary prevention of SCD.
Role of echocardiography in screening and evaluation of athletes.
Serum transforming growth factor-beta1 as a risk stratifier of sudden cardiac death.
Sex-specific differences in outcome and risk stratification of ventricular arrhythmias in implantable cardioverter defibrillator patients.
Should Primary Prevention ICDs Still Be Placed in Patients with Non-ischemic Cardiomyopathy? A Review of the Evidence.
Sinergy between drugs and devices in the fight against sudden cardiac death and heart failure.
Structural pathways and prevention of heart failure and sudden death.
Sudden cardiac death - Historical perspectives.
Sudden cardiac death and coronary disease in the young: A nationwide cohort study in Denmark.
Sudden cardiac death following liver transplantation: Incidence, trends and risk predictors.
Sudden cardiac death in athletes.
Sudden Cardiac Death in Athletes.
Sudden cardiac death in dialysis patients: different causes and management strategies.
Sudden cardiac death in heart failure patients with preserved ejection fraction.
Sudden Cardiac Death in India: A Growing Concern.
Sudden cardiac death in patients with silent myocardial ischemia after myocardial infarction (from the Swiss Interventional Study on Silent Ischemia Type II [SWISSI II]).
Sudden cardiac death in patients with stable coronary artery disease and preserved left ventricular systolic function.
Sudden cardiac death in post myocardial infarction patients.
Sudden cardiac death in the young.
Sudden Cardiac Death in Women With Suspected Ischemic Heart Disease, Preserved Ejection Fraction, and No Obstructive Coronary Artery Disease: A Report From the Women's Ischemia Syndrome Evaluation Study.
Sudden Cardiac Death in Women.
Sudden cardiac death in young athletes; a literature review and special considerations in Asia.
Sudden cardiac death rates in an Australian population: a data linkage study.
Sudden cardiac death: Beware of hasty diagnosis!
Sudden death and its predictors in myocardial infarction survivors in an Indian population.
Sudden death in children and adolescents.
Sudden death mortality in implantable cardioverter defibrillator patients.
Supraventricular Arrhythmias in Patients with Adult Congenital Heart Disease.
TED-Time and life saving External Defibrillator for home-use.
Temporal trends and sex differences in sudden cardiac death in the Copenhagen City Heart Study.
Temporal variability of T-wave morphology and risk of sudden cardiac death in patients with coronary artery disease.
Ten advances defining sudden cardiac death.
The 12-lead electrocardiogram of the elite female footballer as defined by different interpretation criteria across the competitive season.
The autopsy study of 553 cases of sudden cardiac death in Chinese adults.
The Burden of Sudden Cardiac Death in Persons Aged 1-49 Years - A Nationwide Study in Denmark.
The diagnosis and management of short QT syndrome.
The European Myocardial Infarct Amiodarone Trial (EMIAT). EMIAT Investigators.
The Hidden Fragility in the Heart of the Athletes: A Review of Genetic Biomarkers.
The J wave and fragmented QRS complexes in inferior leads associated with sudden cardiac death in patients with chronic heart failure.
The sex gap in hypertrophic cardiomyopathy.
Time-frequency analysis of ECG for late potentials in sudden cardiac death survivors and post-myocardial infarction patients.
Tools for risk stratification of sudden cardiac death: A review of the literature in different patient populations.
Towards cardiac MRI based risk stratification in idiopathic dilated cardiomyopathy.
Type 1 Brugada pattern electrocardiogram induced by hypokalemia.
Type 2 diabetes and coronary artery disease: Preserved ejection fraction and sudden cardiac death.
Usefulness of Electrocardiographic Patterns at Presentation to Predict Long-term Risk of Cardiac Death in Patients With Hypertrophic Cardiomyopathy.
Usefulness of the Duke Sudden Cardiac Death risk score for predicting sudden cardiac death in patients with angiographic (>75% narrowing) coronary artery disease.
Validation of the 2020 AHA/ACC Risk Stratification for Sudden Cardiac Death in Chinese Patients With Hypertrophic Cardiomyopathy.
Ventricular tachycardia-inducibility predicts arrhythmic events in post-myocardial infarction patients with low ejection fraction. A systematic review and meta-analysis.
Verification of Single Nucleotide Polymorphisms rs34554140, rs6670279, and rs6874185 as Novel Molecular Genetic Markers of Sudden Cardiac Death.
[Antiarrhythmic agents in the prevention of sudden cardiac death]
[Feasibility of the 2014 European guidelines risk prediction model for sudden cardiac death in hypertrophic cardiomyopathy in Chinese patients].
[Heart Rate Turbulence and T-Wave Alternans as Markers of Risk of Sudden Cardiac Death in Patients With Hypertrophic Cardiomyopathy.]
[Primary prevention of sudden cardiac death implanted cardioverter defibrillator (ICD) versus antiarrhythmic drugs]
[Relationship between arrhythmia profile, left ventricular function and sudden death in the post-infarct period of patients resuscitated from heart arrest]
[Screening of athletes is undesirable].
[Sudden cardiac death (SCD) and guidelines for SCD]
[Sudden cardiac death : Epidemiology, pathophysiology and risk stratification].
[Sudden cardiac death and automated external defibrillators. Where we are in 2012?].
[Sudden cardiac death: medico-legal aspects]
[Sudden cardiac death: state of the art]
[The advance in study of sudden cardiac death mechanism]
[The use of implantable cardioverter-defibrillators in patients at high risk of sudden cardiac death.]
[Toll-like receptor 4 expression in the coronary atherosclerotic plaques of patients died from sudden cardiac death]
[Ventricular tachycardia : Treatment and prognostic significance].
[Worldwide experience with automated external defibrillators : What have we achieved? What else can we expect?].
Deglutition Disorders
[Videofluorographic analysis of the swallowing disorders in spinocerebellar degeneration]
Dehydration
Cation Homeostasis in Red Cells From Patients With Sickle Cell Disease Heterologous for HbS and HbC (HbSC Genotype).
Correction of sickle cell disease in transgenic mouse models by gene therapy.
Dehydration, rehydration, and overhydration alter patterns of gene expression in the Antarctic midge, Belgica antarctica.
Effects of 5-hydroxymethyl-2-furfural on the volume and membrane permeability of red blood cells from patients with sickle cell disease.
New Therapeutic Options for the Treatment of Sickle Cell Disease.
Pathophysiology and recent therapeutic insights of sickle cell disease.
Prevalence and factors associated with renal dysfunction in children admitted to two hospitals in northwestern Tanzania.
Sickle cell nephropathy: challenging the conventional wisdom.
Sudden cardiac death in football.
The effect of deoxygenation on whole-cell conductance of red blood cells from healthy individuals and patients with sickle cell disease.
The super sickling haemoglobin HbS-Oman: a study of red cell sickling, K(+) permeability and associations with disease severity in patients heterozygous for HbA and HbS-Oman (HbA/S-Oman genotype).
Urinary endothelin-1 as a marker of renal damage in sickle cell disease.
Dementia
A comparative study on the validations of three cognitive screening tests in identifying subtle cognitive decline.
A Homeostatic Model of Subjective Cognitive Decline.
A more randomly organized grey matter network is associated with deteriorating language and global cognition in individuals with subjective cognitive decline.
A Validation Study of the Inbrain CST: a Tablet Computer-based Cognitive Screening Test for Elderly People with Cognitive Impairment.
Advanced Circadian Timing and Sleep Fragmentation Differentially Impact on Memory Complaint Subtype in Subjective Cognitive Decline.
Affective symptoms and risk of progression to mild cognitive impairment or dementia in subjective cognitive decline: A systematic review and meta-analysis.
Amyloid-? misfolding as a plasma biomarker indicates risk for future clinical Alzheimer's disease in individuals with subjective cognitive decline.
Anxiety and depression symptoms among caregivers of care-recipients with subjective cognitive decline and cognitive impairment.
Association Between Cognitive Test Performance and Subjective Cognitive Decline in a Diverse Cohort of Older Adults: Findings From the KHANDLE Study.
Association Between Later Life Lifestyle Factors and Alzheimer's Disease Biomarkers in Non-Demented Individuals: A Longitudinal Descriptive Cohort Study.
Association of Subjective Cognitive Decline with Risk of Cognitive Impairment and Dementia: A Systematic Review and Meta-Analysis of Prospective Longitudinal Studies.
ATN classification and clinical progression in subjective cognitive decline: The SCIENCe project.
Auditory Verbal Learning Test is Superior to Rey-Osterrieth Complex Figure Memory for Predicting Mild Cognitive Impairment to Alzheimer's Disease.
Balance and Mobility Performance Along the Alzheimer's Disease Spectrum.
Basal Forebrain Atrophy Is Associated With Allocentric Navigation Deficits in Subjective Cognitive Decline.
Blood Pressure in Different Dementia Disorders, Mild Cognitive Impairment, and Subjective Cognitive Decline.
Brain atrophy and patch-based grading in individuals from the CIMA-Q study: a progressive continuum from subjective cognitive decline to AD.
Brain connectivity and metacognition in persons with subjective cognitive decline (COSCODE): rationale and study design.
Brain Network Integrity Changes in Subjective Cognitive Decline: A Possible Physiological Biomarker of Dementia.
Cerebrospinal Fluid Biomarkers and Clinical Progression in Patients with Subjective Cognitive Decline and Mild Cognitive Impairment.
Cerebrospinal Fluid Biomarkers Predict Clinical Evolution in Patients with Subjective Cognitive Decline and Mild Cognitive Impairment.
Cerebrospinal fluid N-224 tau helps discriminate Alzheimer's disease from subjective cognitive decline and other dementias.
Clinical impact of [18F]flutemetamol PET among memory clinic patients with an unclear diagnosis.
Cognitive performance before and after the onset of subjective cognitive decline in old age.
Correlates of Subjective Cognitive Decline in Lesbian, Gay, Bisexual, and Transgender Older Adults.
Depression and APOE?4 Status in Individuals with Subjective Cognitive Decline: A Meta-Analysis.
Depression, subjective cognitive decline, and the risk of neurocognitive disorders.
Design and first baseline data of the DZNE multicenter observational study on predementia Alzheimer's disease (DELCODE).
Different Cortical Thinning Patterns Depending on Their Prognosis in Individuals with Subjective Cognitive Decline.
Differential Impact of Cigarette Smoking on Fracture Risks in Subjective Cognitive Decline and Dementia: A Nationwide Longitudinal Study.
Differential Risk of Incident Alzheimer's Disease Dementia in Stable Versus Unstable Patterns of Subjective Cognitive Decline.
Differential Risk of Incident Fractures Depending on Intensity and Frequency of Physical Activity According to Cognitive Status: A Nationwide Longitudinal Study.
Discordant amyloid-? PET and CSF biomarkers and its clinical consequences.
Discriminant Validity of the WAIS-R Digit Symbol Substitution Test in Subjective Cognitive Decline, Mild Cognitive Impairment (Amnestic Subtype) and Alzheimer's Disease Dementia (ADD) in Greece.
Does Empirically Derived Classification of Individuals with Subjective Cognitive Complaints Predict Dementia?
Effects of spermidine supplementation on cognition and biomarkers in older adults with subjective cognitive decline (SmartAge)-study protocol for a randomized controlled trial.
Ego- and allo-network disconnection underlying spatial disorientation in subjective cognitive decline.
Enhancing 'meaningfulness' of functional assessments: UK adaptation of the Amsterdam IADL questionnaire.
Estimating Dementia and Receipt of Informal Care Using Behavioral Risk Factor Surveillance System Data.
Estimating prevalence of subjective cognitive decline in and across international cohort studies of aging: a COSMIC study.
Factors Predicting the Onset of Amnestic Mild Cognitive Impairment or Alzheimer's Dementia in Persons With Subjective Cognitive Decline.
Frailty Is Related to Subjective Cognitive Decline in Older Women without Dementia.
Functional cognitive disorder in subjective cognitive decline-A 10-year follow-up.
Glial activation and inflammation along the Alzheimer's disease continuum.
Glucose metabolism in the right middle temporal gyrus could be a potential biomarker for subjective cognitive decline: a study of a Han population.
Gradual Disturbances of the Amplitude of Low-Frequency Fluctuations (ALFF) and Fractional ALFF in Alzheimer Spectrum.
Impact of a clinical decision support tool on prediction of progression in early-stage dementia: a prospective validation study.
Increased Risk of Dementia in Subjective Cognitive Decline if CT Brain Changes are Present.
Is brain connectome research the future frontier for subjective cognitive decline? A systematic review.
Is function in instrumental activities of daily living a useful feature in predicting Alzheimer's disease dementia in subjective cognitive decline?
Late-life depression, subjective cognitive decline, and their additive risk in incidence of dementia: A nationwide longitudinal study.
Localized Analysis of Normalized Distance from Scalp to Cortex and Personalized Evaluation (LANDSCAPE): Focusing on Age- and Dementia-Specific Changes.
Longitudinal Cognitive Profiles by Anxiety and Depressive Symptoms in American Older Adults With Subjective Cognitive Decline.
Lower cerebral blood flow in subjects with Alzheimer's dementia, mild cognitive impairment, and subjective cognitive decline using two-dimensional phase-contrast magnetic resonance imaging.
Lower cerebral blood flow is associated with impairment in multiple cognitive domains in Alzheimer's disease.
Mediterranean Diet, Alzheimer Disease Biomarkers and Brain Atrophy in Old Age.
Memory Complaints and Cognitive Decline: Data from the GUIDAGE Study1.
Memory complaints at primary care in a middle-income country: clinical and neuropsychological characterization.
Mild Behavioral Impairment and Subjective Cognitive Decline Predict Cognitive and Functional Decline.
Multisensory, Multi-Tasking Performance of Older Adults With and Without Subjective Cognitive Decline.
Neuroimaging advances regarding subjective cognitive decline in preclinical Alzheimer's disease.
Neuropsychiatric and Cognitive Symptoms Across the Alzheimer Disease Clinical Spectrum: Cross-sectional and Longitudinal Associations.
Neuropsychiatric symptoms in at-risk groups for AD dementia and their association with worry and AD biomarkers-results from the DELCODE study.
Neuropsychological predictors of cognitive deterioration in non-demented individuals.
Normative Data for the Montreal Cognitive Assessment in Greek Older Adults With Subjective Cognitive Decline, Mild Cognitive Impairment and Dementia.
Objective features of subjective cognitive decline in a United States national database.
Orthostatic Hypotension: An Important Risk Factor for Clinical Progression to Mild Cognitive Impairment or Dementia. The Amsterdam Dementia Cohort.
Outcomes of stable and unstable patterns of subjective cognitive decline - results from the Leipzig Longitudinal Study of the Aged (LEILA75+).
PET and CSF amyloid-? status are differently predicted by patient features: information from discordant cases.
Physical activity for cognitive health: what advice can we give to older adults with subjective cognitive decline and mild cognitive impairment?
Physical performance across the cognitive spectrum and between dementia subtypes in a population-based sample of older adults: The HUNT study.
Plasma Amyloid as Prescreener for the Earliest Alzheimer Pathological Changes.
Plasma NT1 Tau is a Specific and Early Marker of Alzheimer's Disease.
Plasma Protein Biomarkers for the Prediction of CSF Amyloid and Tau and [18F]-Flutemetamol PET Scan Result.
Population measures of subjective cognitive decline: A means of advancing public health policy to address cognitive health.
Prediction of dementia of Alzheimer type by different types of subjective cognitive decline.
Prevalence and determinants of subjective cognitive decline in a representative Greek elderly population.
Prevalence of abnormal Alzheimer's disease biomarkers in patients with subjective cognitive decline: cross-sectional comparison of three European memory clinic samples.
REMEDES for Alzheimer-R4Alz Battery: Design and Development of a New Tool of Cognitive Control Assessment for the Diagnosis of Minor and Major Neurocognitive Disorders.
Repetitive negative thinking is associated with subjective cognitive decline in older adults: a cross-sectional study.
Results and their implications from comparing respondents and proxy responses for non-respondents with cognitive difficulties on a telephone survey.
Risk Factors and Neuropsychological Assessments of Subjective Cognitive Decline (plus) in Chinese Memory Clinic.
Risk of progression from subjective cognitive decline to mild cognitive impairment: The role of study setting.
Scalp-to-cortex distance of left primary motor cortex and its computational head model: Implications for personalized neuromodulation.
Screening for Cognitive Dysfunction Using the Rowland Universal Dementia Assessment Scale in Adults With Sickle Cell Disease.
Screening for cognitive impairment in an Australian aged care assessment team as part of comprehensive geriatric assessment.
Screening for Mild Cognitive Impairment and Dementia with Automated, Anonymous Online and Telephone Cognitive Self-Tests.
Sex differences in CSF biomarkers vary by Alzheimer's disease stage and APOE ?4 genotype.
Smaller medial temporal lobe volumes in individuals with subjective cognitive decline and biomarker evidence of Alzheimer's disease-Data from three memory clinic studies.
Specific Nutritional Biomarker Profiles in Mild Cognitive Impairment and Subjective Cognitive Decline Are Associated With Clinical Progression: The NUDAD Project.
Spinocerebellar degeneration (SCD): cognitive disturbances.
Structural integrity in subjective cognitive decline, mild cognitive impairment and Alzheimer's disease based on multicenter diffusion tensor imaging.
Subjective and objective cognitive decline at the pre-dementia stage of Alzheimer's disease.
Subjective cognitive complaints at age 70: associations with amyloid and mental health.
Subjective Cognitive Decline and APOE ?4: A Systematic Review.
Subjective Cognitive Decline and its Relation to Verbal Memory and Sex in Cognitively Unimpaired Individuals from a Colombian Cohort with Autosomal-Dominant Alzheimer's Disease.
Subjective Cognitive Decline and Nighttime Sleep Alterations, a Longitudinal Analysis.
Subjective cognitive decline and objective cognition among diverse U.S. Hispanics/Latinos: Results from the Study of Latinos-Investigation of Neurocognitive Aging (SOL-INCA).
Subjective cognitive decline and progression to dementia in Parkinson's disease: a long-term follow-up study.
Subjective cognitive decline and rates of incident Alzheimer's disease and non-Alzheimer's disease dementia.
Subjective cognitive decline and subsequent dementia: a nationwide cohort study of 579,710 people aged 66 years in South Korea.
Subjective cognitive decline as a predictor of future cognitive decline: a systematic review.
Subjective Cognitive Decline May Be a Stronger Predictor of Incident Dementia in Women than in Men.
Subjective cognitive decline, anxiety symptoms, and the risk of mild cognitive impairment and dementia.
Subjective Spatial Navigation Complaints - A Frequent Symptom Reported by Patients with Subjective Cognitive Decline, Mild Cognitive Impairment and Alzheimer's Disease.
Targeting Cognitive Frailty: Clinical and Neurobiological Roadmap for a Single Complex Phenotype.
Tau plasma levels in subjective cognitive decline: Results from the DELCODE study.
tDCS-Induced Memory Reconsolidation Effects and Its Associations With Structural and Functional MRI Substrates in Subjective Cognitive Decline.
The characterisation of subjective cognitive decline.
The ERICA Score: An MR Imaging-based Visual Scoring System for the Assessment of Entorhinal Cortex Atrophy in Alzheimer Disease.
The frequency of sleep medication use and the risk of subjective cognitive decline (SCD) or SCD with functional difficulties in elderly individuals without dementia.
The Impact of the Virtual Cognitive Health Program on the Cognition and Mental Health of Older Adults: Pre-Post 12-Month Pilot Study.
The Power of EEG to Predict Conversion from Mild Cognitive Impairment and Subjective Cognitive Decline to Dementia.
The Relationship between Subjective Cognitive Decline and Health Literacy in Healthy Community-Dwelling Older Adults.
The SCD-Well randomized controlled trial: Effects of a mindfulness-based intervention versus health education on mental health in patients with subjective cognitive decline (SCD).
Thinner cortex in patients with subjective cognitive decline is associated with steeper decline of memory.
Thinner temporal and parietal cortex is related to incident clinical progression to dementia in patients with subjective cognitive decline.
Use of Cerebrospinal Fluid Biomarkers of Alzheimer's Disease Risk in Mild Cognitive Impairment and Subjective Cognitive Decline in Routine Clinical Care in Germany.
Visual impairment in aging and cognitive decline: experience in a Memory Clinic.
What are subjective cognitive difficulties and do they matter?
[From mild cognitive impairment to dementia: what is the role of public health?]
[Memory dysfunction of spinocerebellar degeneration]
[Subjective Cognitive Decline and Development of Dementia - Results from the Leipzig Longitudinal Study of the Aged (LEILA75+)].
Demyelinating Diseases
A Case of Subacute Combined Degeneration of the Spinal Cord with Infective Endocarditis.
Oligodendroglia in cortical multiple sclerosis lesions decrease with disease progression, but regenerate after repeated experimental demyelination.
Subacute combined degeneration of the spinal cord in cblC disorder despite treatment with B12.
Dengue
Dengue in hospitalized children with sickle cell disease: A retrospective cohort study in the French departments of America.
Vaso-occlusive crisis in a sickle cell patient after transfusion-transmitted dengue infection.
Dental Caries
Association between sickle cell disease and dental caries: a systematic review and meta-analysis.
Association between sickle cell disease and the oral health condition of children and adolescents.
Caries prevalence and impact on oral health-related quality of life in children with sickle cell disease: cross-sectional study.
Orofacial Manifestations in Patients with Sickle Cell Disease.
Periodontitis and dental caries occur together.
Self-perceived loss of control and untreated dental decay in African American adults with and without sickle cell disease.
The association between dental and periodontal diseases and sickle cell disease. A pilot case-control study.
The association between sickle cell disease and dental caries in African Americans.
The impact of the oral condition of children with sickle cell disease on family quality of life.
Dental Enamel Hypoplasia
Hypodontia in an adolescent with the HbSC genotype: a case report.
Dentin Sensitivity
Post-bleaching sensitivity in patients with sickle cell disease.
Dermatitis
Atopy and Sensitization to Allergens Known to Cause Systemic Contact Dermatitis.
Systemic Contact Dermatitis in Children: How an Avoidance Diet Can Make a Difference.
Systemic contact dermatitis: sometimes it is the food.
Systemic Contact Dermatitis: The Routes of Allergen Entry.
Ulcerative dermatitis in C57BL/6 mice lacking stearoyl CoA desaturase 1.
Dermatitis, Allergic Contact
Metal allergy and systemic contact dermatitis: an overview.
Dermatitis, Atopic
Atopy patch tests may identify patients at risk for systemic contact dermatitis.
Elevated serum levels of soluble CD30 are associated with atopic dermatitis, but not with respiratory atopic disorders and allergic contact dermatitis.
Dermatitis, Contact
Mixed Bullous-Eczematous Contact Dermatitis From a Black Henna Tattoo in an African American Female With Sickle Cell Disease With Post-Dermatitis Pain.
Systemic Contact Dermatitis.
Systemic nickel hypersensitivity and diet: myth or reality?
Dermoid Cyst
Shadow cell differentiation in testicular teratomas. A report of two cases.
Diabetes Insipidus, Nephrogenic
Urinary endothelin-1 as a marker of renal damage in sickle cell disease.
Diabetes Mellitus
Association between Clinical and Doppler Echocardiographic Parameters with Sudden Death in Hemodialysis Patients.
Association between clinical outcomes and metformin use in adults with sickle cell disease and diabetes mellitus.
Association of FADS2 rs174575 gene polymorphism and insulin resistance in type 2 diabetes mellitus.
Biomarkers of Dietary Omega-6 Fatty Acids and Incident Cardiovascular Disease and Mortality.
Cardiorespiratory fitness is related to the risk of sudden cardiac death: a population-based follow-up study.
Depressive symptoms and the risk of sudden cardiac death among the elderly.
Determinants of prolonged QT interval and their contribution to sudden death risk in coronary artery disease: the Oregon Sudden Unexpected Death Study.
Development and Validation of a Sudden Cardiac Death Prediction Model for the General Population.
Electrocardiographic and cardiac magnetic resonance imaging parameters as predictors of a worse outcome in patients with idiopathic dilated cardiomyopathy.
Genetic variants in desaturase gene, erythrocyte fatty acids, and risk for type 2 diabetes in Chinese Hans.
Global Electric Heterogeneity Risk Score for Prediction of Sudden Cardiac Death in the General Population: The Atherosclerosis Risk in Communities (ARIC) and Cardiovascular Health (CHS) Studies.
Left atrial enlargement and NT-proBNP as predictors of sudden cardiac death in patients with heart failure.
Low Potassium Dialysate as a Protective Factor of Sudden Cardiac Death in Hemodialysis Patients with Hyperkalemia.
Mortality in Individuals with Subjective Cognitive Decline: Results of the Leipzig Longitudinal Study of the Aged (LEILA75+).
Obesity and diabetes mellitus in patients with sickle cell disease.
Predictive scores for identifying patients with type 2 diabetes mellitus at risk of acute myocardial infarction and sudden cardiac death.
Recent advances on stearoyl-CoA desaturase regulation in fatty liver diseases.
Reduced expression of stearoyl-CoA desaturase-1, but not free fatty acid receptor 2 or 4 in subcutaneous adipose tissue of patients with newly diagnosed type 2 diabetes mellitus.
Relationship Between Anemia and Sudden Cardiac Death in Patients with Severe Aortic Stenosis.
Remote ischemic preconditioning differentially attenuates post-ischemic cardiac arrhythmia in streptozotocin-induced diabetic versus nondiabetic rats.
Results of Kidney Transplantation from Expanded Criteria Donors: A Single-Center Experience.
Sudden Cardiac Death After Non-ST-Segment Elevation Acute Coronary Syndrome.
Sudden cardiac death and diabetes mellitus.
Sudden Cardiac Death in Hypertensive Patients.
Sudden cardiac death in patients with diabetes.
Sudden Cardiac Death in Women With Suspected Ischemic Heart Disease, Preserved Ejection Fraction, and No Obstructive Coronary Artery Disease: A Report From the Women's Ischemia Syndrome Evaluation Study.
Sudden cardiac death risk prediction in heart failure with preserved ejection fraction.
Sudden Death After Hospitalization for Heart Failure With Reduced Ejection Fraction (from the EVEREST Trial).
Technetium 99m-diethylene triamine penta-acetic acid aerosol clearance in the evaluation of pulmonary involvement in sickle cell disease.
The Contribution of Known Familial Cardiovascular Disease Genes to Sudden Cardiac Death in Patients Undergoing Hemodialysis.
Urgency of Emergency Department Visits by Children With Sickle Cell Disease: A Comparison of 3 Chronic Conditions.
Diabetes Mellitus, Type 1
Desaturase activities in rat model of insulin resistance induced by a sucrose-rich diet.
Diabetes Mellitus, Type 2
Analysis of the contribution to type 2 diabetes susceptibility of sequence variation in the gene encoding stearoyl-CoA desaturase, a key regulator of lipid and carbohydrate metabolism.
Association of FADS2 rs174575 gene polymorphism and insulin resistance in type 2 diabetes mellitus.
Association of Polymorphism in Fatty Acid Desaturase Gene with the Risk of Type 2 Diabetes in Iranian Population.
Cardiorespiratory fitness is related to the risk of sudden cardiac death: a population-based follow-up study.
Discovery and pharmacological characterization of SAR707 as novel and selective small molecule inhibitor of stearoyl-CoA desaturase (SCD1).
Evaluation of various biomarkers as potential mediators of the association between ?5 desaturase, ?6 desaturase, and stearoyl-CoA desaturase activity and incident type 2 diabetes in the European Prospective Investigation into Cancer and Nutrition-Potsdam Study.
FADS Gene Polymorphisms, Fatty Acid Desaturase Activities, and HDL-C in Type 2 Diabetes.
Genetic variants in desaturase gene, erythrocyte fatty acids, and risk for type 2 diabetes in Chinese Hans.
Hepatic delta9, delta6, and delta5 desaturations in non-insulin-dependent diabetes mellitus eSS rats.
Impaired Fasting Plasma Glucose and Type 2 Diabetes Are Related to the Risk of Out-of-Hospital Sudden Cardiac Death and All-Cause Mortality.
Insights into Stearoyl-CoA Desaturase-1 Regulation of Systemic Metabolism.
Joint effect of blood pressure and C-reactive protein and the risk of sudden cardiac death: A prospective cohort study.
Longitudinal associations of serum fatty acid composition with type 2 diabetes risk and markers of insulin secretion and sensitivity in the Finnish Diabetes Prevention Study.
Low heart rate variability is a risk factor for sudden cardiac death in type 2 diabetes.
Modulation of palmitate-induced endoplasmic reticulum stress and apoptosis in pancreatic {beta}-cells by stearoyl-CoA desaturase and Elovl6.
Plasma polyunsaturated fatty acid profile and delta-5 desaturase activity are altered in patients with type 2 diabetes.
Polymorphisms in FADS1 and FADS2 alter plasma fatty acids and desaturase levels in type 2 diabetic patients with coronary artery disease.
Predictive scores for identifying patients with type 2 diabetes mellitus at risk of acute myocardial infarction and sudden cardiac death.
Red Blood Cell Fatty Acids and Incident Diabetes Mellitus in the Women's Health Initiative Memory Study.
Reduced expression of stearoyl-CoA desaturase-1, but not free fatty acid receptor 2 or 4 in subcutaneous adipose tissue of patients with newly diagnosed type 2 diabetes mellitus.
Relation of systemic blood pressure to sudden cardiac death.
Sudden cardiac death after myocardial infarction in patients with type 2 diabetes.
Diabetic Nephropathies
Susceptibility of Podocytes to Palmitic Acid Is Regulated by Stearoyl-CoA Desaturases 1 and 2.
[Arterial hypertension and sudden cardiac death]
[Sudden cardiac death in diabetes mellitus].
Diabetic Neuropathies
Identification of genes and signaling pathways associated with diabetic neuropathy using a weighted correlation network analysis: A consort study.
Diastema
Hypodontia in an adolescent with the HbSC genotype: a case report.
Disorders of Excessive Somnolence
Restless legs syndrome and sleep quality among adult sickle cell disease patients.
Sequential compression devices for treatment of restless legs syndrome.
Diverticulitis
Intraoperative diagnosis of solitary cecal diverticulum not requiring surgery: is appendectomy indicated?
Is there an added value of faecal calprotectin and haemoglobin in the diagnostic work-up for primary care patients suspected of significant colorectal disease? A cross-sectional diagnostic study.
Diverticulum
Left ventricular apical hypoplasia: Case report on cardiomyopathy and a history of sudden cardiac death.
Double Outlet Right Ventricle
Spondylocostal dysostosis with tetralogy of Fallot and herniation of the spleen through the diaphragm.
Dwarfism, Pituitary
Empty sella in short children with and without hypothalamic-pituitary abnormalities.
Growth hormone secretion and circulating insulin-like growth factor-I (IGF-I) and IGF binding protein-3 concentrations in children with sickle cell disease.
Dysarthria
Short-Term Effect of Intensive Speech Therapy on Dysarthria in Patients With Sporadic Spinocerebellar Degeneration.
[Ataxic dysarthria].
Dyskinesias
Nitrous Oxide-induced Subacute Combined Degeneration Presenting with Dystonia and Pseudoathetosis: A Case Report.
Dyslipidemias
A dominant negative form of the transcription factor c-Jun affects genes that have opposing effects on lipid homeostasis in mice.
Association between erythrocyte membrane fatty acids and biomarkers of dyslipidemia in the EPIC-Potsdam study.
Development of a Liver-Targeted Stearoyl-CoA Desaturase (SCD) Inhibitor (MK-8245) to Establish a Therapeutic Window for the Treatment of Diabetes and Dyslipidemia.
Discovery and pharmacological characterization of SAR707 as novel and selective small molecule inhibitor of stearoyl-CoA desaturase (SCD1).
Dyslipidemia and atherosclerosis induced by chronic intermittent hypoxia are attenuated by deficiency of stearoyl coenzyme A desaturase.
Efficacy of habitual exercise for improving lipid profiles depends on the PPRA? genotype in Japanese males.
Evaluation of various biomarkers as potential mediators of the association between ?5 desaturase, ?6 desaturase, and stearoyl-CoA desaturase activity and incident type 2 diabetes in the European Prospective Investigation into Cancer and Nutrition-Potsdam Study.
Long-term administration of olanzapine induces adiposity and increases hepatic fatty acid desaturation protein in female C57BL/6J mice.
Obstructive sleep apnea and dyslipidemia: evidence and underlying mechanism.
Recent Advances in Stearoyl-CoA Desaturase 1 Inhibitors for Dyslipidemia and Obesity.
Sudden death in schizophrenia.
The role of the small intestine in modulating metabolism and inflammation in atherosclerosis and cancer.
[Effect of quercetin on the expression of the carbohydrate and lipid metabolism genes in the liver of rats with genetic].
[Lipid, lipoproteins and atherogenesis profiles in sickle cell disease among Central African patients].
Dyspareunia
Dyspareunia is associated with chronic pain in premenopausal women with sickle cell disease.
Dyspnea
Abnormal Ventilation-Perfusion Scan Is Associated with Pulmonary Hypertension in Sickle Cell Adults.
COVID-19 Presentation in Patients with Sickle Cell Disease: A Case Series.
Decreased exhaled nitric oxide in sickle cell disease: relationship with chronic lung involvement.
Dyspnea, pulmonary function and exercise capacity in adult Saudi patients with sickle cell disease.
Effects of home-based inspiratory muscle training on sickle cell disease (SCD) patients.
Non-atherosclerotic coronary artery disease associated with sudden cardiac death.
Patients with anomalous aortic origin of the coronary artery remain at risk after surgical repair.
Symptoms Before Sudden Arrhythmic Death Syndrome: A Nationwide Study Among the Young in Denmark.
The prevalence of abnormal leukocyte count, and its predisposing factors, in patients with sickle cell disease in Saudi Arabia.
Which Febrile Children with Sickle Cell Disease Need a Chest X-Ray?
Dystonia
Nitrous Oxide-induced Subacute Combined Degeneration Presenting with Dystonia and Pseudoathetosis: A Case Report.
[Effect of a complex treatment, including glutargin and erbisol on the blood plasma content of protein P53, apoptotic markers of type II, activity of caspases and the level of sCD 117 in patients with autonomic-vascular dystonia]
Ear Diseases
Are Patients with Spontaneous CSF Otorrhea and Superior Canal Dehiscence Congenitally Predisposed to Their Disorders?
Otological burdens of Nigerian children with sickle cell disease.
Vestibular Evoked Myogenic Potential (VEMP) Testing for Diagnosis of Superior Semicircular Canal Dehiscence.
Vestibular-evoked myogenic potentials in the diagnosis of superior canal dehiscence syndrome.
Eclampsia
Improvement of maternal and fetal outcomes in women with sickle cell disease treated with early prophylactic erythrocytapheresis.
Perinatal implications of sickle cell disease.
Pregnancy outcomes in women with sickle-cell disease in low and high income countries: a systematic review and meta-analysis.
Sickle cell anemia/sickle cell disease and pregnancy outcomes among ethnic tribes in India: an integrative mini-review.
Sickle cell disease and pregnancy outcomes: population-based study on 8.8 million births.
Sickle cell disease in pregnancy: maternal complications in a medicaid-enrolled population.
The emerging challenge of optimal blood pressure management and hypertensive syndromes in pregnant women with sickle cell disease: a review.
Eisenmenger Complex
Determinants of Sudden Cardiac Death in Adult Patients With Eisenmenger Syndrome.
Embolic Stroke
Modes of death and clinical outcomes in adult patients with hypertrophic cardiomyopathy in Thailand.
Usefulness of Electrocardiographic Patterns at Presentation to Predict Long-term Risk of Cardiac Death in Patients With Hypertrophic Cardiomyopathy.
Embolism, Fat
Bone marrow necrosis in sickle cell disease: a description of three cases and a review of the literature.
Integrating Fat Embolism Syndrome Scoring Indices in Sickle Cell Disease: A Practice Management Review.
Encephalomyelitis
Increased Meningeal T and Plasma Cell Infiltration is Associated with Early Subpial Cortical Demyelination in Common Marmosets with Experimental Autoimmune Encephalomyelitis.
Oligodendroglia in cortical multiple sclerosis lesions decrease with disease progression, but regenerate after repeated experimental demyelination.
Encephalomyelitis, Autoimmune, Experimental
Increased Meningeal T and Plasma Cell Infiltration is Associated with Early Subpial Cortical Demyelination in Common Marmosets with Experimental Autoimmune Encephalomyelitis.
Oligodendroglia in cortical multiple sclerosis lesions decrease with disease progression, but regenerate after repeated experimental demyelination.
End Stage Liver Disease
Liver transplantation in children with sickle-cell disease.
Endocarditis
Perioperative Endocarditis Management in a Patient with Homozygous Sickle Cell Disease.
The role of endocarditis in sudden cardiac death: highlighting the value of the autopsy, pathological features and cardiac complications.
Endocarditis, Bacterial
The Risk of Sudden Cardiac Death in Mitral Valve Prolapse: Are All Patients Created Equal?
Endometrial Neoplasms
Targeting stearoyl-CoA desaturase 1 to repress endometrial cancer progression.
Enteritis
Practice patterns and clinical significance of use of capsule endoscopy in suspected and established Crohn's disease.
Enuresis
Nocturnal enuresis and psychosocial problems in pediatric sickle cell disease and sibling controls.
Nocturnal enuresis in pediatric sickle cell disease.
Nocturnal enuresis in sickle cell disease and thalassemia major: associated factors in a clinical sample.
Prevalence of enuresis and its impact in quality of life of patients with sickle cell disease.
Sleep patterns in pediatric sickle cell disease.
Urinary Bladder Dysfunction in Transgenic Sickle Cell Disease Mice.
Eosinophilia
House Dust Mite-Induced Allergic Lung Inflammation Is Not Exacerbated in Sickle Cell Disease Mice.
Epilepsies, Myoclonic
[Study on argyrophilic inclusions of multisystem atrophy (Oppenheimer)]
Epilepsies, Partial
[Topographic analysis of interictal spikes in the presurgical evaluation of severe partial epilepsy]
Epilepsy
A Common Missense Variant in the Neuregulin1 Gene is associated with Both Schizophrenia and Sudden Cardiac Death.
Adverse neurological outcomes in Nigerian children with sickle cell disease.
Analysis of MEG signals of spreading cortical depression with propagation constrained to a rectangular cortical strip. II. Gyrencephalic swine model.
Differential Methylation in the GSTT1 Regulatory Region in Sudden Unexplained Death and Sudden Unexpected Death in Epilepsy.
Febrile seizures prior to sudden cardiac death: a Danish nationwide study.
Neurologic complications in children under five years with sickle cell disease.
Seizures in the Jamaica cohort study of sickle cell disease.
Seizures risk factors in sickle cell disease. The cooperative study of sickle cell disease.
Significance of automated external defibrillator in identifying lethal ventricular arrhythmias.
Sudden cardiac death in children and young adults without structural heart disease: a comprehensive review.
Too long or too short? New insights into abnormal cardiac repolarization in people with chronic epilepsy and its potential role in sudden unexpected death.
Underestimation of sudden deaths among patients with seizures and epilepsy.
Epistaxis
Bleeding in patients with sickle cell disease: a population-based study.
Erectile Dysfunction
Men with sickle cell disease experience greater sexual dysfunction when compared with men without sickle cell disease.
Priapism and Sickle Cell Disease: Special Considerations in Etiology, Management, and Prevention.
Priapism in Homozygous Sickle Cell Patients: Important Clinical and Laboratory Associations.
Reproductive issues in sickle cell disease.
Testosterone induced priapism in two adolescents with sickle cell disease.
Erythema
Contact dermatitis as a systemic disease.
Erythema Infectiosum
In vivo production of type 1 cytokines in healthy sickle cell disease patients.
Parvovirus B19 infection in children with sickle cell disease in the hydroxyurea era.
Parvovirus B19 infection in sickle cell disease: An analysis from the Centers for Disease Control haemoglobinopathy blood surveillance project.
Simultaneous acute splenic sequestration and transient aplastic crisis in children with sickle cell disease.
[Human parvovirus B19 infection in sickle cell disease patients. A two siblings report].
Esophageal Neoplasms
Sulforaphene inhibits esophageal cancer progression via suppressing SCD and CDH3 expression, and activating the GADD45B-MAP2K3-p38-p53 feedback loop.
Euthyroid Sick Syndromes
Clinical characteristics and long-term prognosis of ischemic and non-ischemic cardiomyopathy.
Exanthema
Diagnostic and treatment difficulties in systemic lupus erythematosus coexisting with sickle cell disease.
Eye Diseases
Changes in the cornea related to sickle cell disease: a pilot investigation.
Stearoyl-CoA desaturase inhibitors: update on patented compounds.
Eye Hemorrhage
Bleeding in patients with sickle cell disease: a population-based study.
Fanconi Anemia
Cell and Gene Therapy for Anemia: Hematopoietic Stem Cells and Gene Editing.
Fasciculation
[An MRI study of hereditary spinocerebellar degenerations]
Fatty Liver
Alteration of Hepatic Gene Expression along with the Inherited Phenotype of Acquired Fatty Liver in Chicken.
Arachidyl amido cholanoic acid improves liver glucose and lipid homeostasis in nonalcoholic steatohepatitis via AMPK and mTOR regulation.
BTG1 ameliorates liver steatosis by decreasing stearoyl-CoA desaturase 1 (SCD1) abundance and altering hepatic lipid metabolism.
Carnitine transport by organic cation transporters and systemic carnitine deficiency.
Chronic administration of recombinant IL-6 upregulates lipogenic enzyme expression and aggravates high-fat-diet-induced steatosis in IL-6-deficient mice.
Combined therapy with PPARalpha agonist and L-carnitine rescues lipotoxic cardiomyopathy due to systemic carnitine deficiency.
Dietary polyunsaturated fatty acids mediate the inverse association of stearoyl-CoA desaturase activity with the risk of fatty liver in dyslipidaemic individuals.
Effect of skin-capsular distance on controlled attenuation parameter for diagnosing liver steatosis in patients with nonalcoholic fatty liver disease.
Emerging therapies for the treatment of nonalcoholic steatohepatitis: A systematic review.
Evaluation of various biomarkers as potential mediators of the association between ?5 desaturase, ?6 desaturase, and stearoyl-CoA desaturase activity and incident type 2 diabetes in the European Prospective Investigation into Cancer and Nutrition-Potsdam Study.
Fatty Acid Bile Acid Conjugate Inhibits Hepatic Stearoyl Coenzyme A Desaturase and Is Non-atherogenic.
Fatty Acid Desaturase Involvement in Non-Alcoholic Fatty Liver Disease Rat Models: Oxidative Stress Versus Metalloproteinases.
Fatty Liver Is Associated with Transcriptional Downregulation of Stearoyl-CoA Desaturase and Impaired Protein Dimerization.
Geniposide and Chlorogenic Acid Combination Improves Non-Alcoholic Fatty Liver Disease Involving the Potent Suppression of Elevated Hepatic SCD-1.
Germinated barley downregulates hepatic stearoyl-CoA desaturase-1 enzyme gene expression in a hepatic steatohepatitis rat model.
Hepatic stearoyl-CoA desaturase (SCD)-1 activity and diacylglycerol but not ceramide concentrations are increased in the nonalcoholic human fatty liver.
Hepatocyte-specific deletion of BAP31 promotes SREBP1C activation, promotes hepatic lipid accumulation, and worsens IR in mice.
Kynurenine-Induced Aryl Hydrocarbon Receptor Signaling in Mice Causes Body Mass Gain, Liver Steatosis, and Hyperglycemia.
Lactobacillus Strains Alleviated Hyperlipidemia and Liver Steatosis in Aging Rats via Activation of AMPK.
Low hepatic stearoyl-CoA desaturase 1 activity is associated with fatty liver and insulin resistance in obese humans.
miR-192-5p regulates lipid synthesis in non-alcoholic fatty liver disease through SCD-1.
Molecular and physiological evidence for multifunctionality of carnitine/organic cation transporter OCTN2.
Novel Lipid Long Intervening Noncoding RNA, Oligodendrocyte Maturation-Associated Long Intergenic Noncoding RNA, Regulates the Liver Steatosis Gene Stearoyl-Coenzyme A Desaturase As an Enhancer RNA.
Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter.
Rapid changes in liver lipid composition and pancreatic islet K+ handling and secretory behaviour provoked by the intravenous administration of a medium-chain triglyceride: fish oil emulsion to long-chain polyunsaturated omega3 fatty acid-depleted rats.
Recent advances on stearoyl-CoA desaturase regulation in fatty liver diseases.
Reduced adiposity and liver steatosis by stearoyl-CoA desaturase deficiency are independent of peroxisome proliferator-activated receptor-alpha.
Role of hepatic desaturases in obesity-related metabolic disorders.
Serum fatty acid composition and insulin resistance are independently associated with liver fat markers in elderly men.
Stearoyl-CoA desaturase and tumorigenesis.
Stearoyl-CoA desaturase as a new drug target for obesity treatment.
Stearoyl-CoA desaturase, a short-lived protein of endoplasmic reticulum with multiple control mechanisms.
Sudden cardiac death following liver transplantation: Incidence, trends and risk predictors.
Vitamin A deficiency increases the oleic acid (C18:1) levels in the kidney of high fructose diet-fed rats.
[6]-gingerol dampens hepatic steatosis and inflammation in experimental nonalcoholic steatohepatitis.
[Research progress of stearoyl-CoA desaturase-1 on obesity and non-alcoholic fatty liver disease Abstract].
Fetal Death
Acceptability of In Utero Hematopoietic Cell Transplantation for Sickle Cell Disease.
Outcome of pregnancies among women with sickle cell disease.
Outcome of pregnancies complicated by sickle cell and sickle-C hemoglobinopathies.
Pregnancy and sickle cell disease: A review of the current literature.
Selective prophylactic transfusion in sickle cell disease.
Sickle cell disease and pregnancy outcomes: population-based study on 8.8 million births.
Sickle cell disease and pregnancy outcomes: women of African descent.
Fetal Growth Retardation
Outcome of Pregnancy in Saudi Women with Sickle Cell Disease Attending the Tertiary Care University Hospital in Eastern Province of Saudi Arabia.
Perinatal implications of sickle cell disease.
Pregnancy outcomes in women with sickle-cell disease in low and high income countries: a systematic review and meta-analysis.
Selective prophylactic transfusion in sickle cell disease.
Sickle cell anemia/sickle cell disease and pregnancy outcomes among ethnic tribes in India: an integrative mini-review.
Sickle cell disease and pregnancy outcomes: population-based study on 8.8 million births.
Third-trimester erythrocytapheresis in pregnant patients with sickle cell disease.
Focal Infection
Community-acquired Salmonella bacteraemia in patients with sickle-cell disease 1969-2008: A single centre study.
Folic Acid Deficiency
Effects of a Low FODMAP Diet and Specific Carbohydrate Diet on Symptoms and Nutritional Adequacy of Patients with Irritable Bowel Syndrome: Preliminary Results of a Single-blinded Randomized Trial.
Foramen Ovale, Patent
Patent foramen ovale in patients with sickle cell disease and stroke: case presentations and review of the literature.
Friedreich Ataxia
Cognitive impairment in spinocerebellar degeneration.
[Brain stem auditory evoked potentials in spinocerebellar degeneration]
[Spinocerebellar degeneration in Japan--the feature from an epidemiological study]
Gait Disorders, Neurologic
Clinical and MRI Differences Between Patients With Subacute Combined Degeneration of the Spinal Cord Related vs. Unrelated to Recreational Nitrous Oxide Use: A Retrospective Study.
Gallbladder Diseases
Laparoscopic cholecystectomy in adults with sickle cell disease.
Gallstones
Association between clinical outcomes and metformin use in adults with sickle cell disease and diabetes mellitus.
Laparoscopic cholecystectomy for cholelithiasis in children with sickle cell disease.
Laparoscopic cholecystectomy in 427 adults with sickle cell disease: a single-center experience.
Laparoscopic cholecystectomy in adult patients with sickle cell disease.
Multiple primary choledocholithiasis in sickle cell disease.
Should cholecystectomy be performed concomitantly with splenectomy in children with sickle-cell disease?
Sickle cell disease subphenotypes in patients from southwestern province of saudi arabia.
Sonographic Evaluation of Some Abdominal Organs in Sickle Cell Disease Patients in a Tertiary Health Institution in Northeastern Nigeria.
Splenic complications of the sickling syndromes and the role of splenectomy.
Surgery in sickle cell disease.
Treatment of cholelithiasis in children with sickle cell disease.
UGT1A1 promoter polymorphism associated with serum bilirubin level in Saudi patients with sickle cell disease.
Gastroenteritis
Infections and sickle cell disease in Eastern Saudi Arabian children.
Gastrointestinal Diseases
Subacute combined degeneration of the spinal cord is associated with tripterygium glycoside tablet usage.
GATA2 Deficiency
Fertility preservation before hematopoetic stem cell transplantation: a case series of women with GATA binding protein 2 deficiency, dedicator of cytokinesis 8 deficiency, and sickle cell disease.
Genetic Diseases, Inborn
"You Just Have to Live With It": Coping With Sickle Cell Disease in Jamaica.
'The white blood cell always eat the red': how Jamaicans with sickle cell disease understand their illness.
A review of the literature on the multiple dimensions of chronic pain in adults with sickle cell disease.
Carnitine transport by organic cation transporters and systemic carnitine deficiency.
Classic and Novel Biomarkers as Potential Predictors of Ventricular Arrhythmias and Sudden Cardiac Death.
Diverse requirements for Notch signalling in mammals.
Epidemiology of sickle cell disease in Saudi Arabia.
Genome editing and stem cell therapy pave the path for new treatment of sickle-cell disease.
Health-related quality of life of adolescents with sickle cell disease in sub-Saharan Africa: a cross-sectional study.
Hematopoietic cell transplantation for thalassemia and sickle cell disease: past, present and future.
Hypertrophic cardiomyopathy--state of the art in 2007.
In vitro and in vivo anti-angiogenic effects of hydroxyurea.
Influence of gender norms in relation to child's quality of care: follow-up of families of children with SCD identified through NBS in Tanzania.
Neonatal screening for sickle cell disease in France.
Patient Outcomes From a Specialized Inherited Arrhythmia Clinic.
Recent insights on the medicinal chemistry of sickle cell disease.
Reduced cholesterol levels in African-American adults with sickle cell disease.
Renal abnormalities in sickle cell disease.
Seamless correction of the sickle cell disease mutation of the HBB gene in human induced pluripotent stem cells using TALENs.
Students' knowledge on sickle cell disease in Kisangani, Democratic Republic of the Congo.
Subacute combined degeneration of the spinal cord is associated with tripterygium glycoside tablet usage.
Technical in-depth comparison of two massive parallel DNA-sequencing methods for formalin-fixed paraffin-embedded tissue from victims of sudden cardiac death.
Transition and sickle cell disease.
Use of genetic testing to identify sudden cardiac death syndromes.
Glaucoma
Recurrent orbital bone sub-periosteal hematoma in sickle cell disease: a case study.
The Occurrence and Proposed Significance of Schnabel Cavernous Degeneration in Uveal Melanoma.
Glioblastoma
Expression of SCD and FADS2 Is Lower in the Necrotic Core and Growing Tumor Area than in the Peritumoral Area of Glioblastoma Multiforme.
Mechanisms of stearoyl CoA desaturase inhibitor sensitivity and acquired resistance in cancer.
Stearoyl CoA Desaturase Is Essential for Regulation of Endoplasmic Reticulum Homeostasis and Tumor Growth in Glioblastoma Cancer Stem Cells.
Glioma
Antipsychotic drugs activate SREBP-regulated expression of lipid biosynthetic genes in cultured human glioma cells: a novel mechanism of action?
IDH1 mutations induce organelle defects via dysregulated phospholipids.
SREBP maintains lipid biosynthesis and viability of cancer cells under lipid- and oxygen-deprived conditions and defines a gene signature associated with poor survival in glioblastoma multiforme.
Glomerulonephritis
Atypical presentation of acute post-infectious glomerulonephritis in patients with sickle cell disease: report of two cases.
Subacute combined degeneration of the spinal cord is associated with tripterygium glycoside tablet usage.
Glucose Intolerance
Diabetes, glucose tolerance, and the risk of sudden cardiac death.
Exposure to high fructose corn syrup during adolescence in the mouse alters hepatic metabolism and the microbiome in a sex-specific manner.
Platelet hyperaggregability in high-fat fed rats: A role for intraplatelet reactive-oxygen species production.
Sudden cardiac death in patients with diabetes.
The dual-specificity phosphatase 2 (DUSP2) does not regulate obesity-associated inflammation or insulin resistance in mice.
glucose-6-phosphate dehydrogenase (nadp+) deficiency
Clinical significance of glucose-6-phosphate dehydrogenase deficiency in Nigerian patients with sickle cell disease.
Comorbidity of Glucose-6-Phosphate Dehydrogenase Deficiency and Sickle Cell Disease Exert Significant Effect on RBC Indices.
Genetic modifiers of severity in sickle cell disease.
Glucose-6-phosphate dehydrogenase deficiency and sickle cell disease in Burkina Faso.
Thalassaemia and glucose-6-phosphate dehydrogenase deficiency in sickle-cell disorder patients in Taiz, Yemen.
The clinical impact of glucose-6-phosphate dehydrogenase deficiency in patients with sickle cell disease.
The CYB5R3c.350C>G and G6PD A alleles modify severity of anemia in malaria and sickle cell disease.
Updated Worldwide Epidemiology of Inherited Erythrocyte Disorders.
Varied Age of First Presentation of Sickle Cell Disease: Case Presentations and Review.
[Neonatal screening of hemoglobinopathies and G6PD deficiency in Catalonia (Spain). Molecular study of sickle cell disease associated with alpha thalassemia and G6PD deficiency]
Glucosephosphate Dehydrogenase Deficiency
Comorbidity of Glucose-6-Phosphate Dehydrogenase Deficiency and Sickle Cell Disease Exert Significant Effect on RBC Indices.
Genetic modifiers of severity in sickle cell disease.
Thalassaemia and glucose-6-phosphate dehydrogenase deficiency in sickle-cell disorder patients in Taiz, Yemen.
The clinical impact of glucose-6-phosphate dehydrogenase deficiency in patients with sickle cell disease.
The CYB5R3c.350C>G and G6PD A alleles modify severity of anemia in malaria and sickle cell disease.
Updated Worldwide Epidemiology of Inherited Erythrocyte Disorders.
Varied Age of First Presentation of Sickle Cell Disease: Case Presentations and Review.
[Neonatal screening of hemoglobinopathies and G6PD deficiency in Catalonia (Spain). Molecular study of sickle cell disease associated with alpha thalassemia and G6PD deficiency]
Glycogen Storage Disease Type IIb
Sudden cardiac death in neuromuscular disorders.
Graft vs Host Disease
A cure for murine sickle cell disease through stable mixed chimerism and tolerance induction after nonmyeloablative conditioning and major histocompatibility complex-mismatched bone marrow transplantation.
Allogeneic hematopoietic stem cell transplantation from sibling and unrelated donors in pediatric patients with sickle cell disease-A single center experience.
Allogeneic stem cell transplantation for sickle cell disease.
Alternative donor hematopoietic stem cell transplantation for sickle cell disease in Europe.
Alternative donor: ?ß/CD19 T-cell-depleted haploidentical hematopoietic stem cell transplantation for sickle cell disease.
Curative options for sickle cell disease: haploidentical stem cell transplantation or gene therapy?
Status quo of allogeneic stem cell transplantation for patients with sickle cell disease using matched unrelated donors.
Granuloma
Granulomas at initial diagnosis of Crohn's disease signal a poor outcome.
Graves Disease
Association of BTG2, CYR61, ZFP36, and SCD gene polymorphisms with Graves' disease and ophthalmopathy.
Guillain-Barre Syndrome
Subacute combined degeneration of the spinal cord with concomitant autoimmune disease: report of 2 cases.
Haemophilus Infections
Conjugate Haemophilus influenzae type b vaccines for sickle cell disease.
Hand-Foot Syndrome
Microfluidics in Sickle Cell Disease Research: State of the Art and a Perspective Beyond the Flow Problem.
Head and Neck Neoplasms
Chronic exposure to chewing tobacco selects for overexpression of stearoyl-CoA desaturase in normal oral keratinocytes.
Head Injuries, Closed
Temporal bone fracture causing superior semicircular canal dehiscence.
Headache Disorders
Headache symptoms in pediatric sickle cell patients.
Headache Disorders, Primary
Headache and Facial Pain in Sickle Cell Disease.
Headache Disorders, Secondary
Headache and Facial Pain in Sickle Cell Disease.
Hearing Loss
Assessment of the effects of superior canal dehiscence location and size on intracochlear sound pressures.
Audiologic, cVEMP, and Radiologic Progression in Superior Canal Dehiscence Syndrome.
Auditory-evoked response analysis in Brazilian patients with sickle cell disease.
Characterization of Sensorineural Hearing Loss in Adult Patients With Sickle Cell Disease: A Systematic Review and Meta-analysis.
Childhood Hearing Loss in Patients With Sickle Cell Disease in the United States.
Complete recovery following sudden sensorineural hearing loss in a patient with sickle cell disease.
Development of conductive hearing loss due to posterior semicircular canal dehiscence.
Hearing loss among adults with sickle cell disease in an endemic region: a prospective case-control study.
hearing loss in Angolan children with sickle-cell disease.
Hearing loss in children with sickle cell disease: A prospective French cohort study.
Influence of Semicircular Canal Dehiscence on Cochlear Implant Outcome.
Insights into elevated distortion product otoacoustic emissions in sickle cell disease: Comparisons of hydroxyurea-treated and non-treated young children.
Measurements of human middle- and inner-ear mechanics with dehiscence of the superior semicircular canal.
Prevalence and nature of hearing loss in a cohort of children with sickle cell disease.
Prevalence of Sensorineural Hearing Loss in Pediatric Patients with Sickle Cell Disease: A Meta-analysis.
Sensorineural hearing loss in children with sickle cell disease.
Superior Canal Dehiscence Similarly Affects Cochlear Pressures in Temporal Bones and Audiograms in Patients.
Surgical treatments for a case of superior canal dehiscence syndrome associated with patulous Eustachian tube.
The emergence and prevalence of hearing loss in children with homozygous sickle cell disease.
The evaluation of auditory function in homozygous sickle cell disease.
The Profiles of Students With Significant Cognitive Disabilities and Known Hearing Loss.
Three-Dimensional Printed Prosthesis for Repair of Superior Canal Dehiscence.
Hearing Loss, Bilateral
hearing loss in Angolan children with sickle-cell disease.
Hearing Loss, Conductive
A Case Series of Patients With Concurrent Otosclerosis and Superior Semicircular Canal Dehiscence.
A superior semicircular canal dehiscence-induced air-bone gap in chinchilla.
Development of conductive hearing loss due to posterior semicircular canal dehiscence.
Prospective radiological study concerning a series of patients suffering from conductive or mixed hearing loss due to superior semicircular canal dehiscence.
The effect of superior canal dehiscence on cochlear potential in response to air-conducted stimuli in chinchilla.
Vestibular-evoked myogenic potentials in the diagnosis of superior canal dehiscence syndrome.
Hearing Loss, Mixed Conductive-Sensorineural
Prospective radiological study concerning a series of patients suffering from conductive or mixed hearing loss due to superior semicircular canal dehiscence.
Hearing Loss, Sensorineural
Prevalence and nature of hearing loss in a cohort of children with sickle cell disease.
Prevalence of Jervell-Lange Nielsen syndrome in children with congenital bilateral sensorineural hearing loss.
Sensorineural hearing loss in Nigerian children with sickle cell disease.
Utility of cVEMPs in bilateral superior canal dehiscence syndrome.
Heart Arrest
A common SCN5A variant is associated with PR interval and atrial fibrillation among African Americans.
A validation study of the European Society of Cardiology guidelines for risk stratification of sudden cardiac death in childhood hypertrophic cardiomyopathy.
Amiodarone versus other pharmacological interventions for prevention of sudden cardiac death.
Arrhythmic events in Brugada syndrome patients induced by fever.
Arrhythmogenic Right Ventricular Cardiomyopathy: A Review of Living and Deceased Probands.
Arrhythmogenic Right Ventricular Cardiomyopathy: Risk Stratification and Indications for Defibrillator Therapy.
Arrhythmogenic ventricular cardiomyopathy: A paradigm shift from right to biventricular disease.
Cardiac arrest and sudden cardiac death registries: a systematic review of global coverage.
Cardiac Function and Sudden Cardiac Death in Heart Failure With Preserved Ejection Fraction (from the TOPCAT Trial).
Cardiovascular genomics and sudden cardiac death in the young.
Catheter Ablation for Brugada Syndrome.
Chronic obstructive pulmonary disease and sudden cardiac death: A systematic review.
Clinical use of magnetic resonance imaging for the diagnosis of acute myocardial infarction in the survivors of cardiac arrest.
Clinical Use of Magnetic Resonance Imaging for the Diagnosis of Acute Myocardial Infarction in the Survivors of Cardiac Arrest.
Cold spells and ischaemic sudden cardiac death: effect modification by prior diagnosis of ischaemic heart disease and cardioprotective medication.
Comparison of Features of Fatal Versus Nonfatal Cardiac Arrest in Patients With Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy.
CPR in medical schools: learning by teaching BLS to sudden cardiac death survivors--a promising strategy for medical students?
Defibrillation for Ventricular Fibrillation: A Shocking Update.
Development of a Novel Risk Prediction Model for Sudden Cardiac Death in Childhood Hypertrophic Cardiomyopathy (HCM Risk-Kids).
Epidemiology and stratification of risk for sudden cardiac death.
Hypertrophic Cardiomyopathy-Related Sudden Cardiac Death in Young People in Ontario.
Implantable cardioverter defibrillator for prevention of sudden cardiac death in patients with ventricular tachycardia and ventricular fibrillation: ICD therapy in sudden cardiac death.
Implantable Cardioverter Defibrillator Therapy in Patients with Acute Decompensated Heart Failure with Reduced Ejection Fraction: An Observation from the KCHF Registry.
Implantable cardioverter defibrillators. Prophylactic use: an evidence-based analysis.
Implantable cardioverter-defibrillators in children.
Implantable device therapy.
Improvement in sudden cardiac death risk prediction by the enhanced American College of Cardiology/American Heart Association strategy in Chinese patients with hypertrophic cardiomyopathy.
Incidence of sudden cardiac death in Germany: results from an emergency medical service registry in Lower Saxony.
Life expectancy gains and cost-effectiveness of implantable cardioverter/defibrillators for the primary prevention of sudden cardiac death in patients with hypertrophic cardiomyopathy.
Mechanisms of sudden cardiac death.
Mitral Valve Prolapse and Sudden Cardiac Death: A Systematic Review.
Modes of death and clinical outcomes in adult patients with hypertrophic cardiomyopathy in Thailand.
NOS1AP Polymorphisms Modify QTc Interval Duration But Not Cardiac Arrest Risk in Hypertrophic Cardiomyopathy.
Novel Variants in TECRL Cause Catecholaminergic Polymorphic Ventricular Tachycardia.
Paced ventricular electrogram fractionation predicts sudden cardiac death in hypertrophic cardiomyopathy.
Pathology of the myocardium and the conduction system in sudden coronary death.
Predictors of Long-Term Outcome in Children with Hypertrophic Cardiomyopathy.
Prevention of Sudden Cardiac Death in Children and Young Adults.
Prognostic Role of Late Gadolinium Enhancement in Patients With Hypertrophic Cardiomyopathy and Low-to-Intermediate Sudden Cardiac Death Risk Score.
Prognostic value of electrocardiographic time intervals and QT rate dependence in hypertrophic cardiomyopathy.
Public health impact of daily life triggers of sudden cardiac death: A systematic review and comparative risk assessment.
QT interval dispersion in healthy subjects and survivors of sudden cardiac death: circadian variation in a twenty-four-hour assessment.
Rationale and design of the Pan-African Sudden Cardiac Death survey: the Pan-African SCD study.
Relationship between impaired repolarization parameters and poor cardiovascular clinical outcomes in patients with potentially serious coronary artery anomalies.
Risk factors for sudden cardiac death in childhood hypertrophic cardiomyopathy: A systematic review and meta-analysis.
Risk of Death in Long-Term Follow-Up of Patients With Apical Hypertrophic Cardiomyopathy.
Risk stratification for sudden cardiac death in hypertrophic cardiomyopathy: systematic review of clinical risk markers.
Risk Stratification in Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia Without an Implantable Cardioverter-Defibrillator.
Role of drugs and devices in patients at risk of sudden cardiac death.
Sex Differences in Electrophysiology, Ventricular Tachyarrhythmia, Cardiac Arrest and Sudden Cardiac Death Following Acute Myocardial Infarction.
Sudden Cardiac and Noncardiac Death in Sports: Epidemiology, Causes, Pathogenesis, and Prevention.
Sudden cardiac death and chronic kidney disease: From pathophysiology to treatment strategies.
Sudden Cardiac Death and Post Cardiac Arrest Syndrome. An Overview.
Sudden cardiac death during physical exercise: Characteristics of victims and autopsy findings.
Sudden cardiac death in post myocardial infarction patients.
Sudden cardiac death: A reappraisal.
Temporal distribution of arrhythmic events in chronic kidney disease: Highest incidence in the long interdialytic period.
The Efficacy of Beta-Blockers in Patients With Long QT Syndrome 1-3 According to Individuals' Gender, Age, and QTc Intervals: A Network Meta-analysis.
The MUSTT study: evaluating testing and treatment.
The role of implantable cardioverter defibrillators in non VT/VF sudden deaths.
Usefulness of Electrocardiographic Patterns at Presentation to Predict Long-term Risk of Cardiac Death in Patients With Hypertrophic Cardiomyopathy.
Ventricular arrhythmia following alcohol septal ablation for obstructive hypertrophic cardiomyopathy.
[Relationship between arrhythmia profile, left ventricular function and sudden death in the post-infarct period of patients resuscitated from heart arrest]
{beta}2-Adrenergic Receptor Genetic Variants and Risk of Sudden Cardiac Death.
Heart Block
Determinants of Sudden Cardiac Death in Adult Patients With Eisenmenger Syndrome.
Mechanisms of sudden cardiac death.
Heart Defects, Congenital
Identification of patients at risk of sudden cardiac death in congenital heart disease: The PRospEctiVE study on implaNTable cardIOverter defibrillator therapy and suddeN cardiac death in Adults with Congenital Heart Disease (PREVENTION-ACHD).
Impact of different selection policies on subcutaneous ICD implants and therapies.
Implantable cardioverter-defibrillator therapy in adult patients with tetralogy of Fallot.
Implantable defibrillators: from the adult cardiac to the grown up congenital heart disease patient.
Physical Activity Recommendations for Patients With Electrophysiologic and Structural Congenital Heart Disease: A Survey of Canadian Health Care Providers.
PREVENTION-ACHD: PRospEctiVE study on implaNTable cardioverter-defibrillator therapy and suddeN cardiac death in Adults with Congenital Heart Disease; Rationale and Design.
Sickle cell disease and complex congenital cardiac surgery: a case report and review of the pathophysiology and perioperative management.
Spondylocostal dysostosis with tetralogy of Fallot and herniation of the spleen through the diaphragm.
Sudden cardiac death and late arrhythmias after the Fontan operation.
Sudden cardiac death in pediatrics.
Sudden cardiac death in young people with apparently normal heart.
Sudden cardiac death.
Surgical therapy for sudden cardiac death in children.
Use of genetic testing to identify sudden cardiac death syndromes.
[Sudden cardiac death in women].
Heart Diseases
A novel mutation of dipeptidyl aminopeptidase-like protein-6 in a family with suspicious idiopathic ventricular fibrillation.
Adherence to a low-risk, healthy lifestyle and risk of sudden cardiac death among women.
Advances in the prevention of sudden cardiac death in the young.
All-Cause Mortality and Incidence of Major Adverse Cardiac Events in Sickle Cell Nephropathy: A Comparative Study.
Association between circadian Holter ECG changes and sudden cardiac death in patients with Chagas heart disease.
Asymmetry of Hippocampus and Amygdala Defect in Subjective Cognitive Decline Among the Community Dwelling Chinese.
Autoantibodies for Cardiac Channels and Sudden Cardiac Death and its Relationship to Autoimmune Disorders.
Beat-to-beat repolarization lability identifies patients at risk for sudden cardiac death.
Blood alcohol levels in Finnish victims of non-ischaemic sudden cardiac death.
Brain natriuretic peptide for the prediction of sudden cardiac death and ventricular arrhythmias: a meta-analysis.
Cardiac arrhythmias and sudden death in infancy: implication for the medicolegal investigation.
Cardiac issues in the young athlete.
Cardiac magnetic resonance characteristics in young survivors of aborted sudden cardiac death.
Cardiac Magnetic Resonance in Primary Prevention of Sudden Cardiac Death.
Cardiovascular risk factors differently affect the survival of patients undergoing manual or mechanical resuscitation.
Catecholaminergic polymorphic ventricular tachycardia, an update.
Catheter ablation to prevent sudden cardiac death.
Causes of nonischemic sudden cardiac death in the current era.
Characteristics of subjects with alcoholic cardiomyopathy and sudden cardiac death.
Childhood stroke in Eastern Province, KSA: pattern, risk factors, diagnosis and outcome.
Clinical management of ventricular tachycardia.
Clinical Predictive Value of Cystatin C in Pediatric Sickle Cell Disease: A Marker of Disease Severity and Subclinical Cardiovascular Dysfunction.
Clinical Usefulness of Wearable Cardioverter Defibrillator (WCD) and Current Understanding of Its Clinical Indication in Japan.
Clustering of end-organ disease and earlier mortality in adults with sickle cell disease: A retrospective-prospective cohort study.
Comorbid Chronic Conditions Among Older Adults with Subjective Cognitive Decline, United States, 2015-2017.
Comparison of family history of sudden cardiac death in nonischemic and ischemic heart disease.
Coronary atherosclerosis in unheralded sudden coronary death under age 50: histo-pathologic comparison with 'healthy' subjects dying out of hospital.
Diabetes, glucose tolerance, and the risk of sudden cardiac death.
Diagnostic findings and follow-up outcomes in relatives to young non-autopsied sudden death victims.
Diagnostic yield in victims of sudden cardiac death and their relatives.
Differential Methylation in the GSTT1 Regulatory Region in Sudden Unexplained Death and Sudden Unexpected Death in Epilepsy.
Do 'pathologic' cardiac murmurs in adolescents identify structural heart disease? An evaluation of 15 141 active adolescents for conditions that put them at risk of sudden cardiac death.
Early Repolarization Disease.
Echocardiography in Athletes in Primary Prevention of Sudden Death.
Effect of Obstructive Sleep Apnea on QT Dispersion: A Potential Mechanism of Sudden Cardiac Death.
Electrocardiogram as a predictor of sudden cardiac death in middle-aged subjects without a known cardiac disease.
Electrocardiogram Screening for Disorders That Cause Sudden Cardiac Death in Asymptomatic Children: A Meta-analysis.
Electrocardiograms in athletes: interpretation and diagnostic accuracy.
Electrocardiographic predictors of mortality and sudden cardiac death in patients with end stage renal disease on hemodialysis.
Epidemiology and stratification of risk for sudden cardiac death.
Exercise Related Sudden Cardiac Death: The Experience of a Tertiary Referral Pathology Centre in the United Kingdom.
Fatty acid desaturation index in human plasma: comparison of different analytical methodologies for the evaluation of diet effects.
Feasibility of entirely subcutaneous ICD™ systems in patients with coronary artery disease.
Fish and n-3 fatty acids for the prevention of fatal coronary heart disease and sudden cardiac death.
Fragmented ECG as a risk marker in cardiovascular diseases.
Fragmented QRS and other depolarization abnormalities as a predictor of mortality and sudden cardiac death.
Future developments in implantable cardioverter defibrillators: the optimal device.
Gender differences in sudden cardiac death in the young-a nationwide study.
Genetic Variants Associated With Unexplained Sudden Cardiac Death in Adult White and African American Individuals.
Genetics of sudden cardiac death caused by ventricular arrhythmias.
Genomics in sudden cardiac death.
Holter monitoring in the prognosis of sudden cardiac death.
Identification of genes associated with sudden cardiac death: a network- and pathway-based approach.
Implantable cardioverter defibrillator therapy.
Implantable cardioverter defibrillator use for primary prevention in ischaemic and non-ischaemic heart disease-indications in the post-DANISH trial era: results of the European Heart Rhythm Association survey.
Implantable cardioverter defibrillators. Prophylactic use: an evidence-based analysis.
Incidence and aetiology of sudden cardiac death in young athletes: an international perspective.
Increased left main coronary artery dimensions in children with sickle cell disease.
Influence of functional polymorphism in MIF promoter on sudden cardiac death in Chinese populations.
Insights into sudden cardiac death: exploring the potential relevance of non-diagnostic autopsy findings.
Interleukin-18 promoter polymorphism associates with the occurrence of sudden cardiac death among Caucasian males: the Helsinki Sudden Death Study.
International criteria for electrocardiographic interpretation in athletes.
International recommendations for electrocardiographic interpretation in athletes.
International Recommendations for Electrocardiographic Interpretation in Athletes.
Ischemic Heart Disease Related Sudden Cardiac Death in Autopsied Cases: An Egyptian perspective.
Lethal immunoglobulins: Autoantibodies and sudden cardiac death.
Long-term follow-up after atrioventricular nodal ablation and pacing: low incidence of sudden cardiac death.
Malignant Dysrhythmias - Brugada Type 1 Pattern Formation in the Presence of Fever.
Management of arrhythmias in ischemic heart disease. The role of beta blockers.
Massively Parallel Sequencing of Genes Implicated in Heritable Cardiac Disorders: A Strategy for a Small Diagnostic Laboratory.
Molecular autopsy in victims of inherited arrhythmias.
Molecular autopsy of sudden unexplained deaths reveals genetic predispositions for cardiac diseases among young forensic cases.
Monomorphic Ventricular Arrhythmias in Athletes.
Mortality and appropriate and inappropriate therapy in patients with ischaemic heart disease and implanted cardioverter-defibrillators for primary prevention: data from the Danish ICD Register.
Non-arrhythmic causes of sudden death: A comprehensive review.
Outcome of clinical management in relatives of sudden cardiac death victims.
Outcomes of Catheter Ablation in Arrhythmogenic Right Ventricular Cardiomyopathy Without Background Implantable Cardioverter Defibrillator Therapy: A Multicenter International Ventricular Tachycardia Registry.
Outcomes of patients admitted with ventricular arrhythmias and sudden cardiac death in the United States.
Pacemaker implantation in a patient with brugada and sick sinus syndrome.
Pathophysiology and prevention of sudden cardiac death.
Postmortem mRNA expression patterns in left ventricular myocardial tissues and their implications for forensic diagnosis of sudden cardiac death.
Pre-participation screening for the prevention of sudden cardiac death in athletes.
Prediction of ventricular tachyarrhythmias by intracardiac repolarization variability analysis.
Predictors of appropriate ICD therapy in Japanese patients with structural heart diseases: A major role of prior sustained ventricular tachycardia in secondary prevention.
Predictors of sudden cardiac death.
Premature ventricular beats in the athlete: management considerations.
Preparticipation screening and preparticipation forms.
Preparticipation screening and prevention of sudden cardiac death in athletes: Implications for primary care.
Preventing tomorrow's sudden cardiac death today: part I: Current data on risk stratification for sudden cardiac death.
Prevention of stroke in sickle cell anemia.
Prevention of sudden cardiac death by the implantable cardioverter-defibrillator.
Primary prevention of sudden cardiac death.
Problems in forensic cardiovascular pathology.
Prospective study of sudden cardiac death among women in the United States.
Rationale and design of the CAREFUL study : The yield of CARdiogenetic scrEening in First degree relatives of sudden cardiac and UnexpLained death victims <45 years.
Relations among renal function, risk of sudden cardiac death, and benefit of the implanted cardiac defibrillator in patients with ischemic left ventricular dysfunction.
Relevance of molecular testing in patients with a family history of sudden death.
Retrospective Analysis of Sudden Cardiac Deaths in a 10-Year Autopsy Series in the City of Isparta in Turkey.
Right Ventricular Dysfunction and Long-Term Risk of Sudden Cardiac Death in Patients With and Without Severe Left Ventricular Dysfunction.
Risk factor assessment: defining populations and individuals at risk.
Risk markers of sudden cardiac death in standard 12-lead electrocardiograms.
Risk stratification and primary prevention of sudden cardiac death: sudden death prevention.
Risk stratification for sudden cardiac death: current status and challenges for the future.
Role of copy number variants in sudden cardiac death and related diseases: genetic analysis and translation into clinical practice.
Role of pharmacotherapy in cardiac ion channelopathies.
Screening young athletes for prevention of sudden cardiac death: Practical recommendations for sports physicians.
Serum apelin as a novel non-invasive marker for subclinical cardiopulmonary complications in children and adolescents with sickle cell disease.
Significance of deep T-wave inversions in asymptomatic athletes with normal cardiovascular examinations: practical solutions for managing the diagnostic conundrum.
Sleep Apnea and Sudden Cardiac Death.
Small coronary vessel disease and sudden coronary death.
Soluble CD74 Reroutes MIF/CXCR4/AKT-Mediated Survival of Cardiac Myofibroblasts to Necroptosis.
Strategy for clinical evaluation and screening of sudden cardiac death relatives.
Structural pathways and prevention of heart failure and sudden death.
Sudden cardiac death and chronic kidney disease: From pathophysiology to treatment strategies.
Sudden cardiac death and the use of implantable cardioverter-defibrillators in pediatric patients. The Pediatric Electrophysiology Society.
Sudden cardiac death during physical exercise: Characteristics of victims and autopsy findings.
Sudden cardiac death from structural heart diseases in adults: imaging findings with cardiovascular computed tomography and magnetic resonance.
Sudden cardiac death in adults with congenital heart disease: does QRS-complex fragmentation discriminate in structurally abnormal hearts?
Sudden Cardiac Death in Athletes: Still Much to Learn.
Sudden cardiac death in athletes: the Lausanne Recommendations.
Sudden cardiac death in children and young adults without structural heart disease: a comprehensive review.
Sudden cardiac death in China.
Sudden cardiac death in dialysis patients: different causes and management strategies.
Sudden cardiac death in infants, children, and adolescents.
Sudden Cardiac Death in Ischemic Heart Disease: From Imaging Arrhythmogenic Substrate to Guiding Therapies.
Sudden cardiac death in Long QT syndrome (LQTS), Brugada syndrome, and catecholaminergic polymorphic ventricular tachycardia (CPVT).
Sudden cardiac death in the United States, 1989 to 1998.
Sudden Cardiac Death in the Young: A Strategy for Prevention by Targeted Evaluation.
Sudden cardiac death in the young: how can disease recognition and prevention in family members be improved?
Sudden cardiac death in the young: the molecular autopsy and a practical approach to surviving relatives.
Sudden cardiac death in women.
Sudden Cardiac Death in Women.
Sudden cardiac death in young people with apparently normal heart.
Sudden Cardiac Death not Related to Coronary Atherosclerosis.
Sudden cardiac death: a nationwide cohort study among the young.
Sudden coronary death in middle age and characteristics of its victims in Finland. A prospective population study.
Sudden death related cardiomyopathies - Arrhythmogenic right ventricular cardiomyopathy, arrhythmogenic cardiomyopathy, and exercise-induced cardiomyopathy.
Sudden death. A neurocardiologic phenomenon.
Sustained ventricular tachycardia in structural heart disease.
SVAD: A genetic database curates non-ischemic sudden cardiac death-associated variants.
T-wave alternans and sudden cardiac death.
Targeted molecular genetic testing in young sudden cardiac death victims from Western Denmark.
Temporal trends and sex differences in sudden cardiac death in the Copenhagen City Heart Study.
Temporal trends in coronary heart disease mortality and sudden cardiac death from 1950 to 1999: the Framingham Heart Study.
Temporal trends in sudden cardiac death in Ontario, Canada.
Ten advances defining sudden cardiac death.
The coronary artery calcification severity on postmortem CT could be a clue for the diagnosis of sudden cardiac death.
The diagnosis and management of short QT syndrome.
The Impending Dilemma of Electrocardiogram Screening in Athletic Children.
The interplay between CKD, sudden cardiac death, and ventricular arrhythmias.
The role of genetics in primary ventricular fibrillation, inherited channelopathies and cardiomyopathies.
The spectrum of epidemiology underlying sudden cardiac death.
The worsening of left ventricular hypertrophy is the strongest predictor of sudden cardiac death in haemodialysis patients: a 10 year survey.
Therapy for ventricular arrhythmias in structural heart disease: A multifaceted challenge.
Tools for risk stratification of sudden cardiac death: A review of the literature in different patient populations.
Usefulness of Single Nucleotide Polymorphisms as Predictors of Sudden Cardiac Death.
Utility of electrophysiological studies to predict arrhythmic events.
Ventricular arrhythmia and sudden cardiac death in Fabry disease: a systematic review of risk factors in clinical practice.
Whole genome and transcriptome sequencing of post-mortem cardiac tissues from sudden cardiac death victims identifies a gene regulatory variant in NEXN.
[Antiarrhythmic agents in the prevention of sudden cardiac death]
[Cardiological assessment of surviving family members of sudden cardiac death victims: diagnostic yield].
[Effect of -3 polyunsaturated Fatty acids on predictors of sudden cardiac death in patients with ischemic heart disease and ventricular rhythm disturbances].
[How to reduce the sudden non-traumatic death related to sport risk ?]
[Premature ventricular beats in young athletes: interpretation and diagnostic pathway].
[Sudden cardiac death and automated external defibrillators. Where we are in 2012?].
[Sudden cardiac death due to primary cardiac ion-channel diseases.]
[Sudden cardiac death in athletes and its prevention].
[Sudden cardiac death of incarcerated prisoners: a study of 75 cases].
[Sudden cardiac death: state of the art]
[Sudden cardiac death: toward the identification of susceptibity genes]
[The athletes' ECG and the exercise related sudden cardiac death].
[Worldwide experience with automated external defibrillators : What have we achieved? What else can we expect?].
Heart Failure
12-lead electrocardiogram as a predictor of sudden cardiac death: from epidemiology to clinical practice.
A guide to device selection: cardiac resynchronization therapy alone or in combination with an implantable cardioverter defibrillator.
A Latin American registry of implantable cardioverter defibrillators: the ICD-LABOR study.
A novel LMNA nonsense mutation causes two distinct phenotypes of cardiomyopathy with high risk of sudden cardiac death in a large five-generation family.
Acute effects of angiotensin II receptor blocker on ventricular repolarization alternans in chronic heart failure.
Analysis of T-wave Alternans in ambulatory recordings using the ADTWA index.
Are women worldwide under-treated with regard to cardiac resynchronization and sudden death prevention?
Arrhythmogenic Cardiomyopathy-Current Treatment and Future Options.
Arrhythmogenic right ventricular cardiomyopathy: ECG progression over time and correlation with long-term follow-up.
Association Between Atrial Fibrillation and Sudden Cardiac Death: Pathophysiological and Epidemiological Insights.
Association between Clinical and Doppler Echocardiographic Parameters with Sudden Death in Hemodialysis Patients.
Association Between Depression and Clinical Outcomes in Patients With Hypertrophic Cardiomyopathy.
Association between mitochondrial DNA copy number and sudden cardiac death: findings from the Atherosclerosis Risk in Communities study (ARIC).
Association of prolonged QRS duration with ventricular tachyarrhythmias and sudden cardiac death in the Multicenter Automatic Defibrillator Implantation Trial II (MADIT-II).
Association of vitamin D deficiency with heart failure and sudden cardiac death in a large cross-sectional study of patients referred for coronary angiography.
Atorvastatin therapy may reduce the incidence of sudden cardiac death in patients with advanced chronic heart failure.
Atrial fibrillation and its association with sudden cardiac death.
Atrial fibrillation is associated with sudden cardiac death: a systematic review and meta-analysis.
B-type natruiretic peptide levels stratify the risk for arrhythmia among implantable cardioverter defibrillator patients.
Biventricular pacemaker and defibrillator implantation in patients with chronic heart failure in China.
Cardiac Function and Sudden Cardiac Death in Heart Failure With Preserved Ejection Fraction (from the TOPCAT Trial).
Changes in BNP and QTc for prediction of sudden death in heart failure.
Characteristics of Acute Care Utilization of a Delaware Adult Sickle Cell Disease Patient Population.
Clinical Manifestations and Long-Term Mortality in Lamin A/C Mutation Carriers From a Japanese Multicenter Registry.
Clinical significance of new-onset atrial fibrillation in patients with hypertrophic cardiomyopathy.
Common Variants in TRDN and CALM1 Are Associated with Risk of Sudden Cardiac Death in Chronic Heart Failure Patients in Chinese Han Population.
CRT-Pacemaker Versus CRT-Defibrillator Who Needs Sudden Cardiac Death Protection?
Current challenges in sudden cardiac death prevention.
Deficiency of a novel gene, Yulink, predisposes to heart failure and ventricular arrhythmia.
Determinants of Sudden Cardiac Death in Adult Patients With Eisenmenger Syndrome.
Diagnosis and management of hypertrophic cardiomyopathy.
Dialysis modality-related disparities in sudden cardiac death: hemodialysis versus peritoneal dialysis.
Dissociation of hemodynamic and electrocardiographic indexes of myocardial ischemia in pigs with hibernating myocardium and sudden cardiac death.
Doppler ultrasonographic evaluation of celiac and mesenteric arteries in subjects with sickle cell disease.
Drug Therapy for Ventricular Tachyarrhythmia in Heart Failure.
Dynamic changes in cardiovascular and systemic parameters prior to sudden cardiac death in heart failure with reduced ejection fraction: a PARADIGM-HF analysis.
ECG Quantification of Myocardial Scar and Risk Stratification in MADIT-II.
Echocardiographic Predictors of Sudden Cardiac Death: The Atherosclerosis Risk in Communities Study and Cardiovascular Health Study.
Effects of amiodarone on the circadian pattern of sudden cardiac death (Department of Veterans Affairs Congestive Heart Failure-Survival Trial of Antiarrhythmic Therapy).
Efficacy of cardiac resynchronization therapy in very old patients: the Insync/Insync ICD Italian Registry.
Epidemiology and stratification of risk for sudden cardiac death.
Evidence regarding clinical use of microvolt T-wave alternans.
Fragmented ECG as a risk marker in cardiovascular diseases.
Genomics in sudden cardiac death.
Genomics, heart failure and sudden cardiac death.
Heart rate variability as predictive factor for sudden cardiac death.
Hypertension Is a Risk Factor for Several Types of Heart Disease: Review of Prospective Studies.
Hypertrophic cardiomyopathy with a large apical ventricular aneurysm and mural thrombus.
Identification, clinical manifestation and structural mechanisms of mutations in AMPK associated cardiac glycogen storage disease.
Impact of mineralocorticoid receptor antagonists on the risk of sudden cardiac death in patients with heart failure and left-ventricular systolic dysfunction: an individual patient-level meta-analysis of three randomized-controlled trials.
Impact of statin therapy on all-cause mortality and ICD interventions in heart failure patients - a systematic review.
Implantable cardioverter defibrillators. Prophylactic use: an evidence-based analysis.
Implantable cardioverter-defibrillators for primary prevention of sudden cardiac death in patients with left ventricular systolic dysfunction: 14 years after MADIT.
Implantable cardioverter-defibrillators: expanding indications and technologies.
Implantable device therapy.
Implications of multiple late gadolinium enhancement lesions on the frequency of left ventricular reverse remodeling and prognosis in patients with non-ischemic cardiomyopathy.
Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia.
Late gadolinium enhancement on cardiac magnetic resonance predicts adverse cardiovascular outcomes in nonischemic cardiomyopathy: a systematic review and meta-analysis.
Left atrial enlargement and NT-proBNP as predictors of sudden cardiac death in patients with heart failure.
Left ventricular ejection fraction overcrossing 35% after one year of cardiac resynchronization therapy predicts long term survival and freedom from sudden cardiac death: single center observational experience.
Long-term follow-up and risk assessment of arrhythmogenic right ventricular dysplasia/cardiomyopathy: personal experience from different primary and tertiary centres.
Loss of Stearoyl-CoA Desaturase 1 leads to cardiac dysfunction and lipotoxicity.
Management and outcomes of hypertrophic cardiomyopathy in young adults.
Medical therapy versus implantable cardioverter -defibrillator in preventing sudden cardiac death in patients with left ventricular systolic dysfunction and heart failure: A meta-analysis of >35,000 patients.
Modes of death and clinical outcomes in adult patients with hypertrophic cardiomyopathy in Thailand.
Myocardial Fibrosis as a Pathway of Prediction of Ventricular Arrhythmias and Sudden Cardiac Death in Patients With Nonischemic Dilated Cardiomyopathy.
Myocardial fibrosis on cardiac magnetic resonance and cardiac outcomes in hypertrophic cardiomyopathy: a meta-analysis.
Neurohormonal intervention to reduce sudden cardiac death in heart failure: what is the optimal pharmacologic strategy?
Non-sustained ventricular tachycardia as a predictor of sudden cardiac death in patients with left ventricular dysfunction: A meta-analysis.
Omega-3 Fatty acids: anti-arrhythmic, pro-arrhythmic, or both?
Overexpression of miR-221 in sudden death with cardiac hypertrophy patients.
Patient barriers to implantable cardioverter defibrillator implantation for the primary prevention of sudden cardiac death in patients with heart failure and reduced ejection fraction.
Performance of 2014 NICE defibrillator implantation guidelines in heart failure risk stratification.
Perioperative Endocarditis Management in a Patient with Homozygous Sickle Cell Disease.
Perioperative Management of Sickle Cell Disease.
Prediction of appropriate ICD therapy in patients with ischemic heart failure.
Predictive Value of Beat-to-Beat QT Variability Index Across the Continuum of Left Ventricular Dysfunction: Competing Risks of Noncardiac or Cardiovascular Death and Sudden or Nonsudden Cardiac Death.
Predictors of outcome in patients with parvovirus B19 positive endomyocardial biopsy.
Predictors of sudden cardiac death in high-risk patients following a myocardial infarction.
Primary prevention of sudden cardiac death in heart failure: will the solution be shocking?
Profiling risk from arrhythmic or hemodynamic death.
Prognostic impact of multiple fragmented QRS on cardiac events in idiopathic dilated cardiomyopathy.
Prognostic Value of LGE-CMR in HCM: A Meta-Analysis.
Prolonged Tpeak -Tend interval is a risk factor for sudden cardiac death in adults with congenital heart disease.
Protection from cardiac arrhythmia through ryanodine receptor-stabilizing protein calstabin2.
Racial differences in sudden cardiac death among hypertensive patients during antihypertensive therapy: The LIFE study.
Rationale and design of a prospective study to assess the effect of left cardiac sympathetic denervation in chronic heart failure.
Regression of electrocardiographic left ventricular hypertrophy during antihypertensive therapy and reduction in sudden cardiac death: the LIFE Study.
Relationship of Sudden Cardiac Death to New-Onset Atrial Fibrillation in Hypertensive Patients with Left Ventricular Hypertrophy.
Risk Factor and Prediction Modeling for Sudden Cardiac Death in Women With Coronary Artery Disease.
Risk factors for sudden cardiac death in patients with chronic renal insufficiency and left ventricular dysfunction.
Risk Models for Prediction of Implantable Cardioverter-Defibrillator Benefit: Insights From the DANISH Trial.
Risk stratification of ventricular arrhythmias in patients with systolic heart failure.
Role of antiarrhythmic therapy in patients at risk for sudden cardiac death: an evidence-based review.
Role of risk stratification and genetics in sudden cardiac death.
Sacubitril/Valsartan and Sudden Cardiac Death According to Implantable Cardioverter-Defibrillator Use and Heart Failure Cause: A PARADIGM-HF Analysis.
SCD in the world, Europe, Bosnia and Herzegovina and Mostar.
Secondary prevention of cardiac events following myocardial infarction: effects of atenolol and enalapril. Beijing Collaborative Study Group.
Serum markers of collagen turnover predict future shocks in implantable cardioverter-defibrillator recipients with dilated cardiomyopathy on optimal treatment.
Sinergy between drugs and devices in the fight against sudden cardiac death and heart failure.
Single-photon emission computed tomography myocardial perfusion defects are associated with an increased risk of all-cause death, cardiovascular death, and sudden cardiac death.
Sleep Apnea and Sudden Cardiac Death.
Soluble CD74 Reroutes MIF/CXCR4/AKT-Mediated Survival of Cardiac Myofibroblasts to Necroptosis.
Strategies for the prevention and treatment of sudden cardiac death.
Structural pathways and prevention of heart failure and sudden death.
Subclinical Abnormalities in Echocardiographic Parameters and Risk of Sudden Cardiac Death in a General Population: The Rotterdam Study.
Subclinical Cardiac Dysfunction Is Associated With Extracardiac Organ Damages.
Sudden Cardiac Death (SCD) - risk stratification and prediction with molecular biomarkers.
Sudden cardiac death after acute heart failure hospital admission: insights from ASCEND-HF.
Sudden cardiac death after PCI and CABG in the bare-metal stent era: Incidence, prevalence, and predictors.
Sudden cardiac death and diabetes mellitus.
Sudden cardiac death and heart failure.
Sudden cardiac death in dialysis patients: different causes and management strategies.
Sudden cardiac death in heart failure patients with preserved ejection fraction.
Sudden cardiac death in heart failure with preserved ejection fraction: a target for therapy?
Sudden cardiac death in hemodialysis patients: an in-depth review.
Sudden Cardiac Death in Patients With Atrial Fibrillation: Insights From the ENGAGE AF-TIMI 48 Trial.
Sudden cardiac death in women.
Sudden cardiac death risk prediction in heart failure with preserved ejection fraction.
Sudden cardiac death: epidemiology, causes, and mechanisms.
Sudden cardiac death: implantable cardioverter defibrillators and pharmacological treatments.
Sudden Death After Hospitalization for Heart Failure With Reduced Ejection Fraction (from the EVEREST Trial).
Sudden death in cardiac sarcoidosis: an analysis of nationwide clinical and cause-of-death registries.
Sudden death in ischemic heart disease - 2017.
Sudden death in patients with chronic bifascicular block.
Supplementary role of left ventricular global longitudinal strain for predicting sudden cardiac death in hypertrophic cardiomyopathy.
T-Wave Morphology Restitution Predicts Sudden Cardiac Death in Patients With Chronic Heart Failure.
Temporal trends in sudden cardiac death in Ontario, Canada.
The autonomic nervous system and ventricular arrhythmias in myocardial infarction and heart failure.
The clinical effectiveness and cost-effectiveness of cardiac resynchronisation (biventricular pacing) for heart failure: systematic review and economic model.
The effect of aldosterone antagonists for ventricular arrhythmia: a meta-analysis.
The effect of sacubitril/valsartan on the occurrence of ventricular arrhythmia and the risk of sudden cardiac death in patients with chronic heart failure with reduced left ventricular ejection fraction. Expert opinion of the Heart Rhythm and Heart Failure Associations of the Polish Cardiac Society.
The EP300/TP53 pathway, a suppressor of the Hippo and canonical WNT pathways, is activated in human hearts with arrhythmogenic cardiomyopathy in the absence of overt heart failure.
The J wave and fragmented QRS complexes in inferior leads associated with sudden cardiac death in patients with chronic heart failure.
The Necessity of an ICD-Therapy in Patients with Indications for Primary Prevention of Sudden Cardiac Death. One Center Experience.
The Risk of Sudden Cardiac Death in Mitral Valve Prolapse: Are All Patients Created Equal?
The role of antiarrhythmic drug therapy for the prevention of sudden cardiac death.
The role of prophylactic implantable cardioverter defibrillators in heart failure: recent trials usher in a new era of device therapy.
The SHIFT model combines clinical, electrocardiographic and echocardiographic parameters to predict sudden cardiac death in hypertrophic cardiomyopathy.
Updating the Risk Stratification for Sudden Cardiac Death in Cardiomyopathies: The Evolving Role of Cardiac Magnetic Resonance Imaging. An Approach for the Electrophysiologist.
Use of cardiac radionuclide imaging to identify patients at risk for arrhythmic sudden cardiac death.
Usefulness of Electrocardiographic Patterns at Presentation to Predict Long-term Risk of Cardiac Death in Patients With Hypertrophic Cardiomyopathy.
Usefulness of Single Nucleotide Polymorphisms as Predictors of Sudden Cardiac Death.
Ventricular tachycardia and sudden cardiac death.
Vitamin D deficiency is associated with sudden cardiac death, combined cardiovascular events, and mortality in haemodialysis patients.
[Blood transfusion assessment to 112 homozygous sickle-cell disease patients in university hospital of Brazzaville.]
[Congestive heart failure and sudden cardiac death: Pharmacological and non pharmacological treatment strategies].
[Heart failure and mortality: polyunsaturated fatty acids and the relevance of evidence].
[Heart failure and sudden cardiac death: pharmacological and nonpharmacological treatment possibilities from the viewpoint of the rhythmologist]
[Implantable cardioverter-defibrillator in patients with chronic heart failure]
[In Process Citation]
[Prevention of sudden cardiac death]
[Primary prevention of sudden cardiac death implanted cardioverter defibrillator (ICD) versus antiarrhythmic drugs]
[Wearable cardioverter-defibrillators: clinical experience and future perspectives].
Heart Failure, Diastolic
Cardiovascular magnetic resonance imaging in hypertrophic cardiomyopathy: Current state of the art.
Incidence and predictors of sudden cardiac death in patients with diastolic heart failure.
Sickle cell disease: at the crossroads of pulmonary hypertension and diastolic heart failure.
Heart Failure, Systolic
Current Device Therapies for Sudden Cardiac Death Prevention - the ICD, Subcutaneous ICD and Wearable ICD.
Duration of Heart Failure and Effect of Defibrillator Implantation in Patients With Nonischemic Systolic Heart Failure.
Update on primary prevention implantable cardioverter-defibrillator therapy.
Heart Neoplasms
Benign cardiac tumours associated with sudden death.
Heart Valve Diseases
Ischemic Heart Disease Related Sudden Cardiac Death in Autopsied Cases: An Egyptian perspective.
Sudden cardiac death from structural heart diseases in adults: imaging findings with cardiovascular computed tomography and magnetic resonance.
Sudden Cardiac Death Risk Prediction: The Role of Cardiac Magnetic Resonance Imaging.
The spectrum of epidemiology underlying sudden cardiac death.
[Antiarrhythmic agents in the prevention of sudden cardiac death]
Hematologic Diseases
Dynamics of deformable straight and curved prolate capsules in simple shear flow.
Hematologic Neoplasms
Allogeneic hematopoietic stem cell transplant for sickle cell disease: The why, who, and what.
Characterization of Hematopoiesis in Sickle Cell Disease by Prospective Isolation of Stem and Progenitor Cells.
Hodgkin lymphoma in a child with sickle cell anemia.
Pomalidomide augments fetal hemoglobin production without the myelosuppressive effects of hydroxyurea in transgenic sickle cell mice.
Treatment and outcomes of hepatocellular carcinoma in patients with Sickle cell disease: a population-based study in the U.S.
Hematoma, Epidural, Cranial
Cranial epidural hematomas: A case series and literature review of this rare complication associated with sickle cell disease.
Hematuria
A novel case report of sickle cell disease-associated immunoglobulin A nephropathy: the diagnostic value of erythrocyte dysmorphism evaluation.
Bleeding in patients with sickle cell disease: a population-based study.
Renal abnormalities in sickle cell disease.
Hemochromatosis
Fertility challenges for women with sickle cell disease.
Hemoglobin C Disease
Assessment of Hemoglobin Variants in Patients Receiving Health Care at the Ho Teaching Hospital: A Three-Year Retrospective Study.
Brain Perfusion Impairment in Neurologically Asymptomatic Adult Patients with Sickle-Cell Disease Shown by Voxel-Based Analysis of SPECT Images.
Point-of-care screening for sickle cell disease in low-resource settings: A multi-center evaluation of HemoTypeSC, a novel rapid test.
Prophylactic penicillin after 5 years of age in patients with sickle cell disease: A survey of sickle cell disease experts.
Severe proliferative retinopathy is associated with blood hyperviscosity in sickle cell hemoglobin-C disease but not in sickle cell anemia.
Hemoglobin SC Disease
Adverse neurological outcomes in Nigerian children with sickle cell disease.
Associations between TGF-?1 Levels and Markers of Hemolysis, Inflammation, and Tissue Remodeling in Pediatric Sickle Cell Patients.
Clinical phenotypes and outcomes of precapillary pulmonary hypertension of sickle cell disease.
Combination erythropoietin-hydroxyurea therapy in sickle cell disease: experience from the National Institutes of Health and a literature review.
Herbal Drug Use In Sickle Cell Disease Management; Trends And Perspectives In Sub-Saharan Africa.
Impaired pubertal development and testicular hormone function in males with sickle cell anemia.
Management of Sickle Cell Disease in Children.
Methodological aspects of oxygen gradient ektacytometry in sickle cell disease: Effects of sample storage on outcome parameters in distinct patient subgroups.
Progressive Decline in Estimated GFR in Patients With Sickle Cell Disease: An Observational Cohort Study.
The increasing prevalence of childhood sickle-cell disease in Ireland.
Whole blood viscosity and red blood cell adhesion: Potential biomarkers for targeted and curative therapies in sickle cell disease.
Hemoglobinopathies
Analysis of clinical presentation, hematological factors, self-reported bed net usage, and malaria burden in sickle cell disease patients.
BEHAVIORAL CHARACTERISTICS OF CHILDREN WITH SICKLE CELL DISEASE.
Combined use of nonmyelosuppressive nitrosourea analogues with hydroxyurea in the induction of F-cell production in a human erythroleukemic cell line.
Comparative evaluation of oral and dento-maxillofacial manifestation of patients with sickle cell diseases and beta thalassemia major.
Current challenges in the management of patients with sickle cell disease - A report of the Italian experience.
Development of interactive algorithm for clinical management of acute events related to sickle cell disease in emergency department.
Effectiveness of preoperative screening for sickle cell disease in a population with a newborn screening program: a cohort study.
Emergency management of sickle cell disease complications: review and practice guidelines.
Emergency Medicine Management of Sickle Cell Disease Complications: An Evidence-Based Update.
Evaluation of Technical Issues in a Pilot Multicenter Newborn Screening Program for Sickle Cell Disease.
Gene therapy in thalassemia and hemoglobinopathies.
Genetic determinants and stroke in children with sickle cell disease.
Health-related quality of life of adolescents with sickle cell disease in sub-Saharan Africa: a cross-sectional study.
Hemoglobin disorders and endothelial cell interactions.
Hemoglobinopathies and Stroke: Strategies for Prevention and Treatment.
Hemostatic abnormalities in sickle cell disease.
HemoTypeSC point-of-care testing shows high sensitivity with alkaline cellulose acetate hemoglobin electrophoresis for screening hemoglobin SS and SC genotypes.
History and current status of newborn screening for hemoglobinopathies.
HRI depletion cooperates with pharmacologic inducers to elevate fetal hemoglobin and reduce sickle cell formation.
Infections and immunizations of children with sickle cell disease.
Inflammation in Sickle Cell Disease: Differential and Down-Expressed Plasma Levels of Annexin A1 Protein.
Intestine-specific Disruption of Hypoxia-inducible Factor (HIF)-2? Improves Anemia in Sickle Cell Disease.
Iron metabolism and iron chelation in sickle cell disease.
Levels of tumor necrosis factor alpha/cachectin (TNF alpha) in sera from patients with sickle cell disease.
Low cobalamin levels in African Americans with and without sickle cell disease.
Manual erythroexchange in sickle cell disease: multicenter validation of a protocol predictive of volume to exchange and hemoglobin values.
Maternal sickle cell anemia and neonatal isoimmunization.
Mixed Bullous-Eczematous Contact Dermatitis From a Black Henna Tattoo in an African American Female With Sickle Cell Disease With Post-Dermatitis Pain.
Newborn Screening for Sickle Cell Disease and Other Hemoglobinopathies: A Short Review on Classical Laboratory Methods-Isoelectric Focusing, HPLC, and Capillary Electrophoresis.
Newborn Screening for Sickle Cell Disease in Liberia: A Pilot Study.
Newborn screening for sickle cell disease: an innovative pilot program to improve child survival in Dar es Salaam, Tanzania.
Newborn screening for sickle cell disease: technical and legal aspects of a German pilot study with 38,220 participants.
Pediatric Hematology Providers on Referral for Transplant Evaluation for Sickle Cell Disease: A Regional Perspective.
Placenta growth factor augments airway hyperresponsiveness via leukotrienes and IL-13.
Plasma levels of TGF-?1 in homeostasis of the inflammation in sickle cell disease.
Population estimates of sickle cell disease in the U.S.
Posterior Reversible Encephalopathy Syndrome after Hematopoietic Cell Transplantation in Children with Hemoglobinopathies.
Potent and orally active purine-based fetal hemoglobin inducers for treating ?-thalassemia and sickle cell disease.
Pregnancy in sickle cell disease: maternal and fetal outcomes in a population receiving prophylactic partial exchange transfusions.
Pregnancy outcomes among patients with sickle cell disease at Korle-Bu Teaching Hospital, Accra, Ghana: retrospective cohort study.
Providing Genetic Risk Information to Parents of Newborns with Sickle Cell Trait: Role of the General Practitioner in Neonatal Screening.
Reproductive intentions in mothers of young children with sickle cell disease.
Serum Hepcidin Concentration in Individuals with Sickle Cell Anemia: Basis for the Dietary Recommendation of Iron.
Sickle cell anemia/sickle cell disease and pregnancy outcomes among ethnic tribes in India: an integrative mini-review.
Sickle cell disease patients with and without extremely high hospital use: pain, opioids, and coping.
Sickle cell disease: health promotion and maintenance and the role of primary care nurse practitioners.
Sickle-cell anemia and pulmonary hypertension.
The clinical impact of MTHFR polymorphism on the vascular complications of sickle cell disease.
The kidney in sickle hemoglobinopathies?.
The prevalence of priapism in children and adolescents with sickle cell disease in Brazil.
Updated Worldwide Epidemiology of Inherited Erythrocyte Disorders.
Whole blood viscosity and red blood cell adhesion: Potential biomarkers for targeted and curative therapies in sickle cell disease.
Zinc status of children with sickle cell disease: relationship to poor growth.
[S hemoglobinopathies in Argentina]
Hemoglobinuria
All-Cause Mortality and Incidence of Major Adverse Cardiac Events in Sickle Cell Nephropathy: A Comparative Study.
Defective regulation of complement by the sickle erythrocyte: evidence for a defect in control of membrane attack complex formation.
Delayed hemolytic transfusion reaction/hyperhemolysis syndrome in children with sickle cell disease.
Pulmonary hypertension and nitric oxide depletion in sickle cell disease.
Hemoglobinuria, Paroxysmal
Defective regulation of complement by the sickle erythrocyte: evidence for a defect in control of membrane attack complex formation.
Pulmonary hypertension and nitric oxide depletion in sickle cell disease.
Hemolytic-Uremic Syndrome
Hemopexin and haptoglobin: allies against heme toxicity from hemoglobin not contenders.
Laparoscopic splenic procedures in children: experience in 231 children.
Hemophilia A
The increasing prevalence of childhood sickle-cell disease in Ireland.
Hemorrhagic Stroke
Association of HIV infection with clinical and laboratory characteristics of sickle cell disease.
Neurologic complications in children under five years with sickle cell disease.
Nonaneurysmal Subarachnoid Hemorrhage in Sickle Cell Disease: Description of a Case and a Review of the Literature.
The excess burden of stroke in hospitalized adults with sickle cell disease.
[Silent microhemorrhages in patients with symptomatic cerebrovascular disease.]
Hemosiderosis
Gastrointestinal and Hepatic Complications of Sickle Cell Disease.
Magnetic resonance detection of kidney iron deposition in sickle cell disease: a marker of chronic hemolysis.
The Histopathologic Features of Sickle Cell HepatopathyA Multi-Institutional Study.
Hepatitis
Gastrointestinal and Hepatic Complications of Sickle Cell Disease.
Liver function tests in sickle cell disease.
Liver transplantation in children with sickle-cell disease.
Successful treatment of chronic hepatitis C virus infection with peginterferon alpha-2a and ribavirin in patients with sickle cell disease.
Hepatitis B
Diminished antibody response to hepatitis B immunization in children with sickle cell disease.
Hepatitis B and C viral markers in patients with sickle cell disease in Ibadan, Nigeria.
Investigation of diagnostic utility and expression profiles of stem cell markers (CD133 and CD90) in hepatocellular carcinoma, small cell dysplasia, and cirrhosis.
Liver function tests in sickle cell disease.
Prevalence of Hepatitis B, Hepatitis C, and HIV in Multiply Transfused Sickle Cell Disease Patients from Oman.
Sickle cell disease is associated with decreased HIV but higher HBV and HCV comorbidities in US hospital discharge records: a cross-sectional study.
[Human immunodeficiency virus, hepatitis C virus and hepatitis B viruses in patients with sickle-cell disease in Togo]
Hepatitis B, Chronic
[Expression of c-erbB-2 protein and EGF receptor in hepatitis B, cirrhosis and hepatocellular carcinoma]
Hepatitis C
HLA-G polymorphism influences the susceptibility to HCV infection in sickle cell disease patients.
Liver function tests in sickle cell disease.
Long-term outcomes of donation after cardiac death liver allografts from a single center.
Prevalence of serologic markers of transfusion and sexually transmitted infections and their correlation with clinical features in a large cohort of Brazilian patients with sickle cell disease.
Sickle cell disease is associated with decreased HIV but higher HBV and HCV comorbidities in US hospital discharge records: a cross-sectional study.
Stearoyl coenzyme A desaturase 1 is associated with hepatitis C virus replication complex and regulates viral replication.
Stearoyl-CoA desaturase inhibition blocks formation of hepatitis C virus-induced specialized membranes.
Stearoyl-CoA desaturase-1 is required for flavivirus RNA replication.
Superimposed Hepatitis C Virus in Sickle Cell Disease Pregnant Woman.
[Human immunodeficiency virus, hepatitis C virus and hepatitis B viruses in patients with sickle-cell disease in Togo]
Hepatitis, Autoimmune
Autoimmune Liver Disease in Patients With Sickle Cell Disease.
Hepatoblastoma
Regulation of stearoyl-CoA desaturase activity by the trans-10,cis-12 isomer of conjugated linoleic acid in HepG2 cells.
Hepatomegaly
Frequency of hepatomegaly and splenomegaly in Nigerian patients with sickle cell disease.
Impaired bile secretion promotes hepatobiliary injury in Sickle Cell Disease.
Malaria in patients with sickle cell anaemia: burden, risk factors and outcome at the Laquintinie hospital, Cameroon.
Multiple complications in sickle cell anaemia.
Sonographic Assessment of Some Abdominal Organs in Children with Sickle Cell Disease in Ilorin, Nigeria.
Sonographic Evaluation of Some Abdominal Organs in Sickle Cell Disease Patients in a Tertiary Health Institution in Northeastern Nigeria.
Herpes Zoster
Severe infection including disseminated herpes zoster triggered by subclinical Cushing's disease: a case report.
HIV Infections
Association of HIV Infection and Antiretroviral Therapy With Sudden Cardiac Death.
Association of HIV infection with clinical and laboratory characteristics of sickle cell disease.
Children with sickle cell disease and human immunodeficiency virus-1 infection: use of inpatient care services in the United States.
HIV Infection and the Risk of World Health Organization-Defined Sudden Cardiac Death.
Influence of sickle cell disease on susceptibility to HIV infection.
Prevalence and Factors Associated with Human Parvovirus B19 Infection in Sickle Cell Patients Hospitalized in Tanzania.
Severe pneumococcal sepsis and meningitis in human immunodeficiency virus-infected adults with sickle cell disease.
Severe pre-eclampsia among pregnant women with sickle cell disease and HIV.
Sickle cell disease is associated with decreased HIV but higher HBV and HCV comorbidities in US hospital discharge records: a cross-sectional study.
The interaction between sickle cell disease and HIV infection: a systematic review.
Unexplained lymphadenopathy in sickle cell disease.
Hodgkin Disease
Management of Hodgkin Lymphoma in a Sickle Cell Patient: A Case Report.
Homocystinuria
Cystathionine ?-synthase-deficient mice thrive on a low-methionine diet.
Leptin concentrations and SCD-1 indices in classical homocystinuria: Evidence for the role of sulfur amino acids in the regulation of lipid metabolism.
HTLV-I Infections
Chronic progressive spinocerebellar syndrome associated with antibodies to human T-lymphotropic virus type I: clinico-virological and magnetic resonance imaging studies.
Huntington Disease
[A case of adult-onset Huntington disease presenting with spasticity and cerebellar ataxia, mimicking spinocerebellar degeneration]
Hyperacusis
Bone-conduction hyperacusis induced by superior canal dehiscence in human: the underlying mechanism.
Underwater Endoscopic Repair of Superior Canal Dehiscence.
Hyperalgesia
Bartonella henselae Infection in Sickle Cell Disease Mice Is Associated with Hyperalgesia.
Dexmedetomidine ameliorates nocifensive behavior in humanized sickle cell mice.
Effect of Inhaled Cannabis for Pain in Adults With Sickle Cell Disease: A Randomized Clinical Trial.
Heme Causes Pain in Sickle Mice via Toll-Like Receptor 4-Mediated Reactive Oxygen Species- and Endoplasmic Reticulum Stress-Induced Glial Activation.
Sensitivities to Thermal and Mechanical Stimuli: Adults with Sickle Cell Disease Compared to Healthy, Pain-free African American Controls.
Sensitization of C-fiber nociceptors in mice with sickle cell disease is decreased by local inhibition of anandamide hydrolysis.
Sensitization of nociceptive spinal neurons contributes to pain in a transgenic model of sickle cell disease.
Sensitization of nociceptors by prostaglandin E2-glycerol contributes to hyperalgesia in mice with sickle cell disease.
Sensory and Thermal Quantitative Testing in Children With Sickle Cell Disease.
Sickle cell mice exhibit mechanical allodynia and enhanced responsiveness in light touch cutaneous mechanoreceptors.
Substance P modulates electroacupuncture analgesia in humanized mice with sickle cell disease.
Hypercalcemia
Primary Hyperparathyroidism in Sickle Cell Disease: An Unknown Complication of the Disease in Adulthood.
Hypercholesterolemia
A dominant negative form of the transcription factor c-Jun affects genes that have opposing effects on lipid homeostasis in mice.
Altered metabolic responses to intermittent hypoxia in mice with partial deficiency of hypoxia-inducible factor-1alpha.
Differential diagnosis of Schnyder corneal dystrophy.
Effects of Bacillus polyfermenticus SCD on lipid and antioxidant metabolisms in rats fed a high-fat and high-cholesterol diet.
Inhibition of stearoyl CoA desaturase activity induces hypercholesterolemia in the cholesterol-fed hamster.
L-4F, an apolipoprotein A-1 mimetic, dramatically improves vasodilation in hypercholesterolemia and sickle cell disease.
Liver gene expression analysis reveals endoplasmic reticulum stress and metabolic dysfunction in SCD1-deficient mice fed a very low-fat diet.
Stearoyl-CoA desaturase deficiency, hypercholesterolemia, cholestasis, and diabetes.
Sudden Cardiac Death in Young Adult.
Sudden Cardiac Death Risk in Downhill Skiers and Mountain Hikers and Specific Prevention Strategies.
Hyperemia
Cerebral hyperemia, stroke, and transfusion in sickle cell disease.
Dynamic vascular analysis shows a hyperemic flow pattern in sickle cell disease.
Sickle cell microvascular paradox-oxygen supply-demand mismatch.
Skin Capillary Density and Microvascular Reactivity in Obese Subjects with and without Metabolic Syndrome.
Hyperglycemia
Dysrhythmia and electrocardiographic changes in diabetes mellitus: pathophysiology and impact on the incidence of sudden cardiac death.
Hemoglobin A1c Levels and Risk of Sudden Cardiac Death - a Nested Case-Control Study.
Kynurenine-Induced Aryl Hydrocarbon Receptor Signaling in Mice Causes Body Mass Gain, Liver Steatosis, and Hyperglycemia.
Pre-germinated brown rice extract ameliorates high-fat diet-induced metabolic syndrome.
Remote ischemic preconditioning differentially attenuates post-ischemic cardiac arrhythmia in streptozotocin-induced diabetic versus nondiabetic rats.
Site and mechanism of leptin action in a rodent form of congenital lipodystrophy.
Hyperhidrosis
Aborted sudden cardiac death and a mother with suspected metabolic myopathy.
Hyperhomocysteinemia
Correlation of the C677T MTHFR genotype with homocysteine levels in children with sickle cell disease.
Homocysteine in sickle cell disease: relationship to stroke.
Hyperhomocysteinemia is associated with low plasma pyridoxine levels in children with sickle cell disease.
Mild hyperhomocysteinemia in adult patients with sickle cell disease: a common finding unrelated to folate and cobalamin status.
Hyperinsulinism
Site and mechanism of leptin action in a rodent form of congenital lipodystrophy.
Soy protein reduces hepatic lipotoxicity in hyperinsulinemic obese Zucker fa/fa rats.
Hyperkalemia
Combined effect of renal function and serum potassium level in sudden cardiac death in aging hypertensive subjects.
Current Perspectives on Sudden Cardiac Death in Hemodialysis Patients.
Intravenous infusion of haptoglobin for the prevention of adverse clinical outcome in Sickle Cell Disease.
Low Potassium Dialysate as a Protective Factor of Sudden Cardiac Death in Hemodialysis Patients with Hyperkalemia.
Serum Potassium Levels and Risk of Sudden Cardiac Death Among Patients With Chronic Kidney Disease and Significant Coronary Artery Disease.
Hyperlipidemia, Familial Combined
Association of stearoyl-CoA desaturase 1 activity with familial combined hyperlipidemia.
Hyperlipidemias
Aqueous extract of post-fermented tea reverts the hepatic steatosis of hyperlipidemia rat by regulating the lipogenic genes expression and hepatic fatty acid composition.
Association of stearoyl-CoA desaturase 1 activity with familial combined hyperlipidemia.
Beneficial Effects of SREBP Decoy Oligodeoxynucleotide in an Animal Model of Hyperlipidemia.
Citrus flavonoids repress the mRNA for stearoyl-CoA desaturase, a key enzyme in lipid synthesis and obesity control, in rat primary hepatocytes.
Discovery of novel liver X receptor inverse agonists as lipogenesis inhibitors.
Hyperlipidemia and lipid peroxidation are dependent on the severity of chronic intermittent hypoxia.
Obstructive sleep apnea and dyslipidemia: implications for atherosclerosis.
Pediococcus pentosaceus PP04 Ameliorates High-Fat Diet-Induced Hyperlipidemia by Regulating Lipid Metabolism in C57BL/6N Mice.
Relationship between stearoyl-CoA desaturase activity and plasma triglycerides in human and mouse hypertriglyceridemia.
Role of stearoyl-coenzyme A desaturase in regulating lipid metabolism.
Stearoyl-CoA desaturase, a short-lived protein of endoplasmic reticulum with multiple control mechanisms.
Hyperparathyroidism, Secondary
Response to Long-term Vitamin D Therapy for Bone Disease in Children With Sickle Cell Disease.
Hyperpigmentation
Erythema ab igne in patients with sickle cell disease.
Severity in phenotypic expression of homozygous sickle cell disease (Hb.SS) - Does hypermelanotic or hypomelanotic skin status of affected patients play a role?
Hypersensitivity
Airway inflammation in sickle cell disease-A translational perspective.
Asthma in children with sickle cell disease and its association with acute chest syndrome.
Asthma, allergic sensitization and lung function in sickle cell disease.
Bartonella henselae Infection in Sickle Cell Disease Mice Is Associated with Hyperalgesia.
Chemokine (c-c motif) receptor 2 mediates mechanical and cold hypersensitivity in sickle cell disease mice.
Children and adolescents with sickle cell disease have worse cold and mechanical hypersensitivity during acute painful events.
Contact dermatitis as a systemic disease.
Effectiveness of different click stimuli in diagnosing superior canal dehiscence using cervical vestibular evoked myogenic potentials.
Gabapentin alleviates chronic spontaneous pain and acute hypoxia-related pain in a mouse model of sickle cell disease.
Metal allergy and systemic contact dermatitis: an overview.
Patients with sickle cell disease have increased sensitivity to cold and heat.
Progressive vasoconstriction with sequential thermal stimulation indicates vascular dysautonomia in sickle cell disease.
Sickle Cell Disease and HIV: A Case Highlighting Management Challenges for Children in a Resource-Limited Setting.
Systemic contact dermatitis and allergy to biomedical devices.
Systemic contact dermatitis.
Systemic Contact Dermatitis: A review.
Toll-like receptor signaling links dietary fatty acids to the metabolic syndrome.
Transient receptor potential vanilloid 1 mediates pain in mice with severe sickle cell disease.
Hypersensitivity, Delayed
Zinc deficiency and blood lymphocyte function with sickle cell disease.
Hypersplenism
Splenectomy for haematological disorders: A single center study in 150 patients from Oman.
Splenectomy for hematological diseases: The Qatif Central Hospital experience.
Hypertension
A new hypotensive polyunsaturated fatty acid dietary combination regulates oleic acid accumulation by suppression of stearoyl CoA desaturase 1 gene expression in the SHR model of genetic hypertension.
Abnormal Ambulatory Blood Pressure and Early Renal Dysfunction in Sickle Cell Disease.
Acute, Bilateral, Concurrent Central Retinal Artery Occlusion in Sickle Cell Disease After Use of Tadalafil (Cialis).
Age-dependent association between hepatic lipase gene C-480T polymorphism and the risk of pre-hospital sudden cardiac death: the Helsinki Sudden Death Study.
Ambulatory hypertension in a pediatric cohort of sickle cell disease.
Ambulatory Hypertension in Pediatric Patients With Sickle Cell Disease and Its Association With End-Organ Damage.
An epidemiologic and histopathological study of sudden cardiac death in Osaka Medical Examiner's Office.
Analysis of Risk Factors Associated With Poor Outcome in Posterior Reversible Encephalopathy Syndrome After Treatment in Children: Systematic Review and Meta-Analysis.
Association of low-density lipoprotein receptor-related protein 1 rs11613352 and angiopoietin-like 3 rs2131925 with hypertension in men-the Tampere adult population cardiovascular risk study.
Atypical presentation of acute post-infectious glomerulonephritis in patients with sickle cell disease: report of two cases.
Birthplace predicts risk for prehospital sudden cardiac death in middle-aged men who migrated to metropolitan area: The Helsinki Sudden Death Study.
Blood pressure in acute vaso-occlusive crises of sickle cell disease.
Blood pressure, hypertension and the risk of sudden cardiac death: a systematic review and meta-analysis of cohort studies.
Bringing Critical Race Praxis Into the Study of Electrophysiological Substrate of Sudden Cardiac Death: The ARIC Study.
Cardiorespiratory Fitness and Risk of Sudden Cardiac Death in Men and Women in the United States: A Prospective Evaluation From the Aerobics Center Longitudinal Study.
Certain beta blockers (e.g., bisoprolol) may be reevaluated in hypertension guidelines for patients with left ventricular hypertrophy to diminish the ventricular arrhythmic risk.
Clinical prediction of genotypes in hypertrophic cardiomyopathy: A systematic review.
Competing risk analysis of cause-specific mortality in patients with an implantable cardioverter-defibrillator: The EVADEF cohort study.
Dialysis modality-related disparities in sudden cardiac death: hemodialysis versus peritoneal dialysis.
Do insomnia complaints cause hypertension or cardiovascular disease?
Ectasia of the basilar artery in children with sickle cell disease: Relationship to hematocrit and psychometric measures.
Effect of sucrose addition to drinking water, that induces hypertension in the rats, on liver microsomal Delta9 and Delta5-desaturase activities.
Electrocardiographic and clinical predictors separating atherosclerotic sudden cardiac death from incident coronary heart disease.
Genetic contributions to the expression of acquired causes of cardiac hypertrophy in non-ischemic sudden cardiac death victims.
Global Electric Heterogeneity Risk Score for Prediction of Sudden Cardiac Death in the General Population: The Atherosclerosis Risk in Communities (ARIC) and Cardiovascular Health (CHS) Studies.
Hospitalization for pain in patients with sickle cell disease treated with sildenafil for elevated TRV and low exercise capacity.
Hypertension in standard criteria deceased donors is associated with inferior outcomes following kidney transplantation.
Hypertension Is a Risk Factor for Several Types of Heart Disease: Review of Prospective Studies.
Impact of Korea Network for Organ Sharing Expanded Donor Criteria on Delayed Graft Fuction in Kidney Transplantation: A Single-Center Experience.
Interleukin 18 gene promoter polymorphism: a link between hypertension and pre-hospital sudden cardiac death: the Helsinki Sudden Death Study.
Large-vessel occlusion in sickle cell disease: pathogenesis, clinical consequences, and therapeutic implications.
Long-term outcomes of kidney transplantation from expanded criteria deceased donors at a single center: comparison with standard criteria deceased donors.
Nocturnal hypertension associated with stroke and silent cerebral infarcts in children with sickle cell disease.
NT-pro brain natriuretic peptide levels and the risk of death in the cooperative study of sickle cell disease.
Outcomes of Kidney Transplant Recipients with Sickle Cell Disease: An Analysis of the 2000-2019 UNOS/OPTN Database.
Platelet activation in patients with sickle disease, hemolysis-associated pulmonary hypertension, and nitric oxide scavenging by cell-free hemoglobin.
Polymorphisms within the angiotensinogen gene (GT-repeat) and the risk of stroke in pediatric patients with sickle cell disease: a case-control study.
Posterior Reversible Encephalopathy Syndrome after Hematopoietic Cell Transplantation in Children with Hemoglobinopathies.
Predictors of sudden cardiac death in atrial fibrillation: The Atherosclerosis Risk in Communities (ARIC) study.
Prevalence and risk factors for pulmonary artery systolic hypertension among sickle cell disease patients in Nigeria.
Prevention of ventricular fibrillation, acute myocardial infarction (myocardial necrosis), heart failure, and mortality by bretylium: is ischemic heart disease primarily adrenergic cardiovascular disease?
Prior myocardial infarction is the major risk factor associated with sudden cardiac death during downhill skiing.
Prospective study of sudden cardiac death among women in the United States.
Pulmonary hypertension of sickle cell disease: more than just another lung disease.
Racial and ethnic disparities in subjective cognitive decline: a closer look, United States, 2015-2018.
Recent advances on stearoyl-CoA desaturase regulation in fatty liver diseases.
Relationship Between Anemia and Sudden Cardiac Death in Patients with Severe Aortic Stenosis.
Results of Kidney Transplantation from Expanded Criteria Donors: A Single-Center Experience.
Review: Hemodynamic Characteristics and Outcomes of Sickle Cell Disease Associated Pulmonary Hypertension.
RR-QT interval trend covariability for sudden cardiac death risk stratification.
Severe COVID-19 with acute respiratory distress syndrome (ARDS) in a sickle cell disease adult patient: case report.
Similar burden of type 2 diabetes among adult patients with sickle cell disease relative to African Americans in the U.S. population: a six-year population-based cohort analysis.
Single-photon emission computed tomography myocardial perfusion imaging and the risk of sudden cardiac death in patients with coronary disease and left ventricular ejection fraction>35%.
Skeletal Muscle Characteristics of Rats with Obesity, Diabetes, Hypertension, and Hyperlipidemia.
Sudden Cardiac Death Among Firefighters ?45 Years of Age in the United States.
Sudden cardiac death in cardiac transplant recipients.
Sudden Cardiac Death in Hypertensive Patients.
Sudden Cardiac Death in India: A Growing Concern.
Sudden cardiac death in neuromuscular disorders.
Sudden cardiac death in the Kazakh and Han peoples of Xinjiang, China: A comparative cross-sectional study.
Sudden Cardiac Death Risk in Downhill Skiers and Mountain Hikers and Specific Prevention Strategies.
Sudden death in schizophrenia.
The Benefits of High-Intensity Interval Training on Cognition and Blood Pressure in Older Adults With Hypertension and Subjective Cognitive Decline: Results From the Heart & Mind Study.
The emerging challenge of optimal blood pressure management and hypertensive syndromes in pregnant women with sickle cell disease: a review.
The glomerulopathy of sickle cell disease.
The interaction between sickle cell disease and HIV infection: a systematic review.
The prevalence of hypertension and abnormal kidney function in children with sickle cell disease -a cross sectional review.
The relationship of sleep duration and insomnia to risk of hypertension incidence: a meta-analysis of prospective cohort studies.
The worsening of left ventricular hypertrophy is the strongest predictor of sudden cardiac death in haemodialysis patients: a 10 year survey.
Treatment of Elderly Hypertensive Patients with Epithelial Sodium Channel Inhibitors Combined with a Thiazide Diuretic Reduces Coronary Mortality and Sudden Cardiac Death.
Unmasking hypertension in children and adolescents with sickle/beta-thalassemia.
[Arterial hypertension and sudden cardiac death]
[Pathophysiological consequences of hemolysis. Role of cell-free hemoglobin].
[Prevention of coronary disease and sudden death by nutrition]
[Sudden cardiac death in diabetes mellitus].
[Sudden Cardiac Death in Patients With Chronic Obstructive Pulmonary Disease].
Hypertension, Portal
Portal hypertension evolving from sickled hepatopathy: Could hepatic venous Doppler ultrasound be beneficial in its evaluation?
Hypertension, Pulmonary
A novel molecular signature for elevated tricuspid regurgitation velocity in sickle cell disease.
Abnormalities in Cardiac Structure and Function in Adults with Sickle Cell Disease are not Associated with Pulmonary Hypertension.
Acute kidney injury in sickle patients with painful crisis or acute chest syndrome and its relation to pulmonary hypertension.
All-Cause Mortality and Incidence of Major Adverse Cardiac Events in Sickle Cell Nephropathy: A Comparative Study.
Arterial Stiffness Impairment in Sickle Cell Disease Associated with Chronic Vascular Complications: The Multinational African CADRE Study.
Assessment of cystatin C in pediatric sickle cell disease and ?-thalassemia as a marker of subclinical cardiovascular dysfunction: a case-control study.
Association of HIV infection with clinical and laboratory characteristics of sickle cell disease.
Association of pro-inflammatory high-density lipoprotein cholesterol with clinical and laboratory variables in sickle cell disease.
Asthma management: reinventing the wheel in sickle cell disease.
Calpain-1 regulates platelet function in a humanized mouse model of sickle cell disease.
Cardiomyopathy With Restrictive Physiology in Sickle Cell Disease.
Changes in Bi-ventricular Function After Hematopoietic Stem Cell Transplant as Assessed by Speckle Tracking Echocardiography.
Chronic blood exchange transfusions in the management of pre-capillary pulmonary hypertension complicating sickle cell disease.
Chronic Pulmonary Complications of Sickle Cell Disease.
Chronic sickle cell lung disease: new insights into the diagnosis, pathogenesis and treatment of pulmonary hypertension.
Circulating platelet and erythrocyte microparticles in young children and adolescents with sickle cell disease: Relation to cardiovascular complications.
Clinical correlates of acute pulmonary events in children and adolescents with sickle cell disease.
Clinical management of adult sickle-cell disease.
Determinants of Sudden Cardiac Death in Adult Patients With Eisenmenger Syndrome.
Diastolic dysfunction and pulmonary hypertension in sickle cell anemia: is there a role for L-carnitine treatment?
Diastolic dysfunction is an independent risk factor for death in patients with sickle cell disease.
Echocardiographic abnormalities in sickle cell disease.
Effects of Red Blood Cell Sickling on Right Ventricular Afterload in vivo.
Elevated Circulating Stromal-Derived Factor-1 Levels in Sickle Cell Disease.
Endothelin receptor antagonists for pulmonary hypertension in adult patients with sickle cell disease.
Erythropoietin-mediated expression of placenta growth factor is regulated via activation of hypoxia-inducible factor-1? and post-transcriptionally by miR-214 in sickle cell disease.
Exercise tolerance, lung function abnormalities, anemia, and cardiothoracic ratio in sickle cell patients.
Genetic modifiers of severity in sickle cell disease.
Genetics of Sickle Cell-Associated Cardiovascular Disease: An Expert Review with Lessons Learned in Africa.
Genomic polymorphisms in sickle cell disease: implications for clinical diversity and treatment.
Heme-bound iron activates placenta growth factor in erythroid cells via erythroid Krüppel-like factor.
Hemoglobin disorders and endothelial cell interactions.
Hemopexin dosing improves cardiopulmonary dysfunction in murine sickle cell disease.
In vitro evidence of the inhibitory capacity of chloroquine on arginase activity in sickle erythrocytes.
In-hospital Outcomes and Characteristics of Heart Failure in Sickle Cell Disease.
Increased Red Blood Cell Stiffness Increases Pulmonary Vascular Resistance and Pulmonary Arterial Pressure.
Inflammation in sickle cell disease.
Left Ventricular Structural and Functional Changes in Children With ?-Thalassemia and Sickle Cell Disease: Relationship to Sleep-disordered Breathing.
Long Term Outcome and Evaluation of Organ Function in Pediatric Patients Undergoing Haploidentical and Matched Related Hematopoietic Cell Transplantation for Sickle Cell Disease.
Mechanisms of vasculopathy in sickle cell disease and thalassemia.
Microfluidics in Sickle Cell Disease Research: State of the Art and a Perspective Beyond the Flow Problem.
Mutations and polymorphisms in hemoglobin genes and the risk of pulmonary hypertension and death in sickle cell disease.
N-terminal pro-brain natriuretic peptide levels and risk of death in sickle cell disease.
NT-proBNP levels and cardiopulmonary function in children with sickle cell disease.
Paediatric sickle cell disease: pulmonary hypertension but normal vascular resistance.
Pathophysiology and treatment of pulmonary hypertension in sickle cell disease.
Platelet activation in patients with sickle disease, hemolysis-associated pulmonary hypertension, and nitric oxide scavenging by cell-free hemoglobin.
Predictors of Diffusing Capacity in Children With Sickle Cell Disease: A Longitudinal Study.
Prevalence and risk factors for pulmonary artery systolic hypertension among sickle cell disease patients in Nigeria.
Prevalence of pulmonary hypertension in sickle cell anaemia patients of a tertiary hospital in Nigeria.
Prolonged QTc interval in children and young adults with sickle cell disease at steady state.
Proteinuria is associated with elevated tricuspid regurgitant jet velocity in children with sickle cell disease.
Pulmonary complications of hemoglobinopathies.
Pulmonary complications of sickle cell disease.
Pulmonary complications of sickle cell disease: a narrative clinical review.
Pulmonary hypertension in chronic hemolytic anemias: Pathophysiology and treatment.
Pulmonary hypertension in sickle cell disease.
Pulmonary hypertension in sickle cell disease: diagnosis and management.
Redox-dependent impairment of vascular function in sickle cell disease.
Review: Hemodynamic Characteristics and Outcomes of Sickle Cell Disease Associated Pulmonary Hypertension.
Right ventricular and pulmonary function in sickle cell disease patients with pulmonary hypertension.
Role of the coagulation system in the pathogenesis of sickle cell disease.
Sickle cell disease and H3Africa: enhancing genomic research on cardiovascular diseases in African patients.
Sickle cell disease and pulmonary hypertension in Africa: a global perspective and review of epidemiology, pathophysiology, and management.
Sickle cell disease and venous thromboembolism: what the anticoagulation expert needs to know.
Sickle cell disease as a vascular disorder.
Sickle cell disease related chronic thromboembolic pulmonary hypertension: challenging clinical scenario.
Sickle cell disease: at the crossroads of pulmonary hypertension and diastolic heart failure.
Sickle cell leg ulcers: a frequently disabling complication and a marker of severity.
Sickle-cell anemia and pulmonary hypertension.
Smooth muscle cytochrome b5 reductase 3 deficiency accelerates pulmonary hypertension development in sickle cell mice.
Soluble CD163 in young sickle cell disease patients and their trait siblings: a biomarker for pulmonary hypertension and vaso-occlusive complications.
Soluble Fas/FasL ratio as a marker of vasculopathy in children and adolescents with sickle cell disease.
Thalassemia major and sickle cell disease in adolescents and young adults.
The different facets of sickle cell disease-related pulmonary hypertension.
The Economic Burden of End-Organ Damage Among Medicaid Patients with Sickle Cell Disease in the United States: A Population-Based Longitudinal Claims Study.
The role of the arginine metabolome in pain: implications for sickle cell disease.
The Worst Things in Life are Free: The Role of Free Heme in Sickle Cell Disease.
Tumor Necrosis Factor-Superfamily 15 Gene Expression in Patients with Sickle Cell Disease.
Vascular complications of sickle cell disease.
Young adults with SCD in US children's hospitals: Are they different from adolescents?
Hyperthyroidism
Population-based studies of antithyroid drugs and sudden cardiac death.
Hypertriglyceridemia
Altered metabolic responses to intermittent hypoxia in mice with partial deficiency of hypoxia-inducible factor-1alpha.
Cell type-dependent pro- and anti-inflammatory role of signal transducer and activator of transcription 3 in alcoholic liver injury.
Levels of high-density lipoprotein cholesterol (HDL-C) among children with steady-state sickle cell disease.
Low birth weight causes insulin resistance and aberrant intestinal lipid metabolism independent of microbiota abundance in Landrace-Large White pigs.
Relationship between stearoyl-CoA desaturase activity and plasma triglycerides in human and mouse hypertriglyceridemia.
Stearoyl-coenzyme A desaturase 1 deficiency protects against hypertriglyceridemia and increases plasma high-density lipoprotein cholesterol induced by liver X receptor activation.
Hypertrophy, Left Ventricular
A validation study of the European Society of Cardiology guidelines for risk stratification of sudden cardiac death in childhood hypertrophic cardiomyopathy.
Acute restraint stress provokes sudden cardiac death in normotensive rats and enhances susceptibility to arrhythmogenic effects of adrenaline in spontaneously hypertensive rats.
Antihypertensive therapy and sudden cardiac death, should we expect the unexpected?
Association between Clinical and Doppler Echocardiographic Parameters with Sudden Death in Hemodialysis Patients.
Atrial fibrillation and its association with sudden cardiac death.
Comparison of biventricular dimensions and function between pediatric sickle-cell disease and thalassemia major patients without cardiac iron.
Coronary Artery Dilation in Sickle Cell Disease.
Diastolic dysfunction in sickle cell.
Early Repolarization Pattern and Left Ventricular Mass in Hypertrophic Cardiomyopathy.
Electrocardiogram as a predictor of sudden cardiac death in middle-aged subjects without a known cardiac disease.
Electrocardiographic predictors of mortality and sudden cardiac death in patients with end stage renal disease on hemodialysis.
Evaluation of left ventricular diastolic function in pediatric sickle cell disease patients.
Hypertension Is a Risk Factor for Several Types of Heart Disease: Review of Prospective Studies.
Hypertrophic cardiomyopathy: Can the noninvasive diagnostic testing identify high risk patients?
Inducibility of life-threatening ventricular arrhythmias is related to maximum left ventricular thickness and clinical markers of sudden cardiac death in patients with hypertrophic cardiomyopathy attributable to the Asp175Asn mutation in the alpha-tropomyosin gene.
Loss of stearoyl-CoA desaturase 1 rescues cardiac function in obese leptin deficient mice.
Predicting sudden cardiac death in a general population using an electrocardiographic risk score.
Predictors of sudden cardiac death in atrial fibrillation: The Atherosclerosis Risk in Communities (ARIC) study.
Prognostic significance of beta-myosin heavy chain mutations is reflective of their hypertrophic expressivity in patients with hypertrophic cardiomyopathy.
QRS duration predicts sudden cardiac death in hypertensive patients undergoing intensive medical therapy: the LIFE study.
Racial differences in sudden cardiac death among hypertensive patients during antihypertensive therapy: The LIFE study.
Rate-dependent electrical, contractile and restitution properties of isolated left ventricular myocytes in guinea-pig hypertrophy.
Relation of systemic blood pressure to sudden cardiac death.
Relationship of Sudden Cardiac Death to New-Onset Atrial Fibrillation in Hypertensive Patients with Left Ventricular Hypertrophy.
Risk stratification for sudden cardiac death in hypertrophic cardiomyopathy: systematic review of clinical risk markers.
Risk stratification in pediatric hypertrophic cardiomyopathy: Insights for bridging the evidence gap?
Structural pathways and prevention of heart failure and sudden death.
Subclinical Cardiac Dysfunction Is Associated With Extracardiac Organ Damages.
Sudden Cardiac Death Among Firefighters ?45 Years of Age in the United States.
Sudden cardiac death in asymptomatic patients with aortic stenosis.
Sudden Cardiac Death in Hypertensive Patients.
Sudden Cardiac Death in Patients With Atrial Fibrillation: Insights From the ENGAGE AF-TIMI 48 Trial.
Sudden Cardiac Death in Women.
Targeted molecular genetic testing in young sudden cardiac death victims from Western Denmark.
The 12-lead electrocardiogram of the elite female footballer as defined by different interpretation criteria across the competitive season.
The role of magnetic resonance imaging in hypertrophic cardiomyopathy.
The worsening of left ventricular hypertrophy is the strongest predictor of sudden cardiac death in haemodialysis patients: a 10 year survey.
Ventricular arrhythmia and sudden cardiac death in Fabry disease: a systematic review of risk factors in clinical practice.
Wide QRS-T Angle on the 12-Lead ECG as a Predictor of Sudden Death Beyond the LV Ejection Fraction.
Hyperventilation
Electroencephalography hyperventilation and stroke in children with sickle cell disease.
Hypesthesia
Clinical and MRI Differences Between Patients With Subacute Combined Degeneration of the Spinal Cord Related vs. Unrelated to Recreational Nitrous Oxide Use: A Retrospective Study.
Sensory and Thermal Quantitative Testing in Children With Sickle Cell Disease.
Subacute Combined Degeneration: A Retrospective Study of 68 Cases with Short-Term Follow-Up.
Hyphema
Treatment of post-traumatic trabecular mashwork thrombosis and secondary glaucoma with intracameral tissue plasminogen activator in previously unrecognized sickle cell anemia.
Hypoglycemia
Carnitine transport by organic cation transporters and systemic carnitine deficiency.
Liver gene expression analysis reveals endoplasmic reticulum stress and metabolic dysfunction in SCD1-deficient mice fed a very low-fat diet.
[Sudden cardiac death in diabetes mellitus].
Hypogonadism
Adverse effects of a clinically relevant dose of hydroxyurea used for the treatment of sickle cell disease on male fertility endpoints.
Compensated hypogonadism in men with sickle cell disease.
Hypogonadism in patients with sickle cell disease: central or peripheral?.
Impaired pubertal development and testicular hormone function in males with sickle cell anemia.
Male sickle cell patients, compensated transpubertal hypogonadism and normal final growth.
Statural Growth and Prevalence of Endocrinopathies in Relation to Liver Iron Content (LIC) in Adult Patients with Beta Thalassemia Major (BTM) and Sickle Cell Disease (SCD).
Testosterone replacement therapy does not promote priapism in hypogonadal men with sickle cell disease: 12-month safety report.
Trace elements in sickle cell disease.
TSPO ligand FGIN-1-27 controls priapism in sickle cell mice via endogenous testosterone production.
Hypokalemia
Aborted sudden cardiac death in two patients with Bartter's/Gitelman's syndromes.
Combined effect of renal function and serum potassium level in sudden cardiac death in aging hypertensive subjects.
Recurrent aborted sudden cardiac death with seizures and rhabdomyolysis due to bulimia-induced hypokalemia: report of one case.
Hypopigmentation
Severity in phenotypic expression of homozygous sickle cell disease (Hb.SS) - Does hypermelanotic or hypomelanotic skin status of affected patients play a role?
Hypotension
Nonpneumatic Anti-Shock Garment versus Intermittent Sequential Compression Device for Prevention of Postspinal Hypotension in Patients Undergoing Cesarean Section: A Randomized Controlled Study.
The effect of a sequential compression device on hemodynamics in arthroscopic shoulder surgery using beach-chair position.
The effect of sequential compression device on hypotension in the sitting position during shoulder arthroscopy; a comparison with elastic stocking.
The Intermittent Sequential Compression Device on the Lower Extremities Attenuates the Decrease in Regional Cerebral Oxygen Saturation During Sitting Position Under Sevoflurane Anesthesia.
Hypotension, Orthostatic
[A multivariate analysis of prognostic factors of spinocerebellar degenerations]
Hypothyroidism
Fracture prevalence and relationship to endocrinopathy in iron overloaded patients with sickle cell disease and thalassemia.
Statural Growth and Prevalence of Endocrinopathies in Relation to Liver Iron Content (LIC) in Adult Patients with Beta Thalassemia Major (BTM) and Sickle Cell Disease (SCD).
Thyroid Function 'in Egyptian Children with Sickle Cell Anemia in correlation with iron' load.
Thyroid hemodynamic alterations in Egyptian patients with sickle cell disease: relation to disease severity, total body iron and thyroid function.
Hypoxia, Brain
Cerebral oximetry improves detection of sickle cell patients at risk for nocturnal cerebral hypoxia.
Ileus
Laparoscopic splenic procedures in children: experience in 231 children.
Infant, Newborn, Diseases
Description of criteria for near miss in high-complexity obstetric population with sickle cell anemia: an observational study.
Infarction, Middle Cerebral Artery
mTOR Inhibition Improves Anaemia and Reduces Organ Damage in a Murine Model of Sickle Cell Disease.
Infections
A Meta-Analysis on the Seroprevalence of Parvovirus B19 among Patients with Sickle Cell Disease.
Abdominal pain in children with sickle cell disease.
Acute chest syndrome in sickle cell disease.
Age-Related Emergency Department Reliance in Patients with Sickle Cell Disease.
Alteration of humoral, cellular and cytokine immune response to inactivated influenza vaccine in patients with Sickle Cell Disease.
AMPK? pathway involved in hepatic triglyceride metabolism disorder in diet-induced obesity mice following Escherichia coli Infection.
Analysis of Causes of Hospitalization Among Children with Sickle Cell Disease in a Group of Private Hospitals in Jeddah, Saudi Arabia.
Assessing the Immunogenic Response of a Single Center's Pneumococcal Vaccination Protocol in Sickle Cell Disease.
Association of HIV infection with clinical and laboratory characteristics of sickle cell disease.
Asymptomatic malaria parasitaemia in sickle-cell disease patients: how effective is chemoprophylaxis?
Bartonella henselae Infection in Sickle Cell Disease Mice Is Associated with Hyperalgesia.
Bordetella holmesii bacteremia in sickle cell disease.
Brugada Syndrome: The Role of Risk Stratification in Selecting Patients for Implantable Cardioverter-defibrillator Placement.
Causes of hospitalization in sickle cell diseased children in western region of Saudi Arabia. A single center study.
Central venous catheter complications in sickle cell disease.
Children with sickle cell disease and human immunodeficiency virus-1 infection: use of inpatient care services in the United States.
COVID-19 and Sickle Cell Disease in Bahrain.
Curing Hemoglobinopathies: Challenges and Advances of Conventional and New Gene Therapy Approaches.
Diminished antibody response to hepatitis B immunization in children with sickle cell disease.
Dual kidney transplants from very old or very young donors: long-term outcomes and complications.
Effect of zinc supplementation on incidence of infections and hospital admissions in sickle cell disease (SCD).
Effects of adenoviral gene transfer of C. elegans n-3 fatty acid desaturase on the lipid profile and growth of human breast cancer cells.
Effects of vaccines in patients with sickle cell disease: a systematic review protocol.
Epidemiology and treatment of relative anemia in children with sickle cell disease in sub-Saharan Africa.
Epidemiology of Bloodstream Infections in Children with Sickle Cell Disease.
Epidemiology of human parvovirus B19 in children with sickle cell disease.
Fever in sickle cell disease patients in the Kingdom of Bahrain.
Fever Management in Sickle Cell Disease in Low- and Middle-Income Countries: A Survey of SCD Management Programs.
Frequency of bacteremia in patients with sickle cell disease: a longitudinal study.
Functional study of Capsicum annuum fatty acid desaturase 1 cDNA clone induced by Tobacco mosaic virus via microarray and virus-induced gene silencing.
Genome-wide evaluation of the interplay between Caenorhabditis elegans and Yersinia pseudotuberculosis during in vivo biofilm formation.
Health policy for sickle cell disease in Africa: experience from Tanzania on interventions to reduce under-five mortality.
Helicobacter pylori infection among a pediatric population with sickle cell disease.
Helicobacter pylori infection in sickle cell disease.
Hemoglobinopathy and pediatrics in the time of COVID-19.
Hepatitis B and C viral markers in patients with sickle cell disease in Ibadan, Nigeria.
High frequency of the CCR5delta32 variant among individuals from an admixed Brazilian population with sickle cell anemia.
HLA-G polymorphism influences the susceptibility to HCV infection in sickle cell disease patients.
How we prevent and manage infection in sickle cell disease.
Imaging review of sickle cell disease for the emergency radiologist.
Impact of Mannose-Binding Protein Gene Polymorphisms in Omani Sickle Cell Disease Patients.
Implications of COVID-19 infections in sickle cell disease.
Improvement of maternal and fetal outcomes in women with sickle cell disease treated with early prophylactic erythrocytapheresis.
In vitro lymphocyte blastogenic responses and cytokine production in sickle cell disease patients with acute pneumonia.
In vivo production of type 1 cytokines in healthy sickle cell disease patients.
Inadequate community knowledge about sickle cell disease among African-American women.
Incidence and predictors of sudden cardiac death after heart transplantation: A systematic review and meta-analysis.
Incidence of invasive Haemophilus influenzae infections in children with sickle cell disease.
Increased iron export by ferroportin induces restriction of HIV-1 infection in sickle cell disease.
Infection in sickle cell disease: A review.
Infections and immunizations of children with sickle cell disease.
Infections and sickle cell disease in Eastern Saudi Arabian children.
Infections in sickle cell anemia: pathogenesis and control.
Infections in thalassemia and hemoglobinopathies: focus on therapy-related complications.
Infectious complications in sickle cell disease are influenced by HLA class II alleles.
Inflammatory Dendritic Cells Contribute to Regulate the Immune Response in Sickle Cell Disease.
Influenza Vaccination Protects Against Pandemic H1N1 Infection in Sickle Cell Disease Mice.
Influenza vaccine effectiveness and disease burden in children and adolescents with sickle cell disease: 2012-2017.
Innate immune defense defines susceptibility of sarcoma cells to measles vaccine virus-based oncolysis.
Interferon production in sickle cell disease.
Investigational selectin-targeted therapy of sickle cell disease.
Is Chlamydia pneumoniae infection associated with stroke in children with sickle cell disease?
Is sickle cell disease a risk factor for severe COVID-19 outcomes in hospitalized patients? A multicenter national retrospective cohort study.
Knowledge and Health Beliefs Regarding Sickle Cell Disease Among Omanis in a Primary Healthcare Setting: Cross-sectional study.
Knowledge, attitudes and beliefs of primary caretakers towards sickle cell anaemia in children.
Life threatening parvovirus B19 and herpes simplex virus associated acute myocardial dysfunction in a child with homozygous sickle cell disease.
Life-Threatening Infectious Complications in Sickle Cell Disease: A Concise Narrative Review.
Long-term central venous access in patients with sickle cell disease. Incidence of thrombotic and infectious complications.
Low rates of transfusion-transmitted infection screening in chronically transfused adults with sickle cell disease.
Lymphocyte blastogenic responses in sickle cell disease.
Malaria as a cause of morbidity and mortality in children with homozygous sickle cell disease on the coast of Kenya.
Malaria in patients with sickle cell anaemia: burden, risk factors and outcome at the Laquintinie hospital, Cameroon.
Management of a broken modular femoral stem following total hip arthroplasty in a patient with sickle cell disease using an endofemoral trephine reamer: A case report.
Management of Sickle Cell Disease in Children.
Micronutrients and sickle cell disease, effects on growth, infection and vaso-occlusive crisis: a systematic review.
Morbidity associated with sickle cell disease in pregnancy.
Mortality among children with sickle cell disease identified by newborn screening during 1990-1994--California, Illinois, and New York.
Multimodality Treatment for Nonhealing Wound With Osteomyelitis in Sickle Cell Disease.
Multiple bone and joint diseases in a nigerian sickle cell anaemia: a case report.
Neutrophil dysfunctions in sickle cell disease.
Older red cell units are associated with an increased incidence of infection in chronically transfused adults with sickle cell disease.
Opioids are not a major cause of death of patients with sickle cell disease.
Parvovirus B19 infection in children with sickle cell disease in the hydroxyurea era.
Parvovirus B19 infection in sickle cell disease: An analysis from the Centers for Disease Control haemoglobinopathy blood surveillance project.
Peg-interfon alpha-2a and low-dose ribavirin for treatment of hepatitis C virus infection in patients with sickle-cell anemia in Saudi Arabia.
Penicillin- and cephalosporin-resistant strains of Streptococcus pneumoniae causing sepsis and meningitis in children with sickle cell disease.
Perioperative Management of Sickle Cell Disease.
Placenta growth factor activates monocytes and correlates with sickle cell disease severity.
Poor Long-Term Efficacy of Prevnar-13 in Sickle Cell Disease Mice Is Associated with an Inability to Sustain Pneumococcal-Specific Antibody Titers.
Pregnancy in patients with sickle cell disease: maternal and perinatal outcomes.
Pregnancy Outcomes among Patients with Sickle Cell Disease in Brazzaville.
Prevalence and Factors Associated with Human Parvovirus B19 Infection in Sickle Cell Patients Hospitalized in Tanzania.
Prevalence and factors associated with renal dysfunction in children admitted to two hospitals in northwestern Tanzania.
Prevalence of Bacteremia in Febrile Patients With Sickle Cell Disease: Meta-Analysis of Observational Studies.
Prevalence of Hepatitis B, Hepatitis C, and HIV in Multiply Transfused Sickle Cell Disease Patients from Oman.
Prevalence of Hepatitis C among Egyptian Children with Sickle Cell Disease and the Role of IL28b Gene Polymorphisms in Spontaneous Viral Clearance.
Prevalence of Plasmodium falciparum and non-P. falciparum infections in a highland district in Ghana, and the influence of HIV and sickle cell disease.
Preventing Infections in Sickle Cell Disease: The Unfinished Business.
Prophylactic antibiotics for preventing pneumococcal infection in children with sickle cell disease.
PspA family typing and PCR-based DNA fingerprinting with BOX A1R primer of pneumococci from the blood of patients in the USA with and without sickle cell disease.
Psychiatric diagnosis in adolescents with sickle cell disease: a preliminary report.
Public health impact of daily life triggers of sudden cardiac death: A systematic review and comparative risk assessment.
Quantitative Assessment of Ciliary Ultrastructure with the Use of Automatic Analysis: PCD Quant.
Reduced levels of CD2+ cells and T-cell subsets in patients with sickle cell anaemia.
Respiratory syncytial virus and seasonal influenza cause similar illnesses in children with sickle cell disease.
Restriction of HIV-1 Infection in Sickle Cell Trait.
Risk of Asymptomatic Bacteriuria among People with Sickle Cell Disease in Accra, Ghana.
Risk of Invasive Pneumococcal Disease in Children with Sickle Cell Disease in England: A National Observational Cohort Study, 2010-2015.
Robust adaptive immune response against Babesia microti infection marked by low parasitemia in a murine model of sickle cell disease.
Saccharomyces cerevisiae-derived virus-like particle parvovirus B19 vaccine elicits binding and neutralizing antibodies in a mouse model for sickle cell disease.
Salmonella as a causative organism of various infections in patients with sickle cell disease.
Screening for sickle cell disease in newborns: a systematic review.
Septic complications after splenectomy for sickle cell sequestration crisis.
Serum alpha-hydroxybutyrate dehydrogenase levels in children with sickle cell disease.
Severe COVID-19 with acute respiratory distress syndrome (ARDS) in a sickle cell disease adult patient: case report.
Severe hemolysis and vaso-occlusive crisis due to COVID-19 infection in a sickle cell disease patient improved after red blood cell exchange.
Severe infection including disseminated herpes zoster triggered by subclinical Cushing's disease: a case report.
Severe oxidative stress in sickle cell disease patients with uncomplicated Plasmodium falciparum malaria in Kampala, Uganda.
Severe pneumococcal sepsis and meningitis in human immunodeficiency virus-infected adults with sickle cell disease.
Severity of Salmonella infection among sickle cell diseases pediatric patients: Description of the infection pattern.
Sickle cell anemia in the pediatric intensive care unit: novel approaches for managing life-threatening complications.
Sickle Cell Disease and Infections in High- and Low-Income Countries.
Sickle cell disease and malaria: decreased exposure and asplenia can modulate the risk from Plasmodium falciparum.
Sickle cell disease in pregnancy: maternal complications in a medicaid-enrolled population.
Sickle cell disease in pregnancy: trend and pregnancy outcomes at a tertiary hospital in Tanzania.
Sickle cell disease subphenotypes in patients from southwestern province of saudi arabia.
Sickle cell disease: Classification of clinical complications and approaches to preventive and therapeutic management.
Sickle cell disease: current clinical management.
Sickle cell disease: management options and challenges in developing countries.
Sickle cell disease: the need for a public health agenda.
Sickle cell disease: two fatalities due to bone marrow emboli in patients with acute chest syndrome.
Sickle-cell disease in febrile children living in a rural village of Madagascar and association with malaria and respiratory infections.
Simultaneous acute splenic sequestration and transient aplastic crisis in children with sickle cell disease.
Splenic sepsis in sickle cell disease.
Stearoyl-CoA Desaturase-Mediated Monounsaturated Fatty Acid Availability Supports Humoral Immunity.
Sterile subperiosteal fluid collections accompanying orbital wall infarction in sickle-cell disease.
Streptococcus pneumoniae and Its Virulence Factors H2O2 and Pneumolysin Are Potent Mediators of the Acute Chest Syndrome in Sickle Cell Disease.
Study of hepatic functions and prevalence of hepatitis-B surface antigenaemia in Omani children with sickle cell disease.
Subcutaneous implantable cardioverter defibrillator in cardiomyopathies and channelopathies.
Superimposed Hepatitis C Virus in Sickle Cell Disease Pregnant Woman.
Survival of children with sickle cell disease.
Suspected Severe Malaria in a Sudanese Patient Affected by Sickle Cell Disease Who Was Treated with Hydroxyurea.
Systemic lupus erythematosus in patients with sickle cell disease.
Systemic T Cell Subsets and Cytokines in Patients With Homozygous Sickle Cell Disease and Asymptomatic Urinary Tract Infections in Togo.
Technetium-99m-dimercaptosuccinic acid renal scintigraphy and single photon emission computed tomography/computed tomography in patients with sickle cell disease.
The burden of respiratory syncytial virus infections among children with sickle cell disease.
The impact of the 2009 H1N1 influenza pandemic on pediatric patients with sickle cell disease.
The radiological manifestations of sickle cell disease.
The role of infection in the pathogenesis of vaso-occlusive crisis in patients with sickle cell disease.
The Role of Inflammation and Leukocytes in the Pathogenesis of Sickle Cell Disease.
The Role of Inflammation and Leukocytes in the Pathogenesis of Sickle Cell Disease; Haemoglobinopathy.
The role of religious leaders and faith organisations in haemoglobinopathies: a review.
Total Hip Arthroplasty in Patients With Sickle Cell Disease: A Comprehensive Systematic Review.
Totally implantable intravenous catheters in the management of sickle cell anemia.
Transmission transmissible hepatitis B virus markers of infection among sickle cell disease patients receiving care at a tertiary health facility in Ibadan, southwest Nigeria.
Tuberculosis in adult patients with sickle cell disease.
Tumor necrosis factor alpha in children with sickle cell disease in stable condition.
Turf wars: exploring splenomegaly in sickle cell disease in malaria-endemic regions.
Urinary Bladder Dysfunction in Transgenic Sickle Cell Disease Mice.
Vascular Permeability Drives Susceptibility to Influenza Infection in a Murine Model of Sickle Cell Disease.
Vaso-occlusive crisis-associated neutrophil dysfunction in patients with sickle-cell disease.
Viral Ecogenomics of Arctic Cryopeg Brine and Sea Ice.
Viral metagenomics in Brazilian multiply transfused patients with sickle cell disease as an indicator for blood transfusion safety.
Vitamin D deficiency is associated with sudden cardiac death, combined cardiovascular events, and mortality in haemodialysis patients.
Wasting and Sudden Cardiac Death in Hemodialysis Patients: A Post Hoc Analysis of 4D (Die Deutsche Diabetes Dialyse Studie).
White blood cell count as a predictor of the severity of sickle cell disease during pregnancy.
White Paper: Pathways to Progress in Newborn Screening for Sickle Cell Disease in Sub-Saharan Africa.
Zinc supplementation decreases oxidative stress, incidence of infection, and generation of inflammatory cytokines in sickle cell disease patients.
[Cardiac complications of sickle cell disease in children].
[Human immunodeficiency virus, hepatitis C virus and hepatitis B viruses in patients with sickle-cell disease in Togo]
[Human parvovirus B19 infection in sickle cell disease patients. A two siblings report].
[Infections in Senegalese children and adolescents with sickle cell anemia: epidemiological aspects]
[Infectious complications after surgical splenectomy in children with sickle cell anemia disease].
[Wearable cardioverter-defibrillators: clinical experience and future perspectives].
Infertility
Assessment of density gradient centrifugation (DGC) and sperm chromatin dispersion (SCD) measurements in couples with male factor infertility undergoing ICSI.
Comprehensive analysis of sperm DNA fragmentation by five different assays: TUNEL assay, SCSA, SCD test and alkaline and neutral Comet assay.
Desire for parenthood and reproductive health knowledge in adolescents and young adults with sickle cell disease and their caregivers.
Diagnostic Accuracies of the TUNEL, SCD, and Comet Based Sperm DNA Fragmentation Assays for Male Infertility: a Meta-analysis Study.
Diagnostic accuracy of sperm DNA degradation index (DDSi) as a potential noninvasive biomarker to identify men with varicocele-associated infertility.
Fertility challenges for women with sickle cell disease.
Fertility Concerns and Access to Care for Stem Cell Transplantation Candidates with Sickle Cell Disease.
Increased sperm chromatin decondensation in selected nonapoptotic spermatozoa of patients with male infertility.
Preimplantation genetic diagnosis in an HIV-serodiscordant couple carrier for sickle cell disease: lessons from a case report.
Reproductive issues in sickle cell disease.
Sperm chromatin structure assay versus sperm chromatin dispersion kits: Technical repeatability and choice of assisted reproductive technology procedure.
The opinion of caregivers on aspects of schizophrenia and major affective disorders in a Nigerian setting.
The sperm chromatin dispersion test: a simple method for the determination of sperm DNA fragmentation.
Infertility, Male
Comprehensive analysis of sperm DNA fragmentation by five different assays: TUNEL assay, SCSA, SCD test and alkaline and neutral Comet assay.
Diagnostic Accuracies of the TUNEL, SCD, and Comet Based Sperm DNA Fragmentation Assays for Male Infertility: a Meta-analysis Study.
Evaluation of sperm DNA fragmentation using multiple methods: a comparison of their predictive power for male infertility.
Seminal parameters of ejaculates collected from oligospermic and normospermic patients via masturbation and at intercourse with the use of a Silastic seminal fluid collection device.
Inflammatory Bowel Diseases
Deficiency of Stearoyl-CoA Desaturase-1 Aggravates Colitogenic Potential of Adoptively Transferred Effector T cells.
Gangrene of the digits of the right lower limb in a patient with homozygous sickle cell disease and ulcerative colitis.
Is there an added value of faecal calprotectin and haemoglobin in the diagnostic work-up for primary care patients suspected of significant colorectal disease? A cross-sectional diagnostic study.
Influenza, Human
Alteration of humoral, cellular and cytokine immune response to inactivated influenza vaccine in patients with Sickle Cell Disease.
Ambulatory quality indicators to prevent infection in sickle cell disease.
Burden of influenza-related hospitalizations among children with sickle cell disease.
Influenza vaccination rates and hospitalizations among Medicaid enrollees with and without sickle cell disease, 2009-2015.
Influenza vaccine effectiveness and disease burden in children and adolescents with sickle cell disease: 2012-2017.
Inhibition of Stearoyl-CoA desaturases suppresses follicular help T and germinal center B cell responses.
Maintenance of a High Influenza Vaccination Rate and Improvement in Health Outcomes in a Pediatric Sickle Cell Disease Clinic.
Preventive Care Delivery to Young Children With Sickle Cell Disease.
Public health impact of daily life triggers of sudden cardiac death: A systematic review and comparative risk assessment.
Respiratory syncytial virus and seasonal influenza cause similar illnesses in children with sickle cell disease.
Severe pandemic H1N1 and seasonal influenza in children and young adults with sickle cell disease.
Significance of electronic health records: A comparative study of vaccination rates in patients with sickle cell disease.
Stearoyl-CoA Desaturase-Mediated Monounsaturated Fatty Acid Availability Supports Humoral Immunity.
The impact of the 2009 H1N1 influenza pandemic on pediatric patients with sickle cell disease.
Vascular Permeability Drives Susceptibility to Influenza Infection in a Murine Model of Sickle Cell Disease.
Insulin Resistance
A novel inhibitor of stearoyl-CoA desaturase-1 attenuates hepatic lipid accumulation, liver injury and inflammation in model of nonalcoholic steatohepatitis.
Abdominal adiposity is associated with fatty acid desaturase activity in boys: Implications for C-reactive protein and insulin resistance.
Adipose-specific deletion of stearoyl-CoA desaturase 1 up-regulates the glucose transporter GLUT1 in adipose tissue.
Analysis of the contribution to type 2 diabetes susceptibility of sequence variation in the gene encoding stearoyl-CoA desaturase, a key regulator of lipid and carbohydrate metabolism.
Association of Changes in Body Fatness and Fatty Acid Composition of Plasma Phospholipids During Early Puberty in Japanese Children.
Associations between estimated fatty acid desaturase activities in serum lipids and adipose tissue in humans: links to obesity and insulin resistance.
Atypical antipsychotic medications increase postprandial triglyceride and glucose levels in male rats: Relationship with stearoyl-CoA desaturase activity.
Biochemical and Physiological Function of Stearoyl-CoA Desaturase.
Clinical Overview of Obesity and Diabetes Mellitus as Risk Factors for Atrial Fibrillation and Sudden Cardiac Death.
Corn oil versus lard: Metabolic effects of omega-3 fatty acids in mice fed obesogenic diets with different fatty acid composition.
Critical role of stearoyl-CoA desaturase-1 (SCD1) in the onset of diet-induced hepatic insulin resistance.
De novo lipogenesis and stearoyl-CoA desaturase are coordinately regulated in the human adipocyte and protect against palmitate-induced cell injury.
Despite antiatherogenic metabolic characteristics, SCD1-deficient mice have increased inflammation and atherosclerosis.
Down-regulation of hepatic stearoyl-CoA desaturase 1 expression by angiotensin II receptor blocker in the obese fa/fa Zucker rat: possible role in amelioration of insulin resistance and hepatic steatosis.
Effects of four-week high-fructose diet on gene expression in skeletal muscle of healthy men.
Effects of gender and GH secretory pattern on sterol regulatory element-binding protein-1c and its target genes in rat liver.
Effects of insulin on glucose uptake and leg blood flow in patients with sickle cell disease and normal subjects.
Effects of pioglitazone on stearoyl-CoA desaturase in obese Zucker fa/fa rats.
Endogenous ?-3 polyunsaturated fatty acid production confers resistance to obesity, dyslipidemia, and diabetes in mice.
Erratum to: Stearoyl CoA desaturase 1 is elevated in obesity but protects against fatty acid-induced skeletal muscle insulin resistance in vitro.
Fatty Acid Bile Acid Conjugate Inhibits Hepatic Stearoyl Coenzyme A Desaturase and Is Non-atherogenic.
Fatty acid desaturase (FADS) gene polymorphisms and insulin resistance in association with serum phospholipid polyunsaturated fatty acid composition in healthy Korean men: cross-sectional study.
Fatty Acid desaturase gene polymorphisms and metabolic measures in schizophrenia and bipolar patients taking antipsychotics.
Fatty acid desaturases in human adipose tissue: relationships between gene expression, desaturation indexes and insulin resistance.
Fatty acid desaturation index in human plasma: comparison of different analytical methodologies for the evaluation of diet effects.
Fatty Liver Is Associated with Transcriptional Downregulation of Stearoyl-CoA Desaturase and Impaired Protein Dimerization.
Fenretinide Induces Ubiquitin-Dependent Proteasomal Degradation of Stearoyl-CoA Desaturase in Human Retinal Pigment Epithelial Cells.
Gene expression profiling in skeletal muscle of Zucker diabetic fatty rats: implications for a role of stearoyl-CoA desaturase 1 in insulin resistance.
Gene Expression Signature in Adipose Tissue of Acromegaly Patients.
Genome-Wide Association Studies of Estimated Fatty Acid Desaturase Activity in Serum and Adipose Tissue in Elderly Individuals: Associations with Insulin Sensitivity.
GLP-1 Elicits an Intrinsic Gut-Liver Metabolic Signal to Ameliorate Diet-Induced VLDL Overproduction and Insulin Resistance.
Glucose oversupply increases Delta9-desaturase expression and its metabolites in rat skeletal muscle.
Hepatocyte differentiation of human induced pluripotent stem cells is modulated by stearoyl-CoA desaturase 1 activity.
Improvements in glucose tolerance and insulin sensitivity after lifestyle intervention are related to changes in serum fatty acid profile and desaturase activities: the SLIM study.
Inactivity-mediated insulin resistance is associated with upregulated pro-inflammatory fatty acids in human cell membranes.
Increased Stearoyl-CoA Desaturase Index and Triglyceride Content in the Liver of Rats after a Single Bout of Swimming Exercise.
Indices of fatty acid desaturase activity in healthy human subjects: effects of different types of dietary fat.
Individual stearoyl-coa desaturase 1 expression modulates endoplasmic reticulum stress and inflammation in human myotubes and is associated with skeletal muscle lipid storage and insulin sensitivity in vivo.
Inhibition of stearoyl-coenzyme A desaturase 1 dissociates insulin resistance and obesity from atherosclerosis.
Longitudinal associations of serum fatty acid composition with type 2 diabetes risk and markers of insulin secretion and sensitivity in the Finnish Diabetes Prevention Study.
Loss of stearoyl-CoA desaturase-1 improves insulin sensitivity in lean mice but worsens diabetes in leptin-deficient obese mice.
Low hepatic stearoyl-CoA desaturase 1 activity is associated with fatty liver and insulin resistance in obese humans.
Lower estimates of delta-5 desaturase and elongase activity are related to adverse profiles for several metabolic risk factors in young Japanese women.
Meta-analysis approach identifies candidate genes and associated molecular networks for type-2 diabetes mellitus.
Metformin Inhibits Nuclear Receptor TR4-Mediated Hepatic Stearoyl-Coenzyme A Desaturase 1 Gene Expression With Altered Insulin Sensitivity.
Monounsaturated fatty acids generated via stearoyl CoA desaturase-1 are endogenous inhibitors of fatty acid amide hydrolase.
Opposite relationship between circulating soluble CD14 concentration and endothelial function in diabetic and nondiabetic subjects.
Peroxisome proliferator-activated receptor-? agonists have opposing effects on insulin resistance in high fat fed rats and mice due to different metabolic responses in muscle.
Pharmacological inhibition of Stearoyl-CoA Desaturase 1 improves insulin sensitivity in insulin-resistant rat models.
Physiological concentrations of insulin and T3 stimulate 3T3-L1 adipocyte acyl-CoA synthetase gene transcription.
Polymorphisms in Fatty Acid Desaturase (FADS) Gene Cluster: Effects on Glycemic Controls Following an Omega-3 Polyunsaturated Fatty Acids (PUFA) Supplementation.
Polymorphisms in the SCD1 gene: associations with body fat distribution and insulin sensitivity.
Probing the role of stearoyl-CoA desaturase-1 in hepatic insulin resistance.
Prominent role of liver in elevated plasma palmitoleate levels in response to rosiglitazone in mice fed high-fat diet.
Reduced expression of stearoyl-CoA desaturase-1, but not free fatty acid receptor 2 or 4 in subcutaneous adipose tissue of patients with newly diagnosed type 2 diabetes mellitus.
Relationship between oxidative stress, ferritin and insulin resistance in sickle cell disease.
Role of hepatic desaturases in obesity-related metabolic disorders.
Role of stearoyl-coenzyme A desaturase in regulating lipid metabolism.
Rosiglitazone increases indexes of stearoyl-CoA desaturase activity in humans: link to insulin sensitization and the role of dominant-negative mutation in peroxisome proliferator-activated receptor-gamma.
Serum fatty acid composition and indices of stearoyl-CoA desaturase activity are associated with systemic inflammation : longitudinal analyses in middle-aged men.
Serum fatty acid composition and insulin resistance are independently associated with liver fat markers in elderly men.
SIRT3 Deficiency and Mitochondrial Protein Hyperacetylation Accelerate the Development of the Metabolic Syndrome.
Skeletal-Muscle Triglycerides, Diacylglycerols, and Ceramides in Insulin Resistance: Another Paradox in Endurance-Trained Athletes?
Stearoyl CoA Desaturase 1 and Inositol-Requiring Protein 1? Determine the Efficiency of Oleic Acid in Alleviating Silica Nanoparticle-Induced Insulin Resistance.
Stearoyl CoA desaturase 1 is elevated in obesity but protects against fatty acid-induced skeletal muscle insulin resistance in vitro.
Stearoyl-CoA desaturase - a new player in skeletal muscle metabolism regulation.
Stearoyl-CoA desaturase 1 deficiency elevates insulin-signaling components and down-regulates protein-tyrosine phosphatase 1B in muscle.
Stearoyl-CoA desaturase and insulin signaling - What is the molecular switch?
Stearoyl-CoA desaturase enzyme 1 inhibition reduces glucose utilization for de novo fatty acid synthesis and cell proliferation in 3T3-L1 adipocytes.
Stearoyl-CoA desaturase-1 deficiency attenuates obesity and insulin resistance in leptin-resistant obese mice.
Stearoyl-CoA Desaturase-1 Is Associated with Insulin Resistance in Morbidly Obese Subjects.
Stearoyl-CoA Desaturase: A Vital Checkpoint in the Development and Progression of Obesity.
Testosterone differentially regulates targets of lipid and glucose metabolism in liver, muscle and adipose tissues of the testicular feminised mouse.
The dual-specificity phosphatase 2 (DUSP2) does not regulate obesity-associated inflammation or insulin resistance in mice.
The fate and intermediary metabolism of stearic acid.
The Phospholipase C Inhibitor U73122 Attenuates trans-10, cis-12 Conjugated Linoleic Acid-Mediated Inflammatory Signaling and Insulin Resistance in Human Adipocytes.
The role of stearoyl-CoA desaturase in obesity, insulin resistance, and inflammation.
Triglyceride Paradox Is Related to Lipoprotein Size, Visceral Adiposity and Stearoyl-CoA Desaturase Activity in Black Versus White Women.
Vitamin A Improves Hyperglycemia and Glucose-Intolerance through Regulation of Intracellular Signaling Pathways and Glycogen Synthesis in WNIN/GR-Ob Obese Rat Model.
Intellectual Disability
Contribution of sickle cell disease to the occurrence of developmental disabilities: a population-based study.
Health status and healthcare use in a national sample of children with sickle cell disease.
Subtle brain abnormalities in children with sickle cell disease: relationship to blood hematocrit.
Intracranial Aneurysm
Cerebral haemorrhagic risk in children with sickle-cell disease.
Intracranial aneurysms in sickle cell disease: Aneurysms characteristics and modalities of endovascular approach to treat these patients.
Intracranial Aneurysms in Sickle-Cell Disease Are Associated With the Hemoglobin SS Genotype But Not With Moyamoya Syndrome.
Intracranial stenting as monotherapy in subarachnoid hemorrhage and sickle cell disease.
Treatment of a cerebral pial arteriovenous fistula in a patient with sickle cell disease-related moyamoya syndrome: case report.
Use of a flow-diverting stent for ruptured dissecting aneurysm treatment in a patient with sickle cell disease.
Intracranial Hemorrhages
Bleeding in patients with sickle cell disease: a population-based study.
Coexistent Sickle Cell Disease Has No Impact on the Safety or Outcome of Lytic Therapy in Acute Ischemic Stroke: Findings From Get With The Guidelines-Stroke.
Kidney Transplantation From a Donor With Sickle Cell Disease.
Nonaneurysmal Subarachnoid Hemorrhage in Sickle Cell Disease: Description of a Case and a Review of the Literature.
Primary hemorrhagic stroke in a 12-year-old female with sickle cell disease and normal transcranial Doppler.
Stroke prevention and treatment in sickle cell disease.
Intracranial Thrombosis
Thrombosis after kidney transplantation.
Iron Deficiencies
A history of repetitive cesarean section is a risk factor of anemia in healthy perimenopausal women: The Korea National Health and Nutrition Examination Survey 2010-2012.
Comparative Analysis of Iron Homeostasis in Sub-Saharan African Children with Sickle Cell Disease and Their Unaffected Siblings.
Iron deficiency in sickle cell anaemia.
Iron deficiency in Yemeni patients with sickle-cell disease.
Regulation of yeast fatty acid desaturase in response to iron deficiency.
Iron Overload
A pilot study of manual chronic partial exchange transfusion in children with sickle disease.
Absence of cardiac siderosis by MRI T2* despite transfusion burden, hepatic and serum iron overload in Lebanese patients with sickle cell disease.
American Society of Hematology 2020 guidelines for sickle cell disease: transfusion support.
APPROACHES TO TRANSFUSION THERAPY AND IRON OVERLOAD IN PATIENTS WITH SICKLE CELL DISEASE: Results of an International Survey.
Assessing cardiac and liver iron overload in chronically transfused patients with sickle cell disease.
Assessment of liver and cardiac iron overload using MRI in patients with chronic anemias in Latin American countries: results from ASIMILA study.
Bone mass density in adults with sickle cell disease.
Cardiac iron overload in sickle-cell disease.
Chronically Transfused Pediatric Sickle Cell Patients are Protected from Cardiac Iron Overload.
Clinical Predictive Value of Cystatin C in Pediatric Sickle Cell Disease: A Marker of Disease Severity and Subclinical Cardiovascular Dysfunction.
Consequences and management of iron overload in sickle cell disease.
Deferasirox for iron chelation in multitransfused children with sickle cell disease; long-term experience in the East London clinical haemoglobinopathy network.
Deferasirox for managing transfusional iron overload in people with sickle cell disease.
Deferiprone as an oral iron chelator in sickle cell disease.
Disparity in the management of iron overload between patients with sickle cell disease and thalassemia who received transfusions.
Effectiveness of Clinical Decision Support Based Intervention in the Improvement of Care for Adult Sickle Cell Disease Patients in Primary Care.
Excess heme upregulates heme oxygenase 1 and promotes cardiac ferroptosis in mice with sickle cell disease.
Health literacy and knowledge of chronic transfusion therapy in adolescents with sickle cell disease and caregivers.
Heme-bound iron activates placenta growth factor in erythroid cells via erythroid Krüppel-like factor.
Hidden brain iron content in sickle cell disease: impact on neurocognitive functions.
How we manage iron overload in sickle cell patients.
How we treat sickle hepatopathy and liver transplantation in adults.
Identification of hemochromatosis gene polymorphisms in chronically transfused patients with sickle cell disease.
Impact of long-term erythrocytapheresis on growth and peak height velocity of children with sickle cell disease.
Increased levels of soluble P-selectin correlate with iron overload in sickle cell disease.
Influence of iron regulating genes mutations on iron status in Egyptian patients with sickle cell disease.
Iron depletion: an ameliorating factor for sickle cell disease?
Iron metabolism and iron chelation in sickle cell disease.
Iron overload is a determinant of morbidity and mortality in adult patients with sickle cell disease.
Kidney iron deposition by R2* is associated with haemolysis and urinary iron.
Myocardial ischemia and right ventricular dysfunction in adult patients with sickle cell disease.
Non Transferrin Bound Labile Plasma Iron and Iron Overload in Sickle Cell Disease: a comparative study between Sickle Cell Disease and beta Thalassemic patients.
PATTERNS OF LIVER IRON ACCUMULATION IN SICKLE CELL DISEASE AND THALASSAEMIA PATIENTS WITH IRON OVERLOAD.
Pulmonary hypertension in sickle cell disease.
Recent advances in improving the management of sickle cell disease.
Red blood cell transfusion to treat or prevent complications in sickle cell disease: an overview of Cochrane reviews.
Reduced peripheral blood superoxide dismutase 2 expression in sickle cell disease.
Reduced vitamin E antioxidant capacity in sickle cell disease is related to transfusion status but not to sickle crisis.
Regulation of iron absorption in hemoglobinopathies.
Relationship between oxidative stress, ferritin and insulin resistance in sickle cell disease.
Safety and efficacy of high dose intravenous desferrioxamine for reduction of iron overload in sickle cell disease.
Selenium and Vitamin E as antioxidants in chronic hemolytic anemia: Are they deficient? A case-control study in a group of Egyptian children.
Serum apelin as a novel non-invasive marker for subclinical cardiopulmonary complications in children and adolescents with sickle cell disease.
Serum ferritin underestimates liver iron concentration in transfusion independent thalassemia patients as compared to regularly transfused thalassemia and sickle cell patients.
Serum Hepcidin Concentration in Individuals with Sickle Cell Anemia: Basis for the Dietary Recommendation of Iron.
Severe cardiac iron toxicity in two adults with sickle cell disease.
Shear dependent red blood cell adhesion in microscale flow.
Sickle cell disease: a review.
Sickle-cell nephropathy: MR imaging.
Soluble Fas/FasL ratio as a marker of vasculopathy in children and adolescents with sickle cell disease.
Soluble receptor for advanced glycation end products as a vasculopathy biomarker in sickle cell disease.
Stearoyl coenzyme A desaturase 1 expression and activity are increased in the liver during iron overload.
Study of Adrenal Functions using ACTH stimulation test in Egyptian children with Sickle Cell Anemia: Correlation with Iron Overload.
The Effect of Serum Ferritin Level on Gonadal, Prolactin, Thyroid Hormones, and Thyroid Stimulating Hormone in Adult Males with Sickle Cell Anemia.
The use of MRI to monitor iron overload in SCD.
Therapy insight: metabolic and endocrine disorders in sickle cell disease.
Thyroid Function 'in Egyptian Children with Sickle Cell Anemia in correlation with iron' load.
Thyroid hemodynamic alterations in Egyptian patients with sickle cell disease: relation to disease severity, total body iron and thyroid function.
Tissue Doppler Imaging-derived Diastolic Function Assessment in Children With Sickle Cell Disease and Its Relation With Ferritin.
Vitamin E correlates inversely with non-transferrin-bound iron in sickle cell disease.
Zinc mediates the SREBP-SCD axis to regulate lipid metabolism in Caenorhabditis elegans.
Ischemic Attack, Transient
Dynamic vascular analysis shows a hyperemic flow pattern in sickle cell disease.
Is Chlamydia pneumoniae infection associated with stroke in children with sickle cell disease?
Ischemic Stroke
Arteriopathy Influences Pediatric Ischemic Stroke Presentation, but Sickle Cell Disease Influences Stroke Management.
Association of HIV infection with clinical and laboratory characteristics of sickle cell disease.
Coexistent Sickle Cell Disease Has No Impact on the Safety or Outcome of Lytic Therapy in Acute Ischemic Stroke: Findings From Get With The Guidelines-Stroke.
Do chronic pain and comorbidities affect brain function in sickle cell patients? A systematic review of neuroimaging and treatment approaches.
Factor V Leiden G1691A and prothrombin G20210A mutations among Palestinian patients with sickle cell disease.
Patent foramen ovale in patients with sickle cell disease and stroke: case presentations and review of the literature.
Red blood cell mechanical sensitivity improves in patients with sickle cell disease undergoing chronic transfusion after prolonged, subhemolytic shear exposure.
Thrombolytic therapy for the treatment of acute ischaemic stroke in adults with homozygous sickle cell disease.
Transcranial Doppler Re-screening of Subjects who Participated in STOP and STOP II.
Treatment and prevention of stroke in children with sickle cell disease.
Jaundice, Neonatal
Jaundice in neonates with sickle cell disease. A case-control study.
The influence of infant and maternal sickle cell disease on birth outcome and neonatal course.
Jervell-Lange Nielsen Syndrome
Prevalence of Jervell-Lange Nielsen syndrome in children with congenital bilateral sensorineural hearing loss.
Joint Diseases
[Ultrasonographic evaluation of shoulder joints in hemodialysis patients]
Keratitis
Differential diagnosis of Schnyder corneal dystrophy.
kexin deficiency
Non-hematopoietic deficiency of proprotein convertase subtilisin/kexin type 9 deficiency leads to more severe anemia in a murine model of sickle cell disease.
Kidney Diseases
An Appraisal of Kidney Dysfunction and Its Risk Factors in Patients with Sickle Cell Disease.
Benefit of primary prevention implantable cardioverter-defibrillators in the setting of chronic kidney disease: a decision model analysis.
Chronic Disease Management in Sickle Cell Trait Patients in the Primary Care Setting: A Case Report.
Curing Hemoglobinopathies: Challenges and Advances of Conventional and New Gene Therapy Approaches.
Genetics of Sickle Cell-Associated Cardiovascular Disease: An Expert Review with Lessons Learned in Africa.
Lupus nephritis in a patient with sickle cell disease.
Renal replacement therapy in end-stage sickle cell nephropathy: presentation of two cases and literature review.
Sickle cell disease and H3Africa: enhancing genomic research on cardiovascular diseases in African patients.
Soluble Fas/FasL ratio as a marker of vasculopathy in children and adolescents with sickle cell disease.
Urinary transforming growth factor beta-1 as a marker of renal dysfunction in sickle cell disease.
Kidney Failure, Chronic
A Multi-Scale Investigation of Global Electrical Heterogeneity: Effects of Body Habitus, Respiration, and Tissue Conductivity.
Anaesthesia for renal transplantation in sickle cell disease.
Arrhythmias and Sudden Cardiac Death in End Stage Renal Disease: Epidemiology, Risk Factors, and Management.
Arrhythmic complication in cardiorenal syndrome.
Association of Abdominal Adiposity with Cardiovascular Mortality in Incident Hemodialysis.
Cardiac autonomic dysfunction in hemodialysis patients assessed by heart rate variability.
Chronic kidney disease and mortality in implantable cardioverter-defibrillator recipients.
Combination erythropoietin-hydroxyurea therapy in sickle cell disease: experience from the National Institutes of Health and a literature review.
Electrocardiographic predictors of mortality and sudden cardiac death in patients with end stage renal disease on hemodialysis.
End-Stage Renal Disease and Sudden Cardiac Death.
End-stage renal disease in patients with sickle cell disease.
Fludarabine-based nonmyeloablative stem cell transplantation for sickle cell disease with and without renal failure: clinical outcome and pharmacokinetics.
Heart rate variability (HRV) in kidney failure: measurement and consequences of reduced HRV.
High one year mortality in adults with sickle cell disease and end-stage renal disease.
Immunomodulatory Device Promotes a Shift of Circulating Monocytes to a Less Inflammatory Phenotype in Chronic Hemodialysis Patients.
Incidence of sudden cardiac death in adults with end-stage renal disease: a systematic review and meta-analysis.
Kidney transplant in a 26-year-old nigerian patient with sickle cell nephropathy.
Long-term outcomes of kidney transplantation from expanded criteria deceased donors at a single center: comparison with standard criteria deceased donors.
Long-term survival of implantable cardioverter defibrillator recipients with end-stage renal disease.
Management of the Dialysis Patient with Sickle Cell Disease.
Mild-to-moderate kidney dysfunction and the risk of sudden cardiac death in the setting of acute myocardial infarction.
Nephrin as a biomarker of sickle cell glomerulopathy in Malawi.
Outcomes of Kidney Transplant Recipients with Sickle Cell Disease: An Analysis of the 2000-2019 UNOS/OPTN Database.
Renal abnormalities in sickle cell disease.
Risk assessment for sudden cardiac death in dialysis patients: How relevant are conventional cardiac risk factors?
Risk of Sudden Cardiac Death in Chronic Kidney Disease.
Sudden cardiac death in CKD patients.
Sudden cardiac death in end stage renal disease: unlocking the mystery.
Survival and specific outcome of sickle cell disease patients after renal transplantation.
The Economic Burden of End-Organ Damage Among Medicaid Patients with Sickle Cell Disease in the United States: A Population-Based Longitudinal Claims Study.
The glomerulopathy of sickle cell disease.
The intuitive case for ?-blockers in patients with ESRD.
The kidney in sickle hemoglobinopathies?.
TpTe and TpTe/QT: novel markers to predict sudden cardiac death in ESRD?
[Spectrum of renal manifestations in sickle cell disease].
Kidney Neoplasms
Kidney cancer: Stearoyl-CoA desaturase: a novel therapeutic target for RCC.
Laminopathies
Case reports of a c.475G>T, p.E159* lamin A/C mutation with a family history of conduction disorder, dilated cardiomyopathy and sudden cardiac death.
Sudden cardiac death in neuromuscular disorders.
Language Development Disorders
A preliminary epidemiologic study of social (pragmatic) communication disorder in the context of developmental language disorder.
Language Disorders
A preliminary epidemiologic study of social (pragmatic) communication disorder in the context of developmental language disorder.
Learning Disabilities
Social communication disorder: a narrative review on current insights.
Leg Ulcer
Accelerated healing of chronic sickle-cell leg ulcers treated with RGD peptide matrix. RGD Study Group.
Autologous stem cell-based therapy for sickle cell leg ulcer: a pilot study.
Common, But Neglected: A Comprehensive Review of Leg Ulcers in Sickle Cell Disease.
Cutaneous adverse reactions to hydroxyurea in patients with sickle cell disease.
Degree of Anemia, Indirect Markers of Hemolysis, and Vascular Complications of Sickle Cell Disease in Africa.
Depression and loneliness in Jamaicans with sickle cell disease.
Genome-wide association study of erythrocyte density in sickle cell disease patients.
Hydroxyurea for the treatment of sickle cell disease.
Inflammation in sickle cell disease.
Insights into the skin microbiome of sickle cell disease leg ulcers.
Intima-media thickness of the common femoral artery as a marker of leg ulceration in sickle cell disease patients.
Leg ulcer induced by hydroxycarbamide in sickle cell disease: What is the therapeutic impact?
Leg ulcers in sickle cell disease.
Low nitric oxide level is implicated in sickle cell disease and its complications in Ghana.
Microfluidics in Sickle Cell Disease Research: State of the Art and a Perspective Beyond the Flow Problem.
Mini review: leg ulcers - a secondary complication of sickle cell disease.
Multimodality Treatment for Nonhealing Wound With Osteomyelitis in Sickle Cell Disease.
Pain syndromes in sickle cell disease: an update.
Polymorphisms in Inflammatory Genes Modulate Clinical Complications in Patients With Sickle Cell Disease.
Prevalence and Predictive Factors for Leg Ulcers in Sickle Cell Disease Patients in Saudi Arabia: A Cross-Sectional Observational Study.
Sickle Cell Anemia and Comorbid Leg Ulcer Treated With Curative Peripheral Blood Stem Cell Transplantation.
Sickle cell disease as a vascular disorder.
Sickle cell disease induces resistance to cutaneous carcinogenesis.
Sickle cell disease subphenotypes in patients from southwestern province of saudi arabia.
Sickle cell leg ulcers: a frequently disabling complication and a marker of severity.
Steady-state sVCAM-1 serum levels in adults with sickle cell disease.
Subclinical Cardiac Dysfunction Is Associated With Extracardiac Organ Damages.
Successful Management of a Chronic Refractory Leg Ulcer in an Adolescent with Sickle Cell Anemia.
Successful pulmonary thromboendarterectomy in a patient with sickle cell disease and associated resolution of a leg ulcer.
The anaerobic and aerobic bacterial flora of leg ulcers in patients with sickle-cell disease.
The psychosocial impact of leg ulcers in patients with sickle cell disease: I don't want them to know my little secret.
The Red Blood Cell-Inflammation Vicious Circle in Sickle Cell Disease.
The role of the arginine metabolome in pain: implications for sickle cell disease.
Topical effectiveness of molgramostim (GM-CSF) in sickle cell leg ulcers.
Treatment of recalcitrant chronic leg ulcer in a known sickle cell anaemia patient using honey and fresh hbaa red cell concentrate in a Nigerian secondary healthcare facility.
Vasculopathy, inflammation, and blood flow in leg ulcers of patients with sickle cell anemia.
[Potential alternatives to erythrocyte transfusion in hemoglobinopathies: hydroxyurea (HU), erythropoietin (EPO), butyrate derivatives, blood substitutes]
Leiomyoma
The Prevalence of Uterine Fibroids in African American Women with Hemoglobin SS Sickle Cell Disease as Determined by Pelvic Magnetic Resonance Imaging.
Leukemia
Acquired DNA mutations associated with in vivo hydroxyurea exposure.
Bone marrow necrosis in sickle cell disease: a description of three cases and a review of the literature.
Metabolic adaptation of acute lymphoblastic leukemia to the central nervous system microenvironment is dependent on Stearoyl CoA desaturase.
Sickle cell anemia and hematological neoplasias.
[Cytogenetic studies on 334 myelodysplastic syndrome (MDS), aplastic anemia (AA) and other hematological diseases]
[Relationship between the occurrences of AL, MDS and AA and abnormal BM proliferation of patient's parents]
Leukemia, Erythroblastic, Acute
Dimethyl fumarate increases fetal hemoglobin, provides heme detoxification, and corrects anemia in sickle cell disease.
Intense leuco-erythroblastic blood picture resembling erythro-leukaemia in sickle cell disease: a case report.
Leukemia, Hairy Cell
Sickle cell anemia and hematological neoplasias.
Leukemia, Lymphocytic, Chronic, B-Cell
Clinical significance of sIL2R, sCD23, sICAM-1, IL6 and sCD 14 serum levels in B-cell chronic lymphocytic leukemia.
Leukemia, Myeloid, Acute
Transfusional iron burden and liver toxicity after bone marrow transplantation for acute myelogenous leukemia and hemoglobinopathies.
Leukemia, T-Cell
Analysis of Risk Factors Associated With Poor Outcome in Posterior Reversible Encephalopathy Syndrome After Treatment in Children: Systematic Review and Meta-Analysis.
Leukocytosis
Effects of experimental asthma on inflammation and lung mechanics in sickle cell mice.
Leukocyte numbers correlate with plasma levels of granulocyte-macrophage colony-stimulating factor in sickle cell disease.
Leukocytosis is a risk factor for lung function deterioration in children with sickle cell disease.
Placenta growth factor activates monocytes and correlates with sickle cell disease severity.
The Role of Inflammation and Leukocytes in the Pathogenesis of Sickle Cell Disease.
The Role of Inflammation and Leukocytes in the Pathogenesis of Sickle Cell Disease; Haemoglobinopathy.
Lipid Metabolism Disorders
Critical role of miR-125b in lipogenesis by targeting stearoyl-CoA desaturase-1 (SCD-1).
Lipodystrophy
The Role of Promyelocytic Leukemia Protein in Steatosis-Associated Hepatic Tumors Related to Chronic Hepatitis B virus Infection.
Lipoma
Benign cardiac tumours associated with sudden death.
Lipomatosis
[Significance of nonspecific histopathologic changes in the myocardium in sudden coronary death]
Livedoid Vasculopathy
Livedoid Vasculopathy Presenting in a Patient With Sickle Cell Disease.
Liver Abscess
An Hepatic Abscess in a Patient with Sickle Cell Anemia.
Pyogenic hepatic abscess after percutaneous liver biopsy in a patient with sickle cell disease.
Liver Cirrhosis
Emerging therapies for the treatment of nonalcoholic steatohepatitis: A systematic review.
Liver Stiffness Measurement With FibroScan: Use the Right Probe in the Right Conditions!
Stearoyl-CoA Desaturase Promotes Liver Fibrosis and Tumor Development in Mice via a Wnt Positive-Signaling Loop by Stabilization of Low-Density Lipoprotein-Receptor-Related Proteins 5 and 6.
[Expression of c-erbB-2 protein and EGF receptor in hepatitis B, cirrhosis and hepatocellular carcinoma]
Liver Cirrhosis, Alcoholic
Autonomic dysfunction in alcoholic cirrhosis and its relation to sudden cardiac death risk predictors.
Liver Diseases
Acute and chronic hepatobiliary manifestations of sickle cell disease: A review.
Association of pro-inflammatory high-density lipoprotein cholesterol with clinical and laboratory variables in sickle cell disease.
Autoimmune Liver Disease in Patients With Sickle Cell Disease.
Correlation of serum cholylglycine level with hepatic dysfunction in children with sickle cell anemia.
Dietary polyunsaturated fatty acids mediate the inverse association of stearoyl-CoA desaturase activity with the risk of fatty liver in dyslipidaemic individuals.
Emerging therapies for the treatment of nonalcoholic steatohepatitis: A systematic review.
Fatty Acid Desaturase Involvement in Non-Alcoholic Fatty Liver Disease Rat Models: Oxidative Stress Versus Metalloproteinases.
Fatty Liver Is Associated with Transcriptional Downregulation of Stearoyl-CoA Desaturase and Impaired Protein Dimerization.
Gastrointestinal and Hepatic Complications of Sickle Cell Disease.
Geniposide and Chlorogenic Acid Combination Improves Non-Alcoholic Fatty Liver Disease Involving the Potent Suppression of Elevated Hepatic SCD-1.
Hepatic lipid partitioning and liver damage in nonalcoholic fatty liver disease: role of stearoyl-CoA desaturase.
How we treat sickle hepatopathy and liver transplantation in adults.
In a pilot study, reduced fatty acid desaturase 1 function was associated with nonalcoholic fatty liver disease and response to treatment in children.
Isolation and Anti-Fatty Liver Activity of a Novel Cerebroside from the Sea Cucumber Acaudina molpadioides.
Liver injury is associated with mortality in sickle cell disease.
Liver Stiffness Measurement by Vibration Controlled Transient Elastography Does Not Correlate to Hepatic Iron Overload in Children With Sickle Cell Disease.
Liver Transplantation in Patients with Sickle Cell Disease in the United States.
Liver transplantation in patients with sickle cell disease: possible but challenging-a cohort study.
miR-192-5p regulates lipid synthesis in non-alcoholic fatty liver disease through SCD-1.
n-3 Polyunsaturated fatty acids for the management of alcoholic liver disease: A critical review.
Recent advances on stearoyl-CoA desaturase regulation in fatty liver diseases.
Stearoyl-CoA desaturase and tumorigenesis.
Stearoyl-CoA desaturase, a short-lived protein of endoplasmic reticulum with multiple control mechanisms.
TXNIP/VDUP1 attenuates steatohepatitis via autophagy and fatty acid oxidation.
Vitamin A deficiency increases the oleic acid (C18:1) levels in the kidney of high fructose diet-fed rats.
[Research progress of stearoyl-CoA desaturase-1 on obesity and non-alcoholic fatty liver disease Abstract].
Liver Diseases, Alcoholic
n-3 Polyunsaturated fatty acids for the management of alcoholic liver disease: A critical review.
Liver Failure
Gastrointestinal pathology in sickle cell disease.
Toward dual hematopoietic stem-cell transplantation and solid-organ transplantation for sickle-cell disease.
Liver Failure, Acute
Liver transplantation in patients with sickle cell disease: possible but challenging-a cohort study.
Liver Neoplasms
Sorafenib kills liver cancer cells by disrupting SCD1-mediated synthesis of monounsaturated fatty acids via the ATP-AMPK-mTOR-SREBP1 signaling pathway.
Sphere-forming culture enriches liver cancer stem cells and reveals Stearoyl-CoA desaturase 1 as a potential therapeutic target.
Liver Neoplasms, Experimental
Analysis of the stearoyl-CoA desaturase system in the Morris hepatoma 7288C and 7288CTC.
Stearoyl-coenzyme A desaturase activity in Novikoff hepatoma.
The importance of the stearoyl-CoA desaturase system in octadecenoate metabolism in the Morris hepatoma 7288C.
Long QT Syndrome
Can sudden cardiac death in the young be predicted and prevented? Lessons from autopsy for the emergency physician.
Cardiac Screening for High Risk Sudden Cardiac Death in School-Aged Children.
Cardiovascular genomics.
Electrocardiogram Screening for Disorders That Cause Sudden Cardiac Death in Asymptomatic Children: A Meta-analysis.
Electrocardiograms in athletes: interpretation and diagnostic accuracy.
Electrocardiographic Screening for Hypertrophic Cardiomyopathy and Long QT Syndrome: The Drivers of Cost-Effectiveness for the Prevention of Sudden Cardiac Death.
Exercise and Inherited Arrhythmias.
Genetics of sudden cardiac death syndromes.
Inherited Arrhythmia Syndrome Predisposing to Sudden Cardiac Death.
Monogenec Arrhythmic Syndromes: From Molecular and Genetic Aspects to Bedside.
Prevalence of arrhythmia-associated gene mutations and risk of sudden cardiac death in the Finnish population.
Prolonged QTc interval predicts all-cause mortality in patients with rheumatoid arthritis: an association driven by high inflammatory burden.
Recent developments in the management of patients at risk for sudden cardiac death.
Risk factors for sudden cardiac death to determine high risk patients in specific patient populations that may benefit from a wearable defibrillator.
Sudden cardiac death in children and adolescents (excluding Sudden Infant Death Syndrome).
Sudden cardiac death in infants, children, and adolescents.
Sudden cardiac death in Long QT syndrome (LQTS), Brugada syndrome, and catecholaminergic polymorphic ventricular tachycardia (CPVT).
Sudden cardiac death in young athletes; a literature review and special considerations in Asia.
Sudden cardiac death in young competitive athletes due to genetic cardiac abnormalities.
Sudden cardiac death.
The association between SCN5A, KCNQ1 and KCNE1 gene polymorphisms and complex ventricular arrhythmias in survivors of myocardial infarction.
The Postmortem Interpretation of Cardiac Genetic Variants of Unknown Significance in Sudden Death in the Young: A Case Report and Review of the Literature.
Lung Diseases
Asthma in children with sickle cell disease.
Asthma in sickle cell disease.
Asthma, allergic sensitization and lung function in sickle cell disease.
Circulating fibrocytes as biomarkers of impaired lung function in adults with sickle cell disease.
Curing Hemoglobinopathies: Challenges and Advances of Conventional and New Gene Therapy Approaches.
Decreased exhaled nitric oxide in sickle cell disease: relationship with chronic lung involvement.
Diffuse cystic lung disease in sickle cell anaemia: a series of 22 cases and a case-control study.
Functional capacity in children and young adults with sickle cell disease undergoing evaluation for cardiopulmonary disease.
Identifying Clinical and Research Priorities in Sickle Cell Lung Disease. An Official American Thoracic Society Workshop Report.
Leukocytosis is a risk factor for lung function deterioration in children with sickle cell disease.
Pulmonary complications of sickle cell disease: a narrative clinical review.
Pulmonary disease burden in Hispanic and non-Hispanic children with sickle cell disease.
Pulmonary hypertension in children and adolescents with sickle cell disease.
Pulmonary hypertension in sickle cell disease.
Technetium 99m-diethylene triamine penta-acetic acid aerosol clearance in the evaluation of pulmonary involvement in sickle cell disease.
Lung Diseases, Obstructive
Airway Inflammation and Lung Function in Sickle Cell Disease.
Airway inflammation in sickle cell disease-A translational perspective.
Asthma and sickle cell disease: two distinct diseases or part of the same process?
NT-proBNP levels and cardiopulmonary function in children with sickle cell disease.
Prediction of sudden death in elderly patients with heart failure.
Lung Injury
Adenosine A2A receptors induced on iNKT and NK cells reduce pulmonary inflammation and injury in mice with sickle cell disease.
Ambulatory hypertension in a pediatric cohort of sickle cell disease.
Chlorine inhalation induces acute chest syndrome in humanized sickle cell mouse model and ameliorated by postexposure hemopexin.
Endothelial TLR4 Expression Mediates Vaso-Occlusive Crisis in Sickle Cell Disease.
Extracellular hemin crisis triggers acute chest syndrome in sickle mice.
Hypoxia-induced acute lung injury in murine models of sickle cell disease.
Nonhematopoietic Nrf2 dominantly impedes adult progression of sickle cell anemia in mice.
Quantitative intravital two-photon excitation microscopy reveals absence of pulmonary vaso-occlusion in unchallenged Sickle Cell Disease mice.
Streptococcus pneumoniae and Its Virulence Factors H2O2 and Pneumolysin Are Potent Mediators of the Acute Chest Syndrome in Sickle Cell Disease.
Lung Neoplasms
A novel autoantibody test for the detection of Pre-neoplastic lung lesions.
Inhibition of stearoylCoA desaturase activity blocks cell cycle progression and induces programmed cell death in lung cancer cells.
Stearoyl-CoA desaturase activity modulates the activation of epidermal growth factor receptor in human lung cancer cells.
[Report of a case of small cell lung cancer associated with Lambert-Eaton myasthenic syndrome and subacute cerebellar degeneration--with a review of the Japanese literature]
Lupus Erythematosus, Systemic
Systemic lupus erythematosus in patients with sickle cell disease.
Lupus Nephritis
Lupus nephritis in a patient with sickle cell disease.
Lupus Vulgaris
Incidence of cutaneous tuberculosis in patients with organ tuberculosis.
Lymphadenitis
Incidence of cutaneous tuberculosis in patients with organ tuberculosis.
Lymphadenopathy
Mantle Cell Hyperplasia of Peripheral Lymph Nodes as Initial Manifestation of Sickle Cell Disease.
Lymphatic Metastasis
HER2/neu negative salivary duct carcinoma of parotid: A case with forty months recurrence free follow up.
Prognostic factor identification by screening changes in differentially expressed genes in oral squamous cell carcinoma.
Squamous Cell Differentiation in Metastatic Papillary Thyroid Carcinoma: Metaplastic Reversion or Progression?
The role of stearoyl-coenzyme A desaturase 1 in clear cell renal cell carcinoma.
Lymphedema
Risk of secondary lymphedema in breast cancer survivors is related to serum phospholipid fatty acid desaturation.
The Health Deviation of Post-Breast Cancer Lymphedema: Symptom Assessment and Impact on Self-Care Agency.
Lymphoma
C. elegans anaplastic lymphoma kinase ortholog SCD-2 controls dauer formation by modulating TGF-beta signaling.
Subcutaneous panniculitis-like T-cell lymphoma in a 25-year-old male patient with sickle cell disease.
The MLK-1/SCD-4 Mixed Lineage Kinase/MAP3K functions to promote dauer formation upstream of DAF-2/InsR.
Tumor burden and serum level of soluble CD25, CD8, CD23, CD54 and CD44 in non-Hodgkin's lymphoma.
Lymphoma, T-Cell
Subcutaneous panniculitis-like T-cell lymphoma in a 25-year-old male patient with sickle cell disease.
Lymphopenia
Spinal cord dysfunction after COVID-19 infection.
Splenic morphological changes are accompanied by altered baseline immunity in a mouse model of sickle-cell disease.
Machado-Joseph Disease
Compound heterozygous intermediate MJD alleles cause cerebellar ataxia with sensory neuropathy.
Difference in the Effects of Tandospirone on Ataxia in Various Types of Spinocerebellar Degeneration: An Open-Label Study.
Vestibular evoked myogenic potentials in patients with spinocerebellar degeneration.
[A case of spinocerebellar ataxia type 3 (SCA3) associated with isolated ACTH deficiency]
[A refined evaluation of cerebellar ataxia and its application to treatment of spinocerebellar degeneration]
[An MRI study of hereditary spinocerebellar degenerations]
[Autosomal dominant spinocerebellar degeneration--new forms and pathomechanisms]
[Overview of Hereditary Spinocerebellar Ataxias in Japan].
[Spinocerebellar degeneration in Japan--the feature from an epidemiological study]
[Study on argyrophilic inclusions of multisystem atrophy (Oppenheimer)]
Macular Degeneration
Efficient Quantitative Analysis of Carboxyalkylpyrrole Ethanolamine Phospholipids: Elevated Levels in Sickle Cell Disease Blood.
Genome-Wide Transcriptomic Analysis Identifies Pathways Regulated by Sterculic Acid in Retinal Pigmented Epithelium Cells.
Multifocal electroretinogram findings in sickle cell maculopathy.
Sickle cell maculopathy: Identification of systemic risk factors, and microstructural analysis of individual retinal layers of the macula.
Sickle cell retinopathy: What we now understand using optical coherence tomography angiography. A systematic review.
Sterculic Acid: The Mechanisms of Action beyond Stearoyl-CoA Desaturase Inhibition and Therapeutic Opportunities in Human Diseases.
Malaria
A randomized trial of artesunate-amodiaquine versus artemether-lumefantrine in Ghanaian paediatric sickle cell and non-sickle cell disease patients with acute uncomplicated malaria.
A randomized trial to compare the safety, tolerability and effectiveness of three antimalarial regimens for the prevention of malaria in Nigerian patients with sickle-cell disease.
Analysis of clinical presentation, hematological factors, self-reported bed net usage, and malaria burden in sickle cell disease patients.
Association between haematological parameters and sickle cell genotypes in children with Plasmodium falciparum malaria resident in Kisumu County in Western Kenya.
Asymptomatic malaria parasitaemia in sickle-cell disease patients: how effective is chemoprophylaxis?
Effect of active prenatal management on pregnancy outcome in sickle cell disease in an African setting.
Evaluation of hematological indices of childhood illnesses in Tamale Metropolis of Ghana.
Hemoglobin Genotypes Modulate Inflammatory Response to Plasmodium Infection.
Hereditary elliptocytosis-associated alpha-spectrin mutation p.L155dup as a modifier of sickle cell disease severity.
High prevalence of Plasmodium falciparum pfcrt K76T mutation in children with sickle cell disease at a tertiary hospital in north-western Tanzania.
Improvement of SCD morbimortality in children: experience in a remote area of an African country.
Malaria as a cause of morbidity and mortality in children with homozygous sickle cell disease on the coast of Kenya.
Malaria in patients with sickle cell anaemia: burden, risk factors and outcome at the Laquintinie hospital, Cameroon.
Microvasculature-on-a-chip for the long-term study of endothelial barrier dysfunction and microvascular obstruction in disease.
Monthly sulphadoxine-pyrimethamine combination versus daily proguanil for malaria chemoprophylaxis in sickle cell disease: a randomized controlled study at the Jos University Teaching Hospital.
Negative Epistasis between Sickle and Foetal Haemoglobin Suggests a Reduction in Protection against Malaria.
Pathology of sickle cell disease.
Plasma Folate Levels in Acutely Ill and Steady State Pediatric Sickle Cell Disease Patients in Ghana.
Population Pharmacokinetic Estimates Suggest Elevated Clearance and Distribution Volume of Desethylamodiaquine in Pediatric Patients with Sickle Cell Disease Treated with Artesunate-Amodiaquine.
Prevalence and factors associated with renal dysfunction in children admitted to two hospitals in northwestern Tanzania.
Prevalence of Plasmodium falciparum and non-P. falciparum infections in a highland district in Ghana, and the influence of HIV and sickle cell disease.
Safety and effectiveness of antimalarial therapy in sickle cell disease: a systematic review and network meta-analysis.
Severe oxidative stress in sickle cell disease patients with uncomplicated Plasmodium falciparum malaria in Kampala, Uganda.
Sickle cell disease and malaria morbidity: a tale with two tails.
Sickle cell disease and malaria: decreased exposure and asplenia can modulate the risk from Plasmodium falciparum.
Sickle cell disease in Africa: a neglected cause of early childhood mortality.
Sickle cell disease in southwestern Nigeria: assessment of knowledge of primary health care workers and available facilities.
Sickle cell disease: a neglected chronic disease of increasing global health importance.
Sickle cell disease: current activities, public health implications, and future directions.
Sickle-cell disease and malaria: evaluation of seasonal intermittent preventive treatment with sulfadoxine-pyrimethamine in Senegalese patients-a randomized placebo-controlled trial.
Sickle-cell disease in febrile children living in a rural village of Madagascar and association with malaria and respiratory infections.
Suspected Severe Malaria in a Sudanese Patient Affected by Sickle Cell Disease Who Was Treated with Hydroxyurea.
Systematic review of current and emerging strategies for reducing morbidity from malaria in sickle cell disease.
The CYB5R3c.350C>G and G6PD A alleles modify severity of anemia in malaria and sickle cell disease.
The incidence of malaria and the comparison of hematological and biochemical indices of Plasmodium falciparum-parasitemic and aparasitemic sickle cell disease (SCD) patients.
Transfusion-transmitted malaria masquerading as sickle cell crisis with multisystem organ failure.
Turf wars: exploring splenomegaly in sickle cell disease in malaria-endemic regions.
Utilization patterns of malaria chemoprophylaxis among Tanzanian children attending sickle cell clinic in Dar es Salaam tertiary hospitals.
Malnutrition
Degree of Anemia, Indirect Markers of Hemolysis, and Vascular Complications of Sickle Cell Disease in Africa.
Dietary intakes and nutritional status of children with sickle cell disease at the Princess Marie Louise Hospital, Accra - a survey.
Epidemiology and treatment of relative anemia in children with sickle cell disease in sub-Saharan Africa.
Expression of SCD and FADS2 Is Lower in the Necrotic Core and Growing Tumor Area than in the Peritumoral Area of Glioblastoma Multiforme.
Head circumference of children with sickle cell disease in Lagos, Nigeria.
Impaired pubertal development and testicular hormone function in males with sickle cell anemia.
In Vitro Lymphocyte Functions in Undernourished Children With Sickle Cell Anemia.
Influence of Nutrition on Disease Severity and Health-related Quality of Life in Adults with Sickle Cell Disease: A Prospective Study.
Life-Threatening Infectious Complications in Sickle Cell Disease: A Concise Narrative Review.
Multiple complications in sickle cell anaemia.
Nutritional perspectives on sickle cell disease in Africa: a systematic review.
Nutritional status of children with sickle cell disease at korle bu teaching hospital, accra, ghana.
Prevalence and factors associated with renal dysfunction among children with sickle cell disease attending the sickle cell disease clinic at a tertiary hospital in Northwestern Tanzania.
Pulmonary function correlates with body composition in Nigerian children and young adults with sickle cell disease.
Sickle cell disease in Africa: a neglected cause of early childhood mortality.
Total and resting energy expenditure in children with sickle cell disease.
Variations in sexual dimorphism in the skulls of rats subjected to malnutrition, castration, and treatment with gonadal hormones.
Malocclusion
Anthropometric finding in Nigerian children with sickle cell disease.
Malocclusion and treatment need in children and adolescents with sickle cell disease.
Occlusal Disorders in Patients with Sickle Cell Disease: Critical Literature Review.
Marfan Syndrome
Cardiac Screening for High Risk Sudden Cardiac Death in School-Aged Children.
Electrocardiograms in athletes: interpretation and diagnostic accuracy.
Heart rate turbulence and deceleration capacity for risk prediction of serious arrhythmic events in Marfan syndrome.
Sudden cardiac death in young athletes; a literature review and special considerations in Asia.
Masked Hypertension
Abnormal Ambulatory Blood Pressure and Early Renal Dysfunction in Sickle Cell Disease.
Ambulatory hypertension in a pediatric cohort of sickle cell disease.
Mastitis
Stearoyl-CoA desaturase 1 expression is downregulated in liver and udder during E. coli mastitis through enhanced expression of repressive C/EBP factors and reduced expression of the inducer SREBP1A.
Maternal Death
Morbidity and pregnancy outcomes associated with sickle cell anemia among Saudi women.
Pregnancy in patients with sickle cell disease: maternal and perinatal outcomes.
Pregnancy outcome in patients with homozygous sickle cell disease in a university hospital, Eastern Saudi Arabia.
Sickle cell disease and pregnancy in Bahrain.
Sickle cell disease in pregnancy: trend and pregnancy outcomes at a tertiary hospital in Tanzania.
Sickle cell disease related mortality in Brazil, 2000-2018.
Measles
Immunologic effects of hydroxyurea in sickle cell anemia.
Meibomian Gland Dysfunction
Compensatory increases in tear volume and mucin levels associated with meibomian gland dysfunction caused by stearoyl-CoA desaturase-1 deficiency.
Melanoma
An omega-3 polyunsaturated fatty acid derivative, 18-HEPE, protects against CXCR4-associated melanoma metastasis.
Endogenously synthesized n-3 fatty acids in fat-1 transgenic mice prevent melanoma progression by increasing E-cadherin expression and inhibiting ?-catenin signaling.
Gene expression changes associated with chemically induced rat mammary carcinogenesis.
Inhibition of Stearoyl-CoA desaturase 1 reverts BRAF and MEK inhibition-induced selection of cancer stem cells in BRAF-mutated melanoma.
Lineage-Restricted Regulation of SCD and Fatty Acid Saturation by MITF Controls Melanoma Phenotypic Plasticity.
Melanoma tumor growth is accelerated in a mouse model of sickle cell disease.
SCD5-induced oleic acid production reduces melanoma malignancy by intracellular retention of SPARC and cathepsin B.
The Occurrence and Proposed Significance of Schnabel Cavernous Degeneration in Uveal Melanoma.
Melanosis
Primary pigmented meningeal melanocytoma originating in Meckel cave in a patient with carney complex: A case report.
Memory Disorders
A High-Fructose-High-Coconut Oil Diet Induces Dysregulating Expressions of Hippocampal Leptin and Stearoyl-CoA Desaturase, and Spatial Memory Deficits in Rats.
Amyloid Plaques and Symptoms of Depression Links to Medical Help-Seeking due to Subjective Cognitive Decline.
Amyloid-? Load Is Related to Worries, but Not to Severity of Cognitive Complaints in Individuals With Subjective Cognitive Decline: The SCIENCe Project.
Cross-sectional association between physical activity level and subjective cognitive decline among US adults aged ?45 years, 2015.
Gendered racial differences and similarities in subjective cognitive decline and life satisfaction: results from a population-based sample.
Racial and ethnic differences in post-stroke subjective cognitive decline exist.
Unmet needs for assistance related to subjective cognitive decline among community-dwelling middle-aged and older adults in the US: prevalence and impact on health-related quality of life.
Working Memory in Children With Neurocognitive Effects From Sickle Cell Disease: Contributions of the Central Executive and Processing Speed.
Meniere Disease
Dehiscence of the posterior semicircular canal.
Meningitis
Penicillin- and cephalosporin-resistant strains of Streptococcus pneumoniae causing sepsis and meningitis in children with sickle cell disease.
Seizures risk factors in sickle cell disease. The cooperative study of sickle cell disease.
[Infectious complications after surgical splenectomy in children with sickle cell anemia disease].
Meningitis, Pneumococcal
Infections and sickle cell disease in Eastern Saudi Arabian children.
Meningocele
Spondylocostal dysostosis associated with right-sided polythelia, right-sided rib deformity and meningocoele: Case report with review of literature.
Menopause, Premature
Fertility challenges for women with sickle cell disease.
Menorrhagia
Bleeding in patients with sickle cell disease: a population-based study.
Common gynecological challenges in adolescents with sickle cell disease.
MERRF Syndrome
[Study on argyrophilic inclusions of multisystem atrophy (Oppenheimer)]
Metabolic Diseases
Association between increased visceral fat area and alterations in plasma fatty acid profile in overweight subjects: a cross-sectional study.
Biochemical and Physiological Function of Stearoyl-CoA Desaturase.
Crystal structure of human stearoyl-coenzyme A desaturase in complex with substrate.
Discovery of tumor-specific irreversible inhibitors of stearoyl CoA desaturase.
Global expression and CpG methylation analysis of primary endothelial cells before and after TNFa stimulation reveals gene modules enriched in inflammatory and infectious diseases and associated DMRs.
Insights into Stearoyl-CoA Desaturase-1 Regulation of Systemic Metabolism.
Novel substituted heteroaromatic compounds as inhibitors of stearoyl-CoA desaturase.
Plasma-based approach to measure target engagement for liver-targeting stearoyl-CoA desaturase 1 inhibitors.
Stearoyl-CoA desaturase and tumorigenesis.
Stearoyl-CoA desaturase inhibitors: update on patented compounds.
Stearoyl-CoA desaturase-1 and adaptive stress signaling.
The role of stearoyl-CoA desaturase in body weight regulation.
Metabolic Syndrome
Absence of stearoyl-CoA desaturase-1 ameliorates features of the metabolic syndrome in LDLR-deficient mice.
Accumulation of lipids and oxidatively damaged DNA in hepatocytes exposed to particles.
Combined Therapy of Dietary Fish Oil and Stearoyl-CoA Desaturase 1 Inhibition Prevents the Metabolic Syndrome and Atherosclerosis.
Differences in arachidonic acid levels and fatty acid desaturase ( FADS) gene variants in African Americans and European Americans with diabetes or the metabolic syndrome.
Discovery of piperazin-1-ylpyridazine-based potent and selective stearoyl-CoA desaturase-1 inhibitors for the treatment of obesity and metabolic syndrome.
Docosahexaenoic Acid Content in Plasma Phospholipids and Desaturase Indices in Obese Children.
Effects of diet and genetic background on sterol regulatory element-binding protein-1c, stearoyl-CoA desaturase 1, and the development of the metabolic syndrome.
Fatty acid composition of serum lipids predicts the development of the metabolic syndrome in men.
Genetic variation in stearoyl-CoA desaturase 1 is associated with metabolic syndrome prevalence in Costa Rican adults.
Inhibition of stearoyl-coenzyme A desaturase 1 dissociates insulin resistance and obesity from atherosclerosis.
Leptin and the control of metabolism: role for stearoyl-CoA desaturase-1 (SCD-1).
Metabolic syndrome and the risk of sudden cardiac death in middle-aged men.
Microbiota-Dependent Hepatic Lipogenesis Mediated by Stearoyl CoA Desaturase 1 (SCD1) Promotes Metabolic Syndrome in TLR5-Deficient Mice.
Modulation of tissue fatty acids by L-carnitine attenuates metabolic syndrome in diet-induced obese rats.
Protein engineering: Regulatory perspectives of stearoyl CoA desaturase.
Role of hepatic desaturases in obesity-related metabolic disorders.
SCD in the world, Europe, Bosnia and Herzegovina and Mostar.
Stearoyl-CoA desaturase as a new drug target for obesity treatment.
Stearoyl-CoA Desaturase Promotes Liver Fibrosis and Tumor Development in Mice via a Wnt Positive-Signaling Loop by Stabilization of Low-Density Lipoprotein-Receptor-Related Proteins 5 and 6.
Stearoyl-CoA desaturase-1 and the metabolic syndrome.
Stearoyl-CoA Desaturase: A Vital Checkpoint in the Development and Progression of Obesity.
Stearoyl-coenzyme A desaturase 1 inhibition and the metabolic syndrome: considerations for future drug discovery.
Microaneurysm
Microvascular abnormalities in sickle cell disease: a computer-assisted intravital microscopy study.
Migraine Disorders
A dipole model for spreading cortical depression.
Analysis of MEG signals of spreading cortical depression with propagation constrained to a rectangular cortical strip. II. Gyrencephalic swine model.
Health status and healthcare use in a national sample of children with sickle cell disease.
Modeling the spreading cortical depression wavefront.
Neurologic complications in children under five years with sickle cell disease.
Presence of pain on three or more days of the week is associated with worse patient reported outcomes in adults with sickle cell disease.
Simulating the propagation of spreading cortical depression (SCD) wavefront on human brain surface.
Subjective cognitive decline in patients with migraine and its relationship with depression, anxiety, and sleep quality.
Mitochondrial Diseases
Sudden cardiac death in neuromuscular disorders.
Mitral Valve Insufficiency
The Risk of Sudden Cardiac Death in Mitral Valve Prolapse: Are All Patients Created Equal?
[A case of mitral valve prolapse with increased risk for sudden cardiac death in an athlete].
Mitral Valve Prolapse
A case of sudden cardiac death following Domperidone self-medication.
Association Between Malignant Mitral Valve Prolapse and Sudden Cardiac Death: A Review.
Detecting Underlying Cardiovascular Disease in Young Competitive Athletes.
Electrocardiograms in athletes: interpretation and diagnostic accuracy.
Mitral Prolapse: An Old Mysterious Entity - The Incremental Role of Multimodality Imaging in Sports Eligibility.
Mitral Valve Prolapse and Sudden Cardiac Death: A Systematic Review.
Role of echocardiography in screening and evaluation of athletes.
[Sudden cardiac death in women].
Motor Neuron Disease
Electron spin resonance studies of erythrocyte membrane in spinocerebellar degeneration.
Glutamate dehydrogenase deficiency in spinocerebellar degenerations.
Mouth Neoplasms
FADS1 rs174549 Polymorphism May Predict a Favorable Response to Chemoradiotherapy in Oral Cancer Patients.
Novel polymorphism in FADS1 gene and fish consumption on risk of oral cancer: A case-control study in southeast China.
Movement Disorders
Nitrous Oxide-induced Subacute Combined Degeneration Presenting with Dystonia and Pseudoathetosis: A Case Report.
Moyamoya Disease
Characteristics of Moyamoya Syndrome in Sickle-Cell Disease by Magnetic Resonance Angiography: An Adult-Cohort Study.
Childhood stroke in Eastern Province, KSA: pattern, risk factors, diagnosis and outcome.
Diagnostic approach and management strategy of childhood stroke.
Effectiveness of surgical revascularization for stroke prevention in pediatric patients with sickle cell disease and moyamoya syndrome.
Hematologic risk factors for stroke in Saudi children.
Intracranial Aneurysms in Sickle-Cell Disease Are Associated With the Hemoglobin SS Genotype But Not With Moyamoya Syndrome.
Thrombolytic therapy for the treatment of acute ischaemic stroke in adults with homozygous sickle cell disease.
Treatment of a cerebral pial arteriovenous fistula in a patient with sickle cell disease-related moyamoya syndrome: case report.
Multiple Endocrine Neoplasia Type 2a
Effects of hydroxyurea treatment on cerebral oxygenation in adult patients with sickle cell disease: an open-label pilot study.
Multiple Endocrine Neoplasia Type 2b
Sudden cardiac death after manual or automated snow removal.
Multiple Myeloma
Differential diagnosis of Schnyder corneal dystrophy.
Sickle cell anemia and hematological neoplasias.
Multiple Sclerosis
Oral Monomethyl Fumarate Therapy Ameliorates Retinopathy in a Humanized Mouse Model of Sickle Cell Disease.
Staphylococcus aureus colonization in community-dwelling people with spinal cord dysfunction.
Unmet needs of multiple sclerosis patients in the community.
Multiple System Atrophy
Cognitive impairment in spinocerebellar degeneration.
Distinguishing spinocerebellar ataxia with pure cerebellar manifestation from multiple system atrophy (MSA-C) through saccade profiles.
Prevalence of spinocerebellar degenerations in the Hokuriku district in Japan.
Short-Term Effect of Intensive Speech Therapy on Dysarthria in Patients With Sporadic Spinocerebellar Degeneration.
[Cerebrospinal fluid levels of 28 kDa calcium-binding protein in patients with neurological diseases]
[The Nomenclature and Classification of Sporadic Spinocerebellar Degeneration].
Mumps
Immunologic effects of hydroxyurea in sickle cell anemia.
Muscle Cramp
Vaso-Occlusive Pain and Menstruation in Sickle Cell Disease: A Focus Group Analysis.
Muscle Weakness
Juvenile polymyositis with unremitting pain and progressive loss of motor and bulbar function on a background of sickle cell disease.
Muscular Atrophy
Reduction of stearoyl-CoA desaturase (SCD) contributes muscle atrophy through the excess endoplasmic reticulum stress in chronic kidney disease.
Muscular Diseases
Carnitine transport by organic cation transporters and systemic carnitine deficiency.
Musculoskeletal Pain
Iliopsoas hematoma in a patient with sickle cell disease.
Myalgia
Juvenile polymyositis with unremitting pain and progressive loss of motor and bulbar function on a background of sickle cell disease.
Mycoses
The inhibitory effect of cerulenin to yeasts is fungicidal.
Myocardial Bridging
Electrocardiograms in athletes: interpretation and diagnostic accuracy.
Update on the Diagnostic Pitfalls of Autopsy and Post-Mortem Genetic Testing in Cardiomyopathies.
Myocardial Infarction
A common variant at 9p21 is associated with sudden and arrhythmic cardiac death.
Activity immediately before the onset of non-fatal myocardial infarction and sudden cardiac death.
Amino-terminal pro-brain natriuretic peptide predicts ventricular arrhythmogenesis in patients with ischemic cardiomyopathy and implantable cardioverter-defibrillators.
Antihypertensive therapy and sudden cardiac death, should we expect the unexpected?
Arrhythmogenic right ventricular cardiomyopathy and sudden cardiac death in young Koreans.
Association between Clinical and Doppler Echocardiographic Parameters with Sudden Death in Hemodialysis Patients.
Association Between Silent Myocardial Infarction and Long-Term Risk of Sudden Cardiac Death.
Association of prolonged QRS duration with ventricular tachyarrhythmias and sudden cardiac death in the Multicenter Automatic Defibrillator Implantation Trial II (MADIT-II).
Atrial fibrillation is associated with sudden cardiac death: a systematic review and meta-analysis.
Birthplace predicts risk for prehospital sudden cardiac death in middle-aged men who migrated to metropolitan area: The Helsinki Sudden Death Study.
Body Mass Index and Sudden Cardiac Death in Japanese Patients After Acute Myocardial Infarction: Data From the JCAD Study and HIJAMI-II Registry.
Brain-heart connection and the risk of heart attack.
Cardiorespiratory fitness and heart rate recovery predict sudden cardiac death independent of ejection fraction.
Catheter ablation to prevent sudden cardiac death.
Chronic Omega-3 Polyunsaturated Fatty Acid Treatment Variably Affects Cellular Repolarization in a Healed Post-MI Arrhythmia Model.
Clinical use of magnetic resonance imaging for the diagnosis of acute myocardial infarction in the survivors of cardiac arrest.
Clinical Use of Magnetic Resonance Imaging for the Diagnosis of Acute Myocardial Infarction in the Survivors of Cardiac Arrest.
Comparison of family history of sudden cardiac death in nonischemic and ischemic heart disease.
Comparison of risk profiles between survivors and victims of sudden cardiac death from an acute coronary event.
Coronary artery disease in athletes: An adverse effect of intense exercise?
Cost-effectiveness of in-home automated external defibrillators for individuals at increased risk of sudden cardiac death.
Daily peaks in the incidence of sudden cardiac death and fatal stroke in Niigata Prefecture.
Depression and risk of sudden cardiac death and coronary heart disease in women: results from the Nurses' Health Study.
Depressive symptoms and the risk of sudden cardiac death among the elderly.
Dietary alpha-linolenic acid intake and risk of sudden cardiac death and coronary heart disease.
Early Repolarization Pattern Associated with Sudden Cardiac Death: Long-Term Follow-Up in Patients with Chronic Heart Failure.
Effect of the antipsychotic drug haloperidol on arrhythmias during acute myocardial infarction in a porcine model.
Effects of angiotensin-converting enzyme inhibitor therapy on QT dispersion post acute myocardial infarction.
Electrocardiographic predictors of mortality and sudden cardiac death in patients with end stage renal disease on hemodialysis.
Elimination of allosteric modulation of myocardial KATP channels by ATP and protons in two Kir6.2 polymorphisms found in sudden cardiac death.
Epidemiology and genetics of ventricular fibrillation during acute myocardial infarction.
Family history and the risk of sudden cardiac death as a manifestation of an acute coronary event.
Fatty Acid desaturase gene variants, cardiovascular risk factors, and myocardial infarction in the costa rica study.
Forensic pathological investigation of myocardial hypoxia-inducible factor-1 alpha, erythropoietin and vascular endothelial growth factor in cardiac death.
Global burden of Sudden Cardiac Death and insights from India.
Heart rate variability as predictive factor for sudden cardiac death.
Histopathology of the conduction system in sudden death from coronary heart disease.
Implantable cardioverter defibrillators for the treatment of arrhythmias and cardiac resynchronisation therapy for the treatment of heart failure: systematic review and economic evaluation.
Implantable cardioverter-defibrillators: expanding indications and technologies.
Implantation of the automatic cardioverter-defibrillator.
Increased risk of sudden and non-sudden cardiovascular death in patients with atrial fibrillation/flutter following acute myocardial infarction.
Indications for an implantable cardioverter defibrillator (ICD).
Is High Serum LDL/HDL Cholesterol Ratio an Emerging Risk Factor for Sudden Cardiac Death? Findings from the KIHD Study.
Lambda-like ST segment elevation in acute myocardial infarction - a new risk marker for ventricular fibrillation? Three case reports.
Left atrial enlargement and NT-proBNP as predictors of sudden cardiac death in patients with heart failure.
Light-to-moderate alcohol consumption and risk of sudden cardiac death in women.
Long-term follow-up of survivors of prehospital sudden coronary death.
Long-term prognosis in patients with bifascicular block--the predictive value of noninvasive and invasive assessment.
Long-term subthreshold electrical stimulation of the left stellate ganglion and a canine model of sudden cardiac death.
Microparticles and sudden cardiac death due to coronary occlusion. The TIDE (Thrombus and Inflammation in sudden DEath) study.
Molecular autopsy in victims of inherited arrhythmias.
mRNA expression patterns in human myocardial tissue, pericardial fluid and blood, and its contribution to the diagnosis of cause of death.
Myocardial infarction in sickle cell disease.
Myocardial ischemia and ventricular tachycardia on continuous electrocardiographic monitoring and risk of cardiovascular outcomes after non-ST-segment elevation acute coronary syndrome (from the MERLIN-TIMI 36 Trial).
Neurohormonal intervention to reduce sudden cardiac death in heart failure: what is the optimal pharmacologic strategy?
No Association Between T-peak to T-end Interval on the Resting ECG and Long-Term Incidence of Ventricular Arrhythmias Triggering ICD Interventions.
Non-fatal cardiovascular events preceding sudden cardiac death in patients with an acute myocardial infarction complicated by heart failure: insights from the high-risk myocardial infarction database.
P75 neurotrophin receptor is a regulatory factor in sudden cardiac death with myocardial infarction.
Pathology of the myocardium and the conduction system in sudden coronary death.
Platelet collagen receptor GPIa (C807T/HPA-5) haplotype is not associated with an increased risk of fatal coronary events in middle-aged men.
Platelet glycoprotein Ibalpha HPA-2 Met/VNTR B haplotype as a genetic predictor of myocardial infarction and sudden cardiac death.
Postmortem mRNA expression patterns in left ventricular myocardial tissues and their implications for forensic diagnosis of sudden cardiac death.
Prediction and prevention of sudden cardiac death.
Prediction of arrhythmic events with positron emission tomography: PAREPET study design and methods.
Predictors of sudden cardiac death in high-risk patients following a myocardial infarction.
Prevention of sudden cardiac death with omega-3 fatty acids in patients with coronary heart disease: a meta-analysis of randomized controlled trials.
Prior myocardial infarction in the young: predisposes to a high relative risk but low absolute risk of a sudden cardiac death.
Prior myocardial infarction is the major risk factor associated with sudden cardiac death during downhill skiing.
Prospective study of sudden cardiac death among women in the United States.
Proteasome inhibition 1 h following ischemia protects GRK2 and prevents malignant ventricular tachyarrhythmias and SCD in a model of myocardial infarction.
Psychotropic medications and the risk of sudden cardiac death during an acute coronary event.
Racial and ethnic disparities in subjective cognitive decline: a closer look, United States, 2015-2018.
Racial differences in sudden cardiac death among hypertensive patients during antihypertensive therapy: The LIFE study.
Regression of electrocardiographic left ventricular hypertrophy during antihypertensive therapy and reduction in sudden cardiac death: the LIFE Study.
Relation of atrial and/or ventricular premature complexes on a two-minute rhythm strip to the risk of sudden cardiac death (the Atherosclerosis Risk in Communities [ARIC] study).
Relation of body mass index to sudden cardiac death and the benefit of implantable cardioverter-defibrillator in patients with left ventricular dysfunction after healing of myocardial infarction.
Relation of systemic blood pressure to sudden cardiac death.
Relationship Between Anemia and Sudden Cardiac Death in Patients with Severe Aortic Stenosis.
Relationship of Sudden Cardiac Death to New-Onset Atrial Fibrillation in Hypertensive Patients with Left Ventricular Hypertrophy.
Repolarization abnormalities and afterdepolarizations in a canine model of sudden cardiac death.
Respiratory sinus arrhythmia as a predictor of sudden cardiac death after myocardial infarction.
Risk and Protective Factors for Sudden Cardiac Death During Leisure Activities in the Mountains: An Update.
Risk Factor and Prediction Modeling for Sudden Cardiac Death in Women With Coronary Artery Disease.
Risk factors for sudden cardiac death in middle-aged British men.
Risk of sports: do we need a pre-participation screening for competitive and leisure athletes?
Role of omega-3 ethyl ester concentrate in reducing sudden cardiac death following myocardial infarction and in management of hypertriglyceridemia: An Indian consensus statement.
RR-QT interval trend covariability for sudden cardiac death risk stratification.
SCD following myocardial infarction - Predicting the unpredictable.
SCD leads to the development and progression of acute myocardial infarction through the AMPK signaling pathway.
Sports-related sudden cardiac deaths in the young population of Switzerland.
State-specific mortality from sudden cardiac death--United States, 1999.
Sudden Cardiac Death After Non-ST-Segment Elevation Acute Coronary Syndrome.
Sudden cardiac death athletes: a systematic review.
Sudden Cardiac Death in Patients With Atrial Fibrillation: Insights From the ENGAGE AF-TIMI 48 Trial.
Sudden cardiac death in patients with chronic coronary heart disease.
Sudden cardiac death in patients with silent myocardial ischemia after myocardial infarction (from the Swiss Interventional Study on Silent Ischemia Type II [SWISSI II]).
Sudden cardiac death in post myocardial infarction patients.
Sudden cardiac death in South India: Incidence, risk factors and pathology.
Sudden cardiac death in the young: the molecular autopsy and a practical approach to surviving relatives.
Sudden Cardiac Death Risk in Downhill Skiers and Mountain Hikers and Specific Prevention Strategies.
Sudden cardiac death risk prediction in heart failure with preserved ejection fraction.
Sudden Cardiac Death Risk Stratification - An Update.
Sudden cardiac death.
Sudden cardiac death: epidemiology, causes, and mechanisms.
Sudden coronary death in middle age and characteristics of its victims in Finland. A prospective population study.
Sudden death and its predictors in myocardial infarction survivors in an Indian population.
Sudden death in patients with chronic bifascicular block.
SVAD: A genetic database curates non-ischemic sudden cardiac death-associated variants.
T wave alternans and ventricular tachyarrhythmia risk stratification: a review.
T-wave alternans predicts mortality in a population undergoing a clinically indicated exercise test.
Temporal distribution of death among oncology patients: environmental links.
The anti-arrhythmic effects of n-3 PUFAs.
The automatic implantable defibrillator is the most realistic and cost-effective way of preventing sudden cardiac death.
The autonomic nervous system and ventricular arrhythmias in myocardial infarction and heart failure.
The European Myocardial Infarct Amiodarone Trial (EMIAT). EMIAT Investigators.
The prognostic value of haemodynamic parameters in the recovery phase of an exercise test. The Finnish Cardiovascular Study.
The risk of cardiovascular events during leisure time activities at altitude.
The Role of the Cardioversion Defibrillator in Post Myocardial Infarction Sudden Cardiac Death: A Systematic Review of Clinical Trials and Observational Studies.
The wearable cardioverter-defibrillator vest: Indications and ongoing questions.
Time-frequency analysis of ECG for late potentials in sudden cardiac death survivors and post-myocardial infarction patients.
Validation of the HCM Risk-SCD model in patients with hypertrophic cardiomyopathy following alcohol septal ablation.
Vascular histopathology and connective tissue ultrastructure in spontaneous coronary artery dissection: pathophysiological and clinical implications.
Ventricular tachycardia and sudden cardiac death.
Vitamin D deficiency is associated with sudden cardiac death, combined cardiovascular events, and mortality in haemodialysis patients.
Who should receive an implantable cardioverter-defibrillator after myocardial infarction?
[Autopsy pathological characteristics in coronary artery disease patients with or without sudden cardiac death].
[Characteristics of coronary artery involvement and probability of appropriate discharges of cardioverter-defibrillator implanted for primary prevention of sudden cardiac death].
[Impact of Myocardial Infarction and Abnormalities of Cardiac Conduction System on Sudden Cardiac Death].
[Primary prevention of sudden cardiac death implanted cardioverter defibrillator (ICD) versus antiarrhythmic drugs]
[Prognostic value of microvolt level T-wave alternans in patients at high risk of sudden cardiac death]
[Psychological and psychosocial factors in sudden cardiac death]
[Relationship between arrhythmia profile, left ventricular function and sudden death in the post-infarct period of patients resuscitated from heart arrest]
[Risk factors and prevention of sudden cardiac death in patients with ventricular tachycardia after myocardial infarct]
[Status of the adrenal medulla in various types of sudden cardiac death]
[Sudden Cardiac Death in Patients With Ischemic Heart Disease: From Mechanisms to Clinical Practice].
[Sudden cardiac death: state of the art]
[Wearable cardioverter-defibrillators: clinical experience and future perspectives].
Myocardial Ischemia
Activated cranial cervical cord neurons affect left ventricular infarct size and the potential for sudden cardiac death.
Association of early repolarization and sudden cardiac death during an acute coronary event.
Brief sympathetic activation precedes the development of ventricular tachycardia and ventricular fibrillation in hibernating myocardium.
Circular RNAs in Sudden Cardiac Death Related Diseases: Novel Biomarker for Clinical and Forensic Diagnosis.
Combined Effect of Sauna Bathing and Cardiorespiratory Fitness on the Risk of Sudden Cardiac Deaths in Caucasian Men: a Long-Term Prospective Cohort Study.
Congenital Coronary Artery Anomalies and Sudden Cardiac Death.
Coronary spasm during cardiac electrophysiological study following isoproterenol infusion.
Dissociation of hemodynamic and electrocardiographic indexes of myocardial ischemia in pigs with hibernating myocardium and sudden cardiac death.
Dystrophin and metalloproteinase 9 in myocardial ischemia: A post-mortem immunohistochemical study.
Early autonomic and repolarization abnormalities contribute to lethal arrhythmias in chronic ischemic heart failure: characteristics of a novel heart failure model in dogs with postmyocardial infarction left ventricular dysfunction.
Epidemiology and stratification of risk for sudden cardiac death.
Exercise heart rate reserve and recovery as risk factors for sudden cardiac death.
Hypertension, left ventricular hypertrophy, and sudden cardiac death.
Hypertension, left ventricular hypertrophy, and sudden death.
Implantable cardioverter defibrillators. Prophylactic use: an evidence-based analysis.
Ischemic Heart Disease Related Sudden Cardiac Death in Autopsied Cases: An Egyptian perspective.
Joint effect of blood pressure and C-reactive protein and the risk of sudden cardiac death: A prospective cohort study.
Lethal immunoglobulins: Autoantibodies and sudden cardiac death.
Lipoprotein(a) and risk of sudden cardiac death in middle-aged Finnish men: A new prospective cohort study.
Marine n-3 fatty acids, wine intake, and heart rate variability in patients referred for coronary angiography.
Mechanisms of sudden cardiac death.
Metabolic risk factors associated with sudden cardiac death (SCD) during acute myocardial ischemia.
Myocardial Infarction in Sickle Cell Disease: Use of Translational Imaging to Diagnose an Under-Recognized Problem.
Myocardial ischemia and right ventricular dysfunction in adult patients with sickle cell disease.
Outcomes of patients admitted with ventricular arrhythmias and sudden cardiac death in the United States.
Overview of completed sudden death trials: European experience.
PAI-I 4G/5G polymorphism and sudden cardiac death in patients with coronary artery disease.
Pathology of the myocardium and the conduction system in sudden coronary death.
Post-mortem CMR in a model of sudden death due to myocardial ischemia: validation with connexin-43.
Postmortem imaging of sudden cardiac death.
Postmortem mRNA expression patterns in left ventricular myocardial tissues and their implications for forensic diagnosis of sudden cardiac death.
Racial differences in sudden cardiac death among hypertensive patients during antihypertensive therapy: The LIFE study.
Relationship of Sudden Cardiac Death to New-Onset Atrial Fibrillation in Hypertensive Patients with Left Ventricular Hypertrophy.
Risk factors for sudden cardiac death in middle-aged British men.
Role of antiarrhythmic therapy in patients at risk for sudden cardiac death: an evidence-based review.
Strategies for the prevention and treatment of sudden cardiac death.
Sudden Cardiac and Noncardiac Death in Sports: Epidemiology, Causes, Pathogenesis, and Prevention.
Sudden cardiac death and myocardial ischemia indicators: a comparative study of four immunohistochemical markers.
Sudden cardiac death athletes: a systematic review.
Sudden cardiac death during physical exercise: Characteristics of victims and autopsy findings.
Sudden Cardiac Death in Adult Congenital Heart Disease.
Sudden cardiac death in children and young adults without structural heart disease: a comprehensive review.
Sudden Cardiac Death in Ischemic Heart Disease: From Imaging Arrhythmogenic Substrate to Guiding Therapies.
Sudden cardiac death in patients with hypertrophic cardiomyopathy: from bench to bedside with an emphasis on genetic markers.
Sudden cardiac death in patients with nonischemic cardiomyopathy.
Sudden cardiac death in patients with silent myocardial ischemia after myocardial infarction (from the Swiss Interventional Study on Silent Ischemia Type II [SWISSI II]).
Sudden Cardiac Death in Women With Suspected Ischemic Heart Disease, Preserved Ejection Fraction, and No Obstructive Coronary Artery Disease: A Report From the Women's Ischemia Syndrome Evaluation Study.
Sudden cardiac death: A comparative review of humans, dogs and cats.
Sudden coronary death in the young: Evidence of contractile phenotype of smooth muscle cells in the culprit atherosclerotic plaque.
The effect of coronary bypass graft surgery for the prevention of sudden cardiac death: recurrent episodes after ICD implantation and review of literature.
Tools for risk stratification of sudden cardiac death: A review of the literature in different patient populations.
Ventricular Arrhythmias Among Implantable Cardioverter-Defibrillator Recipients for Primary Prevention: Impact of Chronic Total Coronary Occlusion (VACTO Primary Study).
[Acute cardiac death in chronic-ischemic heart disease (CIHD)]
[In Process Citation]
[Personal Telemonitoring: Perspectives of Development in Arhythmology and Cardiology].
[Pharmacological possibilities for the prevention of complications following myocardial infarction]
[Sudden cardiac death in diabetes mellitus].
[Sudden cardiac death: state of the art]
[The application of biochemical indexes detecting in sudden cardiac death in forensic autopsy]
Myocarditis
A Challenging Case Of Ventricular Arrhythmia In A Patient With Myocarditis: ICD Yes/No After Ablation.
Arrhythmogenic right ventricular cardiomyopathy and sudden cardiac death in young Koreans.
Circular RNAs in Sudden Cardiac Death Related Diseases: Novel Biomarker for Clinical and Forensic Diagnosis.
Electrocardiograms in athletes: interpretation and diagnostic accuracy.
Forensic Pathological Study of 1656 Cases of Sudden Cardiac Death in Southern China.
Implantable cardioverter-defibrillator and wait-list outcomes in pediatric patients awaiting heart transplantation.
Is Exercise Helpful or Harmful in Dealing With Specific Arrhythmia.
Ischemic Heart Disease Related Sudden Cardiac Death in Autopsied Cases: An Egyptian perspective.
Lethal immunoglobulins: Autoantibodies and sudden cardiac death.
Life threatening parvovirus B19 and herpes simplex virus associated acute myocardial dysfunction in a child with homozygous sickle cell disease.
Myocarditis in the Athlete: Arrhythmogenic Substrates, Clinical Manifestations, Management, and Eligibility Decisions.
Retrospective analysis of 769 cases of sudden cardiac death from 2006 to 2015: a forensic experience in China.
Right coronary anomaly in a patient with myocarditis and cardiac arrest: a case report.
Secondary Prevention of Potentially Life-Threatening Arrhythmia Using Implantable Cardioverter Defibrillators in Patients with Biopsy-Proven Viral Myocarditis and Preserved Ejection Fraction.
Sudden cardiac death and tuberculosis - How much do we know?
Sudden cardiac death caused by myocarditis in persons aged 1-49 years: a nationwide study of 14?294 deaths in Denmark.
Sudden cardiac death from structural heart diseases in adults: imaging findings with cardiovascular computed tomography and magnetic resonance.
Sudden cardiac death in football players: Towards a new pre-participation algorithm.
Sudden cardiac death in patients with myocarditis: Evaluation, risk stratification, and management.
Sudden cardiac death in young athletes; a literature review and special considerations in Asia.
The autopsy study of 553 cases of sudden cardiac death in Chinese adults.
The injury-vasospasm hypothesis of ischemic heart disease, revisited.
What Is the Arrhythmic Substrate in Viral Myocarditis? Insights from Clinical and Animal Studies.
[Arrhythmogenic dysplasia of right ventricle: pathogenesis, genetic markers, clinical presentation, clinical example]
[Sudden cardiac death in women].
Myoclonic Epilepsies, Progressive
Cognitive impairment in spinocerebellar degeneration.
Myositis
Juvenile polymyositis with unremitting pain and progressive loss of motor and bulbar function on a background of sickle cell disease.
Myotonic Dystrophy
Sudden cardiac death in neuromuscular disorders.
Neoplasm Metastasis
HER2/neu negative salivary duct carcinoma of parotid: A case with forty months recurrence free follow up.
Omega-3 polyunsaturated fatty acids suppress metastatic features of human cholangiocarcinoma cells by suppressing twist.
Prognostic factor identification by screening changes in differentially expressed genes in oral squamous cell carcinoma.
Squamous Cell Differentiation in Metastatic Papillary Thyroid Carcinoma: Metaplastic Reversion or Progression?
Stearoyl-CoA desaturase-1 promotes colorectal cancer metastasis in response to glucose by suppressing PTEN.
Sulforaphene inhibits esophageal cancer progression via suppressing SCD and CDH3 expression, and activating the GADD45B-MAP2K3-p38-p53 feedback loop.
Neoplasms
17?-estradiol induces stearoyl-CoA desaturase-1 expression in estrogen receptor-positive breast cancer cells.
A Method to Identify California's Sickle-Cell Disease Population and its Linkage to the California Cancer Registry.
A more physiological approach to lipid metabolism alterations in cancer: CRC-like organoids assessment.
A novel armed oncolytic measles vaccine virus for the treatment of cholangiocarcinoma.
A Novel Ferroptosis-Related Gene Model for Overall Survival Predictions of Bladder Urothelial Carcinoma Patients.
Accelerated bottom-up drug design platform enables the discovery of novel stearoyl-CoA desaturase 1 inhibitors for cancer therapy.
Airway Inflammation and Lung Function in Sickle Cell Disease.
Altered expression of genes in adipose tissues associated with reduced fat mass in patients with pancreatic cancer.
Analysis of the stearoyl-CoA desaturase system in the Morris hepatoma 7288C and 7288CTC.
Assessing responsiveness over time of the PROMIS(®) pediatric symptom and function measures in cancer, nephrotic syndrome, and sickle cell disease.
Attitudes and beliefs of relatives of patients with sickle cell disease.
Baseline TP53 mutations in Adults with SCD developing Myeloid Malignancy following Hematopoietic Cell Transplantation.
Benign cardiac tumours associated with sudden death.
Biomarkers of inflammation, growth factor, and coagulation activation in patients with sickle cell disease.
Bladder carcinoma with shadow cell differentiation: a case report with immunohistochemical analyses.
Cancer cell dependence on unsaturated fatty acids implicates stearoyl-CoA desaturase as a target for cancer therapy.
Cancer death is related to high palmitoleic acid in serum and to polymorphisms in the SCD-1 gene in healthy Swedish men.
Cancer incidence rate and mortality rate in sickle cell disease patients at Howard University Hospital: 1986-1995.
Cancer specific survival in patients with sickle cell disease.
Canonical Wnt Signaling Remodels Lipid Metabolism in Zebrafish Hepatocytes following Ras Oncogenic Insult.
Central venous catheter complications in sickle cell disease.
Clinical and biochemical relevance of monounsaturated fatty acid metabolism targeting strategy for cancer stem cell elimination in colon cancer.
Cobalamin (vitamin B(12)) in subacute combined degeneration and beyond: traditional interpretations and novel theories.
Coexistence of Lambert-Eaton myasthenic syndrome and subacute cerebellar degeneration: differential effects of treatment.
Crystal structure of human stearoyl-coenzyme A desaturase in complex with substrate.
Design, radiosynthesis, and evaluation of radiotracers for positron emission tomography imaging of stearoyl-CoA desaturase-1.
Development of a New Adult Sickle Cell Disease Center Within an Academic Cancer Center: Impact on Hospital Utilization Patterns and Care Quality.
Dietary alpha-linolenic acid intake and risk of sudden cardiac death and coronary heart disease.
Differences in Gut Microbiome in Hospitalized Immunocompetent vs. Immunocompromised Children, Including Those With Sickle Cell Disease.
Differences in Sensory Pain, Expectation, and Satisfaction Reported by Outpatients with Cancer or Sickle Cell Disease.
Differential effects of rexinoids and thiazolidinediones on metabolic gene expression in diabetic rodents.
Direct and maternal n-3 long-chain polyunsaturated fatty acid supplementation improved triglyceridemia and glycemia through the regulation of hepatic and muscle sphingolipid synthesis in offspring hamsters fed a high-fat diet.
Discovery of Cytochrome P450 4F11 Activated Inhibitors of Stearoyl Coenzyme A Desaturase.
Discovery of tumor-specific irreversible inhibitors of stearoyl CoA desaturase.
Downregulation of CPT2 promotes tumorigenesis and chemoresistance to cisplatin in hepatocellular carcinoma.
Effects of adenoviral gene transfer of C. elegans n-3 fatty acid desaturase on the lipid profile and growth of human breast cancer cells.
Effects of Natural Products on Fructose-Induced Nonalcoholic Fatty Liver Disease (NAFLD).
Electroacupuncture in conscious free-moving mice reduces pain by ameliorating peripheral and central nociceptive mechanisms.
Endogenously synthesized n-3 fatty acids in fat-1 transgenic mice prevent melanoma progression by increasing E-cadherin expression and inhibiting ?-catenin signaling.
Evaluation of various biomarkers as potential mediators of the association between ?5 desaturase, ?6 desaturase, and stearoyl-CoA desaturase activity and incident type 2 diabetes in the European Prospective Investigation into Cancer and Nutrition-Potsdam Study.
Evidence for an alternative fatty acid desaturation pathway increasing cancer plasticity.
Exosome-mediated delivery of SCD-1 siRNA promoted the death of anaplastic thyroid carcinoma cells via regulating ROS level.
Expression of SCD and FADS2 Is Lower in the Necrotic Core and Growing Tumor Area than in the Peritumoral Area of Glioblastoma Multiforme.
Extensive Bone Marrow Necrosis: Initial Presentation in Sickle Cell Anemia-A Case Report and Review of the Literature.
FADS1 is a Prognostic Biomarker in Bladder Cancer: A Study Based on TCGA Data.
Fatty Acid Composition of Tissue Cultured Breast Carcinoma and the Effect of Stearoyl-CoA Desaturase 1 Inhibition.
Fenretinide Induces Ubiquitin-Dependent Proteasomal Degradation of Stearoyl-CoA Desaturase in Human Retinal Pigment Epithelial Cells.
Genistein downregulates de novo lipid synthesis and impairs cell proliferation in human lung cancer cells.
Hepatic SirT1-Dependent Gain of Function of Stearoyl-CoA Desaturase-1 Conveys Dysmetabolic and Tumor Progression Functions.
Hepatocyte differentiation of human induced pluripotent stem cells is modulated by stearoyl-CoA desaturase 1 activity.
High Expression of Stearoyl-CoA Desaturase 1 Predicts Poor Prognosis in Patients with Clear-Cell Renal Cell Carcinoma.
High stearoyl-CoA desaturase protein and activity levels in simian virus 40 transformed-human lung fibroblasts.
Hydroxyurea for the treatment of sickle cell disease.
Identification of Ras-related nuclear protein, targeting protein for xenopus kinesin-like protein 2, and stearoyl-CoA desaturase 1 as promising cancer targets from an RNAi-based screen.
Immunohistochemical analysis of 11-beta-hydroxysteroid dehydrogenase type 2 and glucocorticoid receptor in subclinical Cushing's disease due to pituitary macroadenoma.
In vitro and in vivo antitumor activities of T-3764518, a novel and orally available small molecule stearoyl-CoA desaturase 1 inhibitor.
In vivo production of type 1 cytokines in healthy sickle cell disease patients.
Incidence and other epidemiological characteristics of sudden cardiac death in northwest Greece.
Incidence and predictors of sudden cardiac death after heart transplantation: A systematic review and meta-analysis.
Increased expression of the gene encoding stearoyl-CoA desaturase 1 in human bladder cancer.
Increased FNDC5/Irisin expression in human hepatocellular carcinoma.
Increased lipogenesis is critical for self-renewal and growth of breast cancer stem cells: Impact of omega-3 fatty acids.
Inhibition of fatty acid desaturation is detrimental to cancer cell survival in metabolically compromised environments.
Inhibition of stearoyl CoA desaturase-1 activity suppresses tumour progression and improves prognosis in human bladder cancer.
Inhibition of Stearoyl-CoA Desaturase 1 expression in human lung adenocarcinoma cells impairs tumorigenesis.
Inhibition of stearoyl-CoA desaturase 1 expression induces CHOP-dependent cell death in human cancer cells.
Inhibition of Stearoyl-CoA desaturase 1 reverts BRAF and MEK inhibition-induced selection of cancer stem cells in BRAF-mutated melanoma.
Inhibition of Stearoyl-CoA Desaturase Induces the Unfolded Protein Response in Pancreatic Tumors and Suppresses Their Growth.
Inhibition of stearoylCoA desaturase activity blocks cell cycle progression and induces programmed cell death in lung cancer cells.
Inhibition of stearoylCoA desaturase-1 inactivates acetyl-CoA carboxylase and impairs proliferation in cancer cells: role of AMPK.
Integrated Metabolite and Gene Expression Profiles Identify Lipid Biomarkers Associated With Progression of Hepatocellular Carcinoma and Patient Outcomes.
Lauroylated Histidine-Enriched S413-PV Peptide as an Efficient Gene Silencing Mediator in Cancer Cells.
Lipid metabolism in cancer: A systematic review.
Lipogenesis in cancer progression (review).
Long noncoding RNA UPAT promotes colon tumorigenesis by inhibiting degradation of UHRF1.
Loss of mitochondrial aconitase promotes colorectal cancer progression via SCD1-mediated lipid remodeling.
Loss of stearoyl-CoA desaturase expression is a frequent event in prostate carcinoma.
Lung carcinoma-associated atypical adenomatoid hyperplasia, squamous cell dysplasia, and chromosome alterations in non-neoplastic bronchial mucosa.
Lung fibroblasts promote metastatic colonization through upregulation of stearoyl-CoA desaturase 1 in tumor cells.
Malignancy in patients with sickle cell disease.
Malignant haemangioendothelioma of bone in a HbSC disease patient--a case report.
Management of Hodgkin Lymphoma in a Sickle Cell Patient: A Case Report.
Maternal supplementation with n-3 long chain polyunsaturated fatty acids during perinatal period alleviates the metabolic syndrome disturbances in adult hamster pups fed a high-fat diet after weaning.
Mechanisms of stearoyl CoA desaturase inhibitor sensitivity and acquired resistance in cancer.
Melanoma tumor growth is accelerated in a mouse model of sickle cell disease.
Modulation of de Novo Lipogenesis Improves Response to Enzalutamide Treatment in Prostate Cancer.
MR imaging features and tumor biomarkers of screen-detected and non-screen detected breast cancers: preliminary results of a comparative study.
Multihormonal pituitary adenoma concomitant with Pit-1 and Tpit lineage cells causing acromegaly associated with subclinical Cushing's disease: a case report.
n-3 Polyunsaturated fatty acids for the management of alcoholic liver disease: A critical review.
Nobiletin improves obesity and insulin resistance in high-fat diet-induced obese mice.
OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY FINDINGS OF DEEP CAPILLARY PLEXUS MICROISCHEMIA AFTER INTRAVENOUS CHEMOTHERAPY FOR RETINOBLASTOMA.
Palmitic acid (16:0) competes with omega-6 linoleic and omega-3 ?-linolenic acids for FADS2 mediated ?6-desaturation.
Parents' assessment of risk in sickle cell disease treatment with hydroxyurea.
Phenotype specific analyses reveal distinct regulatory mechanism for chronically activated p53.
Pivotal role of human stearoyl-CoA desaturases (SCD1 and 5) in breast cancer progression: oleic acid-based effect of SCD1 on cell migration and a novel pro-cell survival role for SCD5.
Plasma levels of TNF-alpha in sickle cell patients receiving hydroxyurea.
Platyphylloside Isolated From Betula platyphylla Inhibit Adipocyte Differentiation and Induce Lipolysis Via Regulating Adipokines Including PPAR? in 3T3-L1 Cells.
Positive feedback loop and synergistic effects between hypoxia-inducible factor-2? and stearoyl-CoA desaturase-1 promote tumorigenesis in clear cell renal cell carcinoma.
Prevention of venous thromboembolism in gynecological cancer patients undergoing major abdominopelvic surgery: A systematic review and network meta-analysis.
Progestin modulates the lipid profile and sensitivity of breast cancer cells to docetaxel.
Prognostic factor identification by screening changes in differentially expressed genes in oral squamous cell carcinoma.
Prostate cancer gene expression signature of patients with high body mass index.
Prostate tumor growth can be modulated by dietarily targeting the 15-lipoxygenase-1 and cyclooxygenase-2 enzymes.
Protective effect of Codonopsis lanceolata root extract against alcoholic fatty liver in the rat.
Psychological distress among adult cancer survivors: importance of survivorship care plan.
Psychosocial burden of sickle cell disease on caregivers in a Nigerian setting.
RA-XII Suppresses the Development and Growth of Liver Cancer by Inhibition of Lipogenesis via SCAP-dependent SREBP Supression.
Raised neutrophil phospholipase A2 activity and defective priming of NADPH oxidase and phospholipase A2 in sickle cell disease.
Reflections of Healthcare Experiences of African Americans With Sickle Cell Disease or Cancer: A Qualitative Study.
Regulation of gene expression by insulin and tumor necrosis factor alpha in 3T3-L1 cells. Modulation of the transcription of genes encoding acyl-CoA synthetase and stearoyl-CoA desaturase-1.
Regulation of stearoyl-CoA desaturase expression.
Renal abnormalities in sickle cell disease.
Resveratrol Improves Hepatic Redox Status and Lipid Balance of Neonates with Intrauterine Growth Retardation in a Piglet Model.
Risk Stratification of High-grade Prostate Cancer Treated with Antegrade Radical Prostatectomy with Intended Wide Resection.
SCD in the world, Europe, Bosnia and Herzegovina and Mostar.
SCD1 Expression Is Dispensable for Hepatocarcinogenesis Induced by AKT and Ras Oncogenes in Mice.
SCD1 negatively regulates autophagy-induced cell death in human hepatocellular carcinoma through inactivation of the AMPK signaling pathway.
SCD1, autophagy and cancer: implications for therapy.
SCD5 restored expression favors differentiation and epithelial-mesenchymal reversion in advanced melanoma.
Self-reported chemotherapy-related cognitive impairment compared with cognitive complaints following menopause.
Sequential development of human herpes virus 8-positive diffuse large B-cell lymphoma and chronic myelomonocytic leukemia in a 59 year old female patient with hemoglobin SC disease.
Serum Levels of Soluble CD 30 and Their Relationship to Tumour Burden and Prognosis in Patients with Hodgkin's Disease.
Serum levels of substance P are elevated in patients with sickle cell disease and increase further during vaso-occlusive crisis.
Shadow cell differentiation in endometrioid carcinomas of the uterus. Its frequent occurrence and beta-catenin expression.
Sickle cell anemia and hematological neoplasias.
Significantly increased monounsaturated lipids relative to polyunsaturated lipids in six types of cancer microenvironment are observed by mass spectrometry imaging.
Sleep and Pain in Pediatric Illness: A Conceptual Review.
Social interactions between children with cancer or sickle cell disease and their peers: teacher ratings.
Spatial modeling of prostate cancer metabolic gene expression reveals extensive heterogeneity and selective vulnerabilities.
Stearoyl CoA desaturase (SCD) facilitates proliferation of prostate cancer cells through enhancement of androgen receptor transactivation.
Stearoyl CoA Desaturase Is Essential for Regulation of Endoplasmic Reticulum Homeostasis and Tumor Growth in Glioblastoma Cancer Stem Cells.
Stearoyl CoA Desaturase Regulates Ferroptosis in Ovarian Cancer Offering New Therapeutic Perspectives.
Stearoyl-CoA desaturase 1 (SCD1) facilitates the growth and anti-ferroptosis of gastric cancer cells and predicts poor prognosis of gastric cancer.
Stearoyl-CoA desaturase 1 and paracrine diffusible signals have a major role in the promotion of breast cancer cell migration induced by cancer-associated fibroblasts.
Stearoyl-CoA Desaturase 1 as a Therapeutic Target for the Treatment of Cancer.
Stearoyl-CoA desaturase 1 is a novel molecular therapeutic target for clear cell renal cell carcinoma.
Stearoyl-CoA desaturase activity in mammary adenocarcinomas carried by C3H mice.
Stearoyl-CoA desaturase activity modulates the activation of epidermal growth factor receptor in human lung cancer cells.
Stearoyl-CoA desaturase and tumorigenesis.
Stearoyl-CoA desaturase enzyme 1 inhibition reduces glucose utilization for de novo fatty acid synthesis and cell proliferation in 3T3-L1 adipocytes.
Stearoyl-CoA desaturase inhibitors: update on patented compounds.
Stearoyl-CoA desaturase is involved in the control of proliferation, anchorage-independent growth, and survival in human transformed cells.
Stearoyl-CoA Desaturase Promotes Liver Fibrosis and Tumor Development in Mice via a Wnt Positive-Signaling Loop by Stabilization of Low-Density Lipoprotein-Receptor-Related Proteins 5 and 6.
Stearoyl-CoA desaturase-1 and adaptive stress signaling.
Stearoyl-CoA Desaturase-1 Attenuates the High Shear Force Damage Effect on Human MG63 Osteosarcoma Cells.
Stearoyl-CoA Desaturase-1 Enzyme Inhibition by Grape Skin Extracts Affects Membrane Fluidity in Human Colon Cancer Cell Lines.
Stearoyl-CoA desaturase-1 mediated cell apoptosis in colorectal cancer by promoting ceramide synthesis.
Stearoyl-CoA desaturase-1: a novel key player in the mechanisms of cell proliferation, programmed cell death and transformation to cancer.
Stearoyl-CoA Desaturase: A Vital Checkpoint in the Development and Progression of Obesity.
Stearoyl-CoA-desaturase-1 regulates gastric cancer stem-like properties and promotes tumour metastasis via Hippo/YAP pathway.
Sterculic Acid Alters Adhesion Molecules Expression and Extracellular Matrix Compounds to Regulate Migration of Lung Cancer Cells.
Sterol regulatory element-binding protein 1 inhibitors decrease pancreatic cancer cell viability and proliferation.
Structure-based virtual screening of natural products as potential stearoyl-coenzyme a desaturase 1 (SCD1) inhibitors.
Subcutaneous panniculitis-like T-cell lymphoma in a 25-year-old male patient with sickle cell disease.
Subjective cognitive dysfunction in breast cancer patients: a systematic review.
Targeting Mac-1-mediated leukocyte-RBC interactions uncouples the benefits for acute vaso-occlusion and chronic organ damage.
Targeting Peroxisome Proliferator-Activated Receptor ? to Increase Estrogen-Induced Apoptosis in Estrogen-Deprived Breast Cancer Cells.
Targeting stearoyl-CoA desaturase 1 to repress endometrial cancer progression.
The Cellie Coping Kit for Sickle Cell Disease: Initial acceptability and feasibility.
The Evolving Pharmacotherapeutic Landscape for the Treatment of Sickle Cell Disease.
The fatty acid desaturation index of blood lipids, as a biomarker of hepatic stearoyl-CoA desaturase expression, is a predictive factor of breast cancer risk.
The Hypoxic Microenvironment Induces Stearoyl-CoA Desaturase-1 Overexpression and Lipidomic Profile Changes in Clear Cell Renal Cell Carcinoma.
The opinion of caregivers on aspects of schizophrenia and major affective disorders in a Nigerian setting.
The role of oncology nurses in the care of adults with sickle cell disease.
The Role of Promyelocytic Leukemia Protein in Steatosis-Associated Hepatic Tumors Related to Chronic Hepatitis B virus Infection.
The role of stearoyl-coenzyme A desaturase 1 in clear cell renal cell carcinoma.
The Stearoyl-CoA Desaturase-1 (Desat1) in Drosophila cooperated with Myc to Induce Autophagy and Growth, a Potential New Link to Tumor Survival.
The use of stimulant medication to treat neurocognitive deficits in patients with pediatric cancer, traumatic brain injury, and sickle cell disease: a review.
Transition of care in pediatric oncohematology: a systematic literature review.
Treatment and outcomes of hepatocellular carcinoma in patients with Sickle cell disease: a population-based study in the U.S.
Tumor biology of non-metastatic stages of clear cell renal cell carcinoma; overexpression of stearoyl desaturase-1, EPO/EPO-R system and hypoxia-related proteins.
Tumor burden and serum level of soluble CD25, CD8, CD23, CD54 and CD44 in non-Hodgkin's lymphoma.
Tumor necrosis factor alpha in children with sickle cell disease in stable condition.
Tumor resistance to ferroptosis driven by Stearoyl-CoA Desaturase-1 (SCD1) in cancer cells and Fatty Acid Biding Protein-4 (FABP4) in tumor microenvironment promote tumor recurrence.
Tumor-Activated Benzothiazole Inhibitors of Stearoyl-CoA Desaturase.
Tumor-Associated Stromal Cellular Density as a Predictor of Recurrence and Mortality in Breast Cancer: Results from Ethnically Diverse Study Populations.
TXNIP/VDUP1 attenuates steatohepatitis via autophagy and fatty acid oxidation.
Unusual SCD in cancer cells: a phenomenon related to decreased BrdU incorporation?
Using the Method of "Optical Biopsy" of Prostatic Tissue to Diagnose Prostate Cancer.
[Expression of c-myc, c-erbB-2, insulin-like growth factor II andepidermal growth factor receptor in hepatitis B, cirrhosis and hepatocellular carcinoma]
Nephrotic Syndrome
Atypical presentation of acute post-infectious glomerulonephritis in patients with sickle cell disease: report of two cases.
Life threatening parvovirus B19 and herpes simplex virus associated acute myocardial dysfunction in a child with homozygous sickle cell disease.
Nephrotic syndrome on sickle cell disease: the impact of Hydroxyurea.
Seizures risk factors in sickle cell disease. The cooperative study of sickle cell disease.
Nervous System Malformations
Severe spondylocostal dysostosis associated with other congenital anomalies: a clinical/epidemiologic analysis and description of ten cases from the Spanish registry.
Neural Tube Defects
Spondylocostal dysostosis associated with right-sided polythelia, right-sided rib deformity and meningocoele: Case report with review of literature.
Neuralgia
A QST-based Pain Phenotype in Adults With Sickle Cell Disease: Sensitivity and Specificity of Quality Descriptors.
Early insights into the neurobiology of pain in sickle cell disease: A systematic review of the literature.
Gabapentin alleviates chronic spontaneous pain and acute hypoxia-related pain in a mouse model of sickle cell disease.
Health-related quality of life and neuropathic pain in sickle cell disease in Jamaica.
Impact of neuropathic pain on quality of life in adults with sickle cell disease: observational study.
Interventions for treating neuropathic pain in people with sickle cell disease.
Management of Sickle Cell Pain Using Pregabalin: A Pilot Study.
Neuropathic Pain and Sickle Cell Disease: a Review of Pharmacologic Management.
Neuropathic Pain in Children with Sickle Cell Disease: The Hidden Side of the Vaso-Occlusive Crisis.
Neuropathic pain in individuals with sickle cell disease.
Neuropathic pain in patients with sickle cell disease.
Neuropathic pain in patients with sickle cell disease: a cross-sectional study assessing teens and young adults.
Neuropathic pain in sickle cell disease: measurement and management.
Neuropathic pain is associated with poor health-related quality of life in adolescents with sickle cell disease: A preliminary report.
Neuropathic Pain Screening: Construct Validity in Patients With Sickle Cell Disease.
Safety and Utility of Quantitative Sensory Testing among Adults with Sickle Cell Disease: Indicators of Neuropathic Pain?
Screening for neuropathic pain in patients with sickle cell disease: is a single assessment scale sufficient?
Sensitivities to Thermal and Mechanical Stimuli: Adults with Sickle Cell Disease Compared to Healthy, Pain-free African American Controls.
Sensory and Thermal Quantitative Testing in Children With Sickle Cell Disease.
The use of neuropathic pain drugs in children with sickle cell disease is associated with older age, female sex, and longer length of hospital stay.
Neurobehavioral Manifestations
Subjective cognitive decline in diabetes: Associations with psychological, sleep, and diabetes-related factors.
Neuroblastoma
CLN3P, the Batten's disease protein, is a novel palmitoyl-protein Delta-9 desaturase.
SCD Inhibition Protects from ?-Synuclein-Induced Neurotoxicity But Is Toxic to Early Neuron Cultures.
The Role of MYCN in Symmetric vs. Asymmetric Cell Division of Human Neuroblastoma Cells.
Neurodegenerative Diseases
Brain connectivity and metacognition in persons with subjective cognitive decline (COSCODE): rationale and study design.
Cognitive frailty, a novel target for the prevention of elderly dependency.
Design and first baseline data of the DZNE multicenter observational study on predementia Alzheimer's disease (DELCODE).
Smaller medial temporal lobe volumes in individuals with subjective cognitive decline and biomarker evidence of Alzheimer's disease-Data from three memory clinic studies.
The characterisation of subjective cognitive decline.
Neuroinflammatory Diseases
Analysis of hippocampal subfields in sickle cell disease using ultrahigh field MRI.
Role of age and neuroinflammation in the mechanism of cognitive deficits in sickle cell disease.
SC411 treatment can enhance survival in a mouse model of sickle cell disease.
Neuroleptic Malignant Syndrome
[Study on argyrophilic inclusions of multisystem atrophy (Oppenheimer)]
Neurologic Manifestations
Anesthesia for cerebral revascularization for adult moyamoya syndrome associated with sickle cell disease.
Carotid artery duplex scanning in preoperative assessment for coronary artery revascularization: the association between peripheral vascular disease, carotid artery stenosis, and stroke.
Co-occurrence of Chiari malformations and sickle cell disease-a diagnostic dilemma: a report of 4 cases and review of literature.
Cranial involvement in sickle cell disease.
Diffuse skull base/cervical fusion syndromes in two siblings with spondylocostal dysostosis syndrome: analysis via three dimensional computed tomography scanning.
Low cobalamin levels in African Americans with and without sickle cell disease.
Peripheral nervous system involvement in patients with sickle cell disease.
Role of positron emission tomography in determining the extent of CNS ischemia in patients with sickle cell disease.
Spontaneous dissection of the carotid and vertebral arteries: the 10-year UCSD experience.
Neuronal Ceroid-Lipofuscinoses
Intermediate levels of neuronal palmitoyl-protein Delta-9 desaturase in heterozygotes for murine Batten disease.
Neutropenia
Hydroxyurea for the treatment of sickle cell disease.
Nocturnal Enuresis
Cystatin C, Beta2 Microglobulin, N-Acetyl-beta-D-glucosaminidase, Retinol-Binding Protein, and Endothelin 1 Levels in the Evaluation of Sickle Cell Disease Nephropathy.
Nocturnal enuresis and psychosocial problems in pediatric sickle cell disease and sibling controls.
Nocturnal enuresis in pediatric sickle cell disease.
Nocturnal enuresis in sickle cell disease and thalassemia major: associated factors in a clinical sample.
Nocturnal enuresis in sickle cell disease.
Nocturnal Enuresis in Sickle Cell: Sociodemographic, Medical, and Quality of Life Factors.
Overactive bladder in adults with sickle cell disease.
Sickle cell nephropathy: challenging the conventional wisdom.
Non-alcoholic Fatty Liver Disease
A novel inhibitor of stearoyl-CoA desaturase-1 attenuates hepatic lipid accumulation, liver injury and inflammation in model of nonalcoholic steatohepatitis.
A return to ad libitum feeding following caloric restriction promotes hepatic steatosis in hyperphagic OLETF rats.
Amelioration by Idesia polycarpa Maxim. var. vestita Diels. of Oleic Acid-Induced Nonalcoholic Fatty Liver in HepG2 Cells through Antioxidant and Modulation of Lipid Metabolism.
Biosynthesis and bioavailability of long-chain polyunsaturated fatty acids in non-alcoholic fatty liver disease.
Dietary polyunsaturated fatty acids mediate the inverse association of stearoyl-CoA desaturase activity with the risk of fatty liver in dyslipidaemic individuals.
Downregulated microRNA-130b-5p prevents lipid accumulation and insulin resistance in a murine model of nonalcoholic fatty liver disease.
Effect of skin-capsular distance on controlled attenuation parameter for diagnosing liver steatosis in patients with nonalcoholic fatty liver disease.
Effects of Natural Products on Fructose-Induced Nonalcoholic Fatty Liver Disease (NAFLD).
Fatty Acid Desaturase Involvement in Non-Alcoholic Fatty Liver Disease Rat Models: Oxidative Stress Versus Metalloproteinases.
Fatty liver disease in persons with HIV infection.
Fatty Liver Is Associated with Transcriptional Downregulation of Stearoyl-CoA Desaturase and Impaired Protein Dimerization.
Food-drug interaction: Anabolic steroids aggravate hepatic lipotoxicity and nonalcoholic fatty liver disease induced by trans fatty acids.
Geniposide and Chlorogenic Acid Combination Improves Non-Alcoholic Fatty Liver Disease Involving the Potent Suppression of Elevated Hepatic SCD-1.
Hepatic lipid partitioning and liver damage in nonalcoholic fatty liver disease: role of stearoyl-CoA desaturase.
In a pilot study, reduced fatty acid desaturase 1 function was associated with nonalcoholic fatty liver disease and response to treatment in children.
Isolation and Anti-Fatty Liver Activity of a Novel Cerebroside from the Sea Cucumber Acaudina molpadioides.
miR-192-5p regulates lipid synthesis in non-alcoholic fatty liver disease through SCD-1.
n-3 Polyunsaturated fatty acids for the management of alcoholic liver disease: A critical review.
N-glycosylation of CREBH improves lipid metabolism and attenuates lipotoxicity in NAFLD by modulating PPAR? and SCD-1.
Novel Lipid Long Intervening Noncoding RNA, Oligodendrocyte Maturation-Associated Long Intergenic Noncoding RNA, Regulates the Liver Steatosis Gene Stearoyl-Coenzyme A Desaturase As an Enhancer RNA.
Osthol attenuates hepatic steatosis via decreased triglyceride synthesis not by insulin resistance.
Stearoyl-CoA desaturase and tumorigenesis.
Stearoyl-CoA desaturase, a short-lived protein of endoplasmic reticulum with multiple control mechanisms.
Subtle metabolic and liver gene transcriptional changes underlie diet-induced fatty liver susceptibility in insulin-resistant mice.
TXNIP/VDUP1 attenuates steatohepatitis via autophagy and fatty acid oxidation.
Western diet-induced hepatic steatosis and alterations in the liver transcriptome in adult Brown-Norway rats.
[Effect of sea cucumber cerebroside on lipid metabolism in fatty liver rats.]
[Effects of soothing liver and invigorating spleen recipes on SREBP-1c, SCD-1 mRNA and proteins expression in hepatocytes of NAFLD rats].
[Research progress of stearoyl-CoA desaturase-1 on obesity and non-alcoholic fatty liver disease Abstract].
Obesity
A novel inhibitor of stearoyl-CoA desaturase-1 attenuates hepatic lipid accumulation, liver injury and inflammation in model of nonalcoholic steatohepatitis.
Adipose tissue palmitoleic acid and obesity in humans: does it behave as a lipokine?
Adipose tissue stearoyl-CoA desaturase mRNA is increased by obesity and decreased by polyunsaturated fatty acids.
Adipose-specific deletion of stearoyl-CoA desaturase 1 up-regulates the glucose transporter GLUT1 in adipose tissue.
Anthropometric indices and the risk of incident sudden cardiac death among adults with and without diabetes: over 15 years of follow-up in The Tehran Lipid and Glucose Study.
Association between increased visceral fat area and alterations in plasma fatty acid profile in overweight subjects: a cross-sectional study.
Associations between Chewing Difficulty, Subjective Cognitive Decline, and Related Functional Difficulties among Older People without Dementia: Focus on Body Mass Index.
Associations between estimated fatty acid desaturase activities in serum lipids and adipose tissue in humans: links to obesity and insulin resistance.
Associations between plasma polyunsaturated fatty acids, plasma stearoyl-CoA desaturase indices and body fat.
Associations of maternal and fetal SCD-1 markers with infant anthropometry and maternal diet: Findings from the ROLO study.
beta-Adrenergic control of stearoyl-CoA desaturase 1 repression in relation to sympathoadrenal regulation of thermogenesis.
Biochemical and Physiological Function of Stearoyl-CoA Desaturase.
Body composition in women with sickle cell disease.
Body Mass Index and Sudden Cardiac Death in Japanese Patients After Acute Myocardial Infarction: Data From the JCAD Study and HIJAMI-II Registry.
Body Mass Index and the Association With Vaso-occlusive Crises in Pediatric Sickle Cell Disease.
Cardiorenal Risk Prevalence in Sickle Cell Hemoglobinopathy.
Cardiorespiratory Fitness and Risk of Sudden Cardiac Death in Men and Women in the United States: A Prospective Evaluation From the Aerobics Center Longitudinal Study.
Causes of nonischemic sudden cardiac death in the current era.
Characterization of Gastric Electrical Activity Using Magnetic Field Measurements: A Simulation Study.
Characterization of HSCD5, a novel human stearoyl-CoA desaturase unique to primates.
Chronic administration of recombinant IL-6 upregulates lipogenic enzyme expression and aggravates high-fat-diet-induced steatosis in IL-6-deficient mice.
Citrus flavonoids repress the mRNA for stearoyl-CoA desaturase, a key enzyme in lipid synthesis and obesity control, in rat primary hepatocytes.
Despite antiatherogenic metabolic characteristics, SCD1-deficient mice have increased inflammation and atherosclerosis.
Diet-induced changes in stearoyl-CoA desaturase 1 expression in obesity-prone and -resistant mice.
Discovery and pharmacological characterization of SAR707 as novel and selective small molecule inhibitor of stearoyl-CoA desaturase (SCD1).
Discovery of Novel and Potent Stearoyl Coenzyme A Desaturase 1 (SCD1) Inhibitors as Anticancer Agents.
Discovery of piperazin-1-ylpyridazine-based potent and selective stearoyl-CoA desaturase-1 inhibitors for the treatment of obesity and metabolic syndrome.
Discovery of potent and liver-selective stearoyl-CoA desaturase (SCD) inhibitors in an acyclic linker series.
Discovery of potent and liver-targeted stearoyl-CoA desaturase (SCD) inhibitors in a bispyrrolidine series.
Discovery of potent liver-selective stearoyl-CoA desaturase-1 (SCD1) inhibitors, thiazole-4-acetic acid derivatives, for the treatment of diabetes, hepatic steatosis, and obesity.
Effects of DHEA on metabolic and endocrine functions of adipose tissue.
Erratum to: Stearoyl CoA desaturase 1 is elevated in obesity but protects against fatty acid-induced skeletal muscle insulin resistance in vitro.
Exercise Training Alters Red Blood Cell Fatty Acid Desaturase Indices and Adipose Tissue Fatty Acid Profile in African Women with Obesity.
Fatty Acid Bile Acid Conjugate Inhibits Hepatic Stearoyl Coenzyme A Desaturase and Is Non-atherogenic.
Fatty acid composition and estimated desaturase activities are associated with obesity and lifestyle variables in men and women.
Fatty acid composition of serum lipids predicts the development of the metabolic syndrome in men.
Fatty acid desaturation index in human plasma: comparison of different analytical methodologies for the evaluation of diet effects.
Genetic contributions to the expression of acquired causes of cardiac hypertrophy in non-ischemic sudden cardiac death victims.
Global deletion of lipocalin 2 does not reverse high-fat diet-induced obesity resistance in stearoyl-CoA desaturase-1 skin-specific knockout mice.
Growth status in children and adolescents with sickle cell disease.
Hexadecenoic Fatty Acid Isomers in Human Blood Lipids and Their Relevance for the Interpretation of Lipidomic Profiles.
High oleic/stearic fatty-acid desaturation index in cord plasma from infants of mothers with gestational diabetes.
High-Throughput Scintillation Proximity Assay for Stearoyl-CoA Desaturase-1.
Indices of fatty acid desaturase activity in healthy human subjects: effects of different types of dietary fat.
Inferolateral early repolarization among non-ischaemic sudden cardiac death victims.
Inhibition of stearoyl CoA desaturase activity induces hypercholesterolemia in the cholesterol-fed hamster.
Inhibition of stearoyl-CoA desaturase1 activates AMPK and exhibits beneficial lipid metabolic effects in vitro.
Inhibition of stearoyl-coenzyme A desaturase 1 dissociates insulin resistance and obesity from atherosclerosis.
Insights into Stearoyl-CoA Desaturase-1 Regulation of Systemic Metabolism.
Interleukin-6 derived from cutaneous deficiency of stearoyl-CoA desaturase- 1 may mediate metabolic organ crosstalk among skin, adipose tissue and liver.
Jacaric Acid, a Linolenic Acid Isomer with a Conjugated Triene System, Reduces Stearoyl-CoA Desaturase Expression in Liver of Mice.
Leptin and the control of metabolism: role for stearoyl-CoA desaturase-1 (SCD-1).
Leptin suppresses stearoyl-CoA desaturase 1 by mechanisms independent of insulin and sterol regulatory element-binding protein-1c.
Lipidomics Reveals a Link between CYP1B1 and SCD1 in Promoting Obesity.
Loss of stearoyl-CoA desaturase-1 improves insulin sensitivity in lean mice but worsens diabetes in leptin-deficient obese mice.
Meta-analysis approach identifies candidate genes and associated molecular networks for type-2 diabetes mellitus.
Metabolic syndrome and the risk of sudden cardiac death in middle-aged men.
Methylation levels of the SCD1 gene promoter and LINE-1 repeat region are associated with weight change: an intervention study.
Monounsaturated fatty acids generated via stearoyl CoA desaturase-1 are endogenous inhibitors of fatty acid amide hydrolase.
Novel substituted heteroaromatic compounds as inhibitors of stearoyl-CoA desaturase.
Nutrition-/diet-induced changes in gene expression in white adipose tissue.
Obesity - a perspective based on the biochemical interrelationship of lipids and carbohydrates.
Obesity and diabetes mellitus in patients with sickle cell disease.
Obesity resistance of the stearoyl-CoA desaturase-deficient (scd1-/-) mouse results from disruption of the epidermal lipid barrier and adaptive thermoregulation.
One-night sleep deprivation induces changes in the DNA methylation and serum activity indices of stearoyl-CoA desaturase in young healthy men.
Ontogeny of hepatic energy metabolism genes in mice as revealed by RNA-sequencing.
Out of hospital sudden cardiac death in Italy: a population-based case-control study.
Plasma stearoyl-CoA desaturase activity indices and bile acid concentrations after a low-fat meal: association with a genetic variant in the FTO gene.
Platyphylloside Isolated From Betula platyphylla Inhibit Adipocyte Differentiation and Induce Lipolysis Via Regulating Adipokines Including PPAR? in 3T3-L1 Cells.
Polymorphisms in stearoyl coa desaturase and sterol regulatory element binding protein interact with N-3 polyunsaturated fatty acid intake to modify associations with anthropometric variables and metabolic phenotypes in Yup'ik people.
Polymorphisms in the SCD1 gene are associated with indices of stearoyl CoA desaturase activity and obesity: A prospective study.
Polymorphisms in the SCD1 gene: associations with body fat distribution and insulin sensitivity.
Polymorphisms in the stearoyl-CoA desaturase gene modify blood glucose response to dietary oils varying in MUFA content in adults with obesity.
Postprandial effects of a meal low in sulfur amino acids and high in polyunsaturated fatty acids compared to a meal high in sulfur amino acids and saturated fatty acids on stearoyl CoA-desaturase indices and plasma sulfur amino acids: a pilot study.
Prevention of obesity in mice by antisense oligonucleotide inhibitors of stearoyl-CoA desaturase-1.
Recent Advances in Stearoyl-CoA Desaturase 1 Inhibitors for Dyslipidemia and Obesity.
Recent advances on stearoyl-CoA desaturase regulation in fatty liver diseases.
Regulation of stearoyl-CoA desaturase expression.
Relation of Body Mass Index Categories with Risk of Sudden Cardiac Death.
Role of stearoyl-coenzyme A desaturase in regulating lipid metabolism.
SAR and optimization of thiazole analogs as potent stearoyl-CoA desaturase inhibitors.
Serum fatty acid composition and indices of stearoyl-CoA desaturase activity are associated with systemic inflammation : longitudinal analyses in middle-aged men.
Serum fatty acid composition and insulin resistance are independently associated with liver fat markers in elderly men.
Skeletal Muscle Characteristics of Rats with Obesity, Diabetes, Hypertension, and Hyperlipidemia.
Skin-specific deletion of stearoyl-CoA desaturase-1 alters skin lipid composition and protects mice from high-fat diet-induced obesity.
Stearic acid content of abdominal adipose tissues in obese women.
Stearoyl CoA desaturase 1 is elevated in obesity but protects against fatty acid-induced skeletal muscle insulin resistance in vitro.
Stearoyl-CoA Desaturase 1 Is a Key Determinant of Membrane Lipid Composition in 3T3-L1 Adipocytes.
Stearoyl-CoA desaturase and its relation to high-carbohydrate diets and obesity.
Stearoyl-CoA desaturase as a new drug target for obesity treatment.
Stearoyl-CoA desaturase enzyme 1 inhibition reduces glucose utilization for de novo fatty acid synthesis and cell proliferation in 3T3-L1 adipocytes.
Stearoyl-CoA desaturase, a short-lived protein of endoplasmic reticulum with multiple control mechanisms.
Stearoyl-CoA desaturase-1 and the metabolic syndrome.
Stearoyl-CoA desaturase-1 deficiency attenuates obesity and insulin resistance in leptin-resistant obese mice.
Stearoyl-CoA Desaturase-1 Is Associated with Insulin Resistance in Morbidly Obese Subjects.
Stearoyl-CoA Desaturase: A Vital Checkpoint in the Development and Progression of Obesity.
Stearoyl-coenzyme A desaturase 1 gene expression increases after pioglitazone treatment and is associated with peroxisomal proliferator-activated receptor-gamma responsiveness.
Stearoylethanolamide exerts anorexic effects in mice via down-regulation of liver stearoyl-coenzyme A desaturase-1 mRNA expression.
Sterculic Oil, a natural inhibitor of SCD1, improves the metabolic state of obese OLETF rats.
Sterculic Oil, a Natural SCD1 Inhibitor, Improves Glucose Tolerance in Obese ob/ob Mice.
Sudden Cardiac Death Among Firefighters ?45 Years of Age in the United States.
Sudden Cardiac Death in the Young: Incidence, Trends, and Risk Factors in a Nationwide Study.
Sudden death in schizophrenia.
The fate and intermediary metabolism of stearic acid.
The role of stearoyl-CoA desaturase in body weight regulation.
The role of stearoyl-CoA desaturase in obesity, insulin resistance, and inflammation.
Transcript profiling suggests that differential metabolic adaptation of mice to a high fat diet is associated with changes in liver to muscle lipid fluxes.
Type I iodothyronine 5'-deiodinase mRNA and activity is increased in adipose tissue of obese subjects.
Vitamin A regulates obesity in WNIN/Ob obese rat; independent of stearoyl-CoA desaturase-1.
Weight status and health behaviors of adolescents and young adults with sickle cell disease: The emerging risk for obesity.
[An investigation of sudden cardiac death in apparently healthy young men by annual health examination.]
[Research progress of stearoyl-CoA desaturase-1 on obesity and non-alcoholic fatty liver disease Abstract].
Obesity, Abdominal
Abdominal adiposity is associated with fatty acid desaturase activity in boys: Implications for C-reactive protein and insulin resistance.
Association of Waist-Hip Ratio to Sudden Cardiac Death and Severe Coronary Atherosclerosis in Medicolegal Autopsies.
Obesity, Morbid
Impact of Bariatric Surgery on Outcomes of Patients with Sickle Cell Disease: a Nationwide Inpatient Sample Analysis, 2004-2014.
Rosiglitazone Requires Hepatocyte PPAR? Expression to Promote Steatosis in Male Mice With Diet-Induced Obesity.
Weight Loss as an Effective Strategy to Decrease Opioid Use and Frequency of Vaso-Occlusive Crises in Patients with Sickle Cell Disease.
Obstetric Labor, Premature
Opioid-Related Disorders Among Pregnant Women with Sickle Cell Disease and Adverse Pregnancy Outcomes.
Outcome of pregnancies complicated by sickle cell and sickle-C hemoglobinopathies.
Perinatal implications of sickle cell disease.
Sickle Cell Disease and Pregnancy.
Oligohydramnios
Third-trimester erythrocytapheresis in pregnant patients with sickle cell disease.
Oligospermia
Molecular evidence of apoptotic pathway activation in semen samples with high DNA fragmentation.
Seminal parameters of ejaculates collected from oligospermic and normospermic patients via masturbation and at intercourse with the use of a Silastic seminal fluid collection device.
The Effects of Treatment with Blood Transfusion, Iron Chelation and Hydroxyurea on Puberty, Growth and Spermatogenesis in Sickle Cell Disease (SCD): A short update.
Olivopontocerebellar Atrophies
Diffusion- and T2-weighted MRI of the transverse pontine fibres in spinocerebellar degeneration.
[A refined evaluation of cerebellar ataxia and its application to treatment of spinocerebellar degeneration]
[Brain stem auditory evoked potentials in spinocerebellar degeneration]
[Cerebello-cerebral functional relationship in spinocerebellar degeneration using positron emission tomography]
[Correlation of clinical course with MRI findings in olivo-pontocerebellar atrophy and late-cortical cerebellar atrophy]
[Efficacy of TRH-T for spinocerebellar degeneration--the relation between clinical features and effect of TRH therapy]
[Spinocerebellar degeneration in Japan--the feature from an epidemiological study]
[Study of the blink reflex in spinocerebellar degeneration]
Optic Atrophy
Optic disc edema associated with spinocerebellar degeneration.
Orbital Cellulitis
Frontal Bone Infarctions Masquerading as Bilateral Orbital Cellulitis in a Patient with Sickle Cell Disease.
Osteoarthritis
Long term prognosis of Scheuermann's disease: The association with fragility fracture - The MINOS cohort.
Total Hip Arthroplasty in Patients With Sickle Cell Disease: A Comprehensive Systematic Review.
Ultrasonographic Assessment of the Distal Femoral Cartilage Thickness in Patients with Homozygous Sickle Cell Disease.
Unusual sites of Salmonella osteoarthritis in patients with sickle cell disease: two cases.
Osteoarthritis, Hip
Preliminary Results of Multiple Epiphyseal Drilling and Autologous Bone Marrow Implantation for Osteonecrosis of the Femoral Head Secondary to Sickle Cell Disease in Children.
Osteomyelitis
A prospective study of soft-tissue ultrasonography in sickle cell disease patients with suspected osteomyelitis.
Bilateral mandibular osteomyelitis mimicking periapical cysts in a patient with sickle cell anemia.
Ceftriaxone-resistant Salmonella septicemia and osteomyelitis in sickle cell disease adults.
Contribution of Reduced Interleukin-10 Levels to the Pathogenesis of Osteomyelitis in Children with Sickle Cell Disease.
Detection of acute osteomyelitis with indium-111 labeled white blood cells in a patient with sickle cell disease.
Dilemma in differentiating between acute osteomyelitis and bone infarction in children with sickle cell disease: the role of ultrasound.
Emergence of ciprofloxacin resistance during treatment of Salmonella osteomyelitis in three patients with sickle cell disease.
Management of Osteomyelitis in Sickle Cell Disease: Review Article.
Microbiology and radiographic features of osteomyelitis in children and adolescents with sickle cell disease.
Multimodality Treatment for Nonhealing Wound With Osteomyelitis in Sickle Cell Disease.
Multiple bone and joint diseases in a nigerian sickle cell anaemia: a case report.
OCCURRENCE OF UNUSUAL HAEMOGLOBINOPATHIES IN BALOCHISTAN: HB SD AND HB SE - PRESENTATION WITH OSTEOMYELITIS.
Orofacial Manifestations in Patients with Sickle Cell Disease.
Orthopaedic Manifestations of Sickle Cell Disease.
Osteomyelitis in sickle cell haemoglobinopathy with elevated fetal haemoglobin.
Review of Sickle Cell Disease and Spinal Pathology.
Salmonella as a causative organism of various infections in patients with sickle cell disease.
Septic arthritis in adults with sickle cell disease often is associated with osteomyelitis or osteonecrosis.
Sickle cell disease promotes sex-dependent pathological bone loss through enhanced cathepsin proteolytic activity.
The diagnostic role of gadolinium enhanced MRI in distinguishing between acute medullary bone infarct and osteomyelitis.
Utility of unenhanced fat-suppressed T1-weighted MRI in children with sickle cell disease -- can it differentiate bone infarcts from acute osteomyelitis?
Osteonecrosis
Aseptic osteonecrosis of the femoral head in patients with sickle cell anemia.
Complete resolution of sickle cell chronic pain with high dose vitamin D therapy: a case report and review of the literature.
Core decompression and arthroplasty outcomes for atraumatic osteonecrosis of the humeral head.
Does Transcranial Direct Current Stimulation Combined with Peripheral Electrical Stimulation Have an Additive Effect in the Control of Hip Joint Osteonecrosis Pain Associated with Sickle Cell Disease? A Protocol for a One-Session Double Blind, Block-Randomized Clinical Trial.
Genomic polymorphisms in sickle cell disease: implications for clinical diversity and treatment.
Management of Osteomyelitis in Sickle Cell Disease: Review Article.
Managing femoral head osteonecrosis in patients with sickle cell disease.
Microfluidics in Sickle Cell Disease Research: State of the Art and a Perspective Beyond the Flow Problem.
Orthopaedic Manifestations of Sickle Cell Disease.
Osteonecrosis in sickle cell disease patients from Bahia, Brazil: a cross-sectional study.
Osteonecrosis of the femoral head in sickle cell disease: prevalence, comorbidities, and surgical outcomes in California.
Polymorphisms in Inflammatory Genes Modulate Clinical Complications in Patients With Sickle Cell Disease.
Quantification and Comprehensive Analysis of Mesenchymal Stromal Cells in Bone Marrow Samples from Sickle Cell Disease Patients with Osteonecrosis.
Septic arthritis in adults with sickle cell disease often is associated with osteomyelitis or osteonecrosis.
Sickle cell disease as a vascular disorder.
Sickle cell disease promotes sex-dependent pathological bone loss through enhanced cathepsin proteolytic activity.
Sickle cell disease subphenotypes in patients from southwestern province of saudi arabia.
Total Hip Arthroplasty in Patients With Sickle Cell Disease: A Comprehensive Systematic Review.
Treatment for avascular necrosis of bone in people with sickle cell disease.
[Diagnosis and surgical management of femoral head osteonecrosis in sickle cell disease]
Osteoporosis
Complete resolution of sickle cell chronic pain with high dose vitamin D therapy: a case report and review of the literature.
Cystathionine ?-synthase-deficient mice thrive on a low-methionine diet.
High prevalence and correlates of low bone mineral density in young adults with sickle cell disease.
Let-7c regulates proliferation and osteodifferentiation of human adipose-derived mesenchymal stem cells under oxidative stress by targeting SCD-1.
Long Term Ovariectomy-Induced Osteoporosis is Associated with High Stearoyl-CoA Desaturase Indexes in Rat Femur.
Microfluidics in Sickle Cell Disease Research: State of the Art and a Perspective Beyond the Flow Problem.
miRNA-429 suppresses osteogenic differentiation of human adipose-derived mesenchymal stem cells under oxidative stress via targeting SCD-1.
Predictors of abnormal bone mass density in adult patients with homozygous sickle-cell disease.
Review of Sickle Cell Disease and Spinal Pathology.
Secondary osteoporosis due to sickle cell anemia: Do sex steroids play a role?
Sickle cell disease promotes sex-dependent pathological bone loss through enhanced cathepsin proteolytic activity.
Osteosarcoma
Coffee intake mitigated inflammation and obesity-induced insulin resistance in skeletal muscle of high-fat diet-induced obese mice.
Combined bezafibrate, medroxyprogesterone acetate and valproic acid treatment inhibits osteosarcoma cell growth without adversely affecting normal mesenchymal stem cells.
DNA Microarray Analysis of the Mouse Adrenal Gland for the Detection of Hypothermia Biomarkers: Potential Usefulness for Forensic Investigation.
Stearoyl-CoA Desaturase-1 Attenuates the High Shear Force Damage Effect on Human MG63 Osteosarcoma Cells.
Otitis
hearing loss in Angolan children with sickle-cell disease.
Otitis Media
hearing loss in Angolan children with sickle-cell disease.
Otitis Media, Suppurative
Otological burdens of Nigerian children with sickle cell disease.
Otosclerosis
A Case Series of Patients With Concurrent Otosclerosis and Superior Semicircular Canal Dehiscence.
Otological burdens of Nigerian children with sickle cell disease.
Ototoxicity
Ototoxicity in hemoglobinopathy patients chelated with desferrioxamine.
Out-of-Hospital Cardiac Arrest
Prediction and prevention of sudden cardiac death.
Prognostic value of electrocardiographic time intervals and QT rate dependence in hypertrophic cardiomyopathy.
Prospective Countywide Surveillance and Autopsy Characterization of Sudden Cardiac Death: POST SCD Study.
Sudden Cardiac Death in the Young: A Strategy for Prevention by Targeted Evaluation.
Sudden death in ischemic heart disease - 2017.
[Sudden cardiac death: epidemiology and modern therapy]
Ovarian Neoplasms
Efficient iron utilization compensates for loss of extracellular matrix of ovarian cancer spheroids.
Ovarian Cancer-Why Lipids Matter.
Stearoyl CoA Desaturase Regulates Ferroptosis in Ovarian Cancer Offering New Therapeutic Perspectives.
Overweight
Associations between Chewing Difficulty, Subjective Cognitive Decline, and Related Functional Difficulties among Older People without Dementia: Focus on Body Mass Index.
Body Mass Index and the Association With Vaso-occlusive Crises in Pediatric Sickle Cell Disease.
Body Mass Index as a Predictor of Sudden Cardiac Death and Usefulness of the Electrocardiogram for Risk Stratification.
Cardiorespiratory Fitness and Risk of Sudden Cardiac Death in Men and Women in the United States: A Prospective Evaluation From the Aerobics Center Longitudinal Study.
Effects of two-months balanced diet in metabolically healthy obesity: lipid correlations with gender and BMI-related differences.
Genetic polymorphism of APOB is associated with diabetes mellitus in sickle cell disease.
Moderate chronic pain, weight and dietary intake in African-American adult patients with sickle cell disease.
Relation of Body Mass Index Categories with Risk of Sudden Cardiac Death.
Sudden cardiac death among Iranian population: a two decades follow-up of Tehran lipid and glucose study.
Weight status and health behaviors of adolescents and young adults with sickle cell disease: The emerging risk for obesity.
Weight Status of Children With Sickle Cell Disease.
Pancreatic Diseases
comparative study of carbohydrate antigen 19-9 in sickle cell disease subjects and controls in Nnamdi Azikiwe University Teaching Hospital, Nnewi, Nigeria.
Pancreatic Neoplasms
Effect of PPAR? Agonist on Stearoyl-CoA Desaturase 1 in Human Pancreatic Cancer Cells: Role of MEK/ERK1/2 Pathway.
Inhibition of Stearoyl-CoA Desaturase Induces the Unfolded Protein Response in Pancreatic Tumors and Suppresses Their Growth.
Stearoyl-CoA Desaturase 1 Potentiates Hypoxic plus Nutrient-Deprived Pancreatic Cancer Cell Ferroptosis Resistance.
Sterol regulatory element-binding protein 1 inhibitors decrease pancreatic cancer cell viability and proliferation.
Pancreatitis
Multiple primary choledocholithiasis in sickle cell disease.
Pancreatitis, Chronic
Survey of Physician Perspective towards Management of Pain for Chronic Conditions in the Emergency Department.
Papilledema
Optic disc edema associated with spinocerebellar degeneration.
Papillomavirus Infections
Prevalence and Factors Associated with Human Parvovirus B19 Infection in Sickle Cell Patients Hospitalized in Tanzania.
Paralysis
Spinocerebellar degeneration: Discrepancies between clinical and pathological diagnoses.
Subacute combined degeneration induced by nitrous oxide inhalation: Two case reports.
[Study on argyrophilic inclusions of multisystem atrophy (Oppenheimer)]
Paraparesis, Spastic
Chronic progressive spinocerebellar syndrome associated with antibodies to human T-lymphotropic virus type I: clinico-virological and magnetic resonance imaging studies.
Paraparesis, Tropical Spastic
Chronic progressive spinocerebellar syndrome associated with antibodies to human T-lymphotropic virus type I: clinico-virological and magnetic resonance imaging studies.
Paraproteinemias
Differential diagnosis of Schnyder corneal dystrophy.
Parasitemia
Malaria as a cause of morbidity and mortality in children with homozygous sickle cell disease on the coast of Kenya.
Robust adaptive immune response against Babesia microti infection marked by low parasitemia in a murine model of sickle cell disease.
Safety and effectiveness of antimalarial therapy in sickle cell disease: a systematic review and network meta-analysis.
Parasomnias
Sleep patterns in pediatric sickle cell disease.
Parathyroid Neoplasms
Primary Hyperparathyroidism in Sickle Cell Disease: An Unknown Complication of the Disease in Adulthood.
Paresis
Arteriopathy Influences Pediatric Ischemic Stroke Presentation, but Sickle Cell Disease Influences Stroke Management.
Paresthesia
A Case of Subacute Combined Degeneration of the Spinal Cord with Infective Endocarditis.
Parkinson Disease
A Novel Golgi Retention Signal RPWS for Tumor Suppressor UBIAD1.
Cognitive and cortical thinning patterns of subjective cognitive decline in patients with and without Parkinson's disease.
Finger tapping test as a means to differentiate olivo-ponto-cerebellar atrophy among spinocerebellar degenerations.
Novel therapeutic approaches for Parkinson's disease by targeting brain cholesterol homeostasis.
Quantitative evaluation of gait ataxia by accelerometers.
SCD Inhibition Protects from ?-Synuclein-Induced Neurotoxicity But Is Toxic to Early Neuron Cultures.
Stepping analysis in patients with spinocerebellar degeneration and Parkinson's disease.
Subjective cognitive decline predicts future deterioration in cognitively normal patients with Parkinson's disease.
Parvoviridae Infections
Simultaneous acute splenic sequestration and transient aplastic crisis in children with sickle cell disease.
Pediatric Obesity
Associations of maternal and fetal SCD-1 markers with infant anthropometry and maternal diet: Findings from the ROLO study.
Peptic Ulcer
Abdominal pain in children with sickle cell disease.
Helicobacter pylori infection in sickle cell disease.
Pericardial Effusion
Cardiac dilatation index as an indicator of terminal central congestion evaluated using postmortem CT and forensic autopsy data.
Perinatal Death
Outcome of pregnancies among women with sickle cell disease.
Outcome of pregnancies complicated by sickle cell and sickle-C hemoglobinopathies.
Periodontal Diseases
Sickle cell disease does not predispose to caries or periodontal disease.
The association between dental and periodontal diseases and sickle cell disease. A pilot case-control study.
Periodontitis
Periodontitis and dental caries occur together.
Peripheral Arterial Disease
Incidence and Predictors of Sudden Cardiac Death After a Major Non-Fatal Cardiovascular Event.
Sudden Cardiac Death After Non-ST-Segment Elevation Acute Coronary Syndrome.
Sudden cardiac death after PCI and CABG in the bare-metal stent era: Incidence, prevalence, and predictors.
Peripheral Nervous System Diseases
Peripheral nerve pathology in sickle cell disease mice.
Peripheral nervous system involvement in patients with sickle cell disease.
[A family of spino-cerebellar degeneration with disturbance of ocular movement, choreoathetosis, amyotrophy and dementia--a consideration in clinical features]
Peripheral Vascular Diseases
Carotid artery duplex scanning in preoperative assessment for coronary artery revascularization: the association between peripheral vascular disease, carotid artery stenosis, and stroke.
Racial differences in sudden cardiac death among hypertensive patients during antihypertensive therapy: The LIFE study.
Periprosthetic Fractures
Total Hip Arthroplasty in Patients With Sickle Cell Disease: A Comprehensive Systematic Review.
Peritonitis
Peritonitis rates for CAPD patients using the SCD 210 (Inpersol sterile connecting device): a Canadian survey.
Pheochromocytoma
Prevention of ventricular fibrillation, acute myocardial infarction (myocardial necrosis), heart failure, and mortality by bretylium: is ischemic heart disease primarily adrenergic cardiovascular disease?
Pituitary ACTH Hypersecretion
Immunohistochemical analysis of 11-beta-hydroxysteroid dehydrogenase type 2 and glucocorticoid receptor in subclinical Cushing's disease due to pituitary macroadenoma.
Severe infection including disseminated herpes zoster triggered by subclinical Cushing's disease: a case report.
Pituitary Neoplasms
Clinical significance of screening for subclinical Cushing's disease in patients with pituitary tumors.
Multihormonal pituitary adenoma concomitant with Pit-1 and Tpit lineage cells causing acromegaly associated with subclinical Cushing's disease: a case report.
Pleural Effusion
Systemic lupus erythematosus in a child with sickle cell disease.
Pneumococcal Infections
American Academy of Pediatrics. Committee on Infectious Diseases. Technical report: prevention of pneumococcal infections, including the use of pneumococcal conjugate and polysaccharide vaccines and antibiotic prophylaxis.
Assessing the Immunogenic Response of a Single Center's Pneumococcal Vaccination Protocol in Sickle Cell Disease.
Ceftriaxone-induced drug reaction mimicking acute splenic sequestration crisis in a child with hemoglobin SC disease.
Evaluation of newborn sickle cell screening programme in England: 2010-2016.
Invasive Pneumococcal Disease in Patients With Sickle Cell Disease.
Poor Long-Term Efficacy of Prevnar-13 in Sickle Cell Disease Mice Is Associated with an Inability to Sustain Pneumococcal-Specific Antibody Titers.
Prophylactic antibiotics for preventing pneumococcal infection in children with sickle cell disease.
Provision of pneumococcal prophylaxis for publicly insured children with sickle cell disease.
PspA family typing and PCR-based DNA fingerprinting with BOX A1R primer of pneumococci from the blood of patients in the USA with and without sickle cell disease.
Quinupristin-dalfopristin nonsusceptibility in pneumococci from sickle cell disease patients.
Severe pneumococcal sepsis and meningitis in human immunodeficiency virus-infected adults with sickle cell disease.
Statins protect against fulminant pneumococcal infection and cytolysin toxicity in a mouse model of sickle cell disease.
Streptococcus pneumoniae sepsis and meningitis during the penicillin prophylaxis era in children with sickle cell disease.
Pneumonia
Age-Related Emergency Department Reliance in Patients with Sickle Cell Disease.
Amelioration of inflammation and tissue damage in sickle cell model mice by Nrf2 activation.
Antibiotic Use and Respiratory Pathogens in Adults With Sickle Cell Disease and Acute Chest Syndrome.
Association of Antibiotic Choice With Hospital Length of Stay and Risk Factors for Readmission in Patients With Sickle Cell Disease and Acute Chest Syndrome: An Observational Cohort Study.
Association of Guideline-Adherent Antibiotic Treatment With Readmission of Children With Sickle Cell Disease Hospitalized With Acute Chest Syndrome.
Comorbid obstructive sleep apnea and increased risk for sickle cell disease morbidity.
Comparison of pneumococcal vaccination response in children with sickle cell disease: HbSS and HbSC.
COVID-19 and the pulmonary complications of sickle cell disease.
COVID-19 in individuals with sickle cell disease/trait compared with other Black individuals.
Effects of experimental asthma on inflammation and lung mechanics in sickle cell mice.
Histopathology of experimentally induced asthma in a murine model of sickle cell disease.
House Dust Mite-Induced Allergic Lung Inflammation Is Not Exacerbated in Sickle Cell Disease Mice.
In vitro lymphocyte blastogenic responses and cytokine production in sickle cell disease patients with acute pneumonia.
Inhaled Steroids Reduce Pain and sVCAM Levels in Individuals with Sickle Cell Disease: A Triple-Blind, Randomized Trial.
Laparoscopic splenic procedures in children: experience in 231 children.
Morbidity associated with sickle cell disease in pregnancy.
Phospholipase A2 levels in acute chest syndrome of sickle cell disease.
Seizures risk factors in sickle cell disease. The cooperative study of sickle cell disease.
Sickle cell disease in pregnancy: maternal complications in a medicaid-enrolled population.
Sickle cell disease is associated with higher mortality among patients hospitalized with ischemic bowel disease.
Sickle cell disease related mortality in Brazil, 2000-2018.
Stereotactic Catheter Drainage Versus Conventional Craniotomy for Severe Spontaneous Intracerebral Hemorrhage in the Basal Ganglia.
Streptococcus pneumoniae and Its Virulence Factors H2O2 and Pneumolysin Are Potent Mediators of the Acute Chest Syndrome in Sickle Cell Disease.
Targeting iNKT cells for the treatment of sickle cell disease.
Venous thromboembolism in pregnant women with sickle cell disease: a retrospective database analysis.
Pneumoperitoneum
Laparoscopic cholecystectomy in sickle cell disease patients: does operating time matter?
Physiologic effects of pneumoperitoneum in adults with sickle cell disease undergoing laparoscopic cholecystectomy (a case control study).
Pneumothorax
Evaluation and Management of Sternoclavicular Dislocation in the Emergency Department.
Polymyositis
Juvenile polymyositis with unremitting pain and progressive loss of motor and bulbar function on a background of sickle cell disease.
Polyneuropathies
Are PrP(C)s involved in some human myelin diseases? Relating experimental studies to human pathology.
Polyuria
Nocturnal enuresis in sickle cell disease.
Sickle cell nephropathy: challenging the conventional wisdom.
Posterior Leukoencephalopathy Syndrome
Nonaneurysmal Subarachnoid Hemorrhage in Sickle Cell Disease: Description of a Case and a Review of the Literature.
Postpartum Hemorrhage
Sickle cell disease in pregnancy: maternal complications in a medicaid-enrolled population.
Pre-Eclampsia
Dimethyl acetals, an indirect marker of the endogenous antioxidant plasmalogen level, are reduced in blood lipids of Sudanese pre-eclamptic subjects whose background diet is high in carbohydrate.
Improvement of maternal and fetal outcomes in women with sickle cell disease treated with early prophylactic erythrocytapheresis.
Morbidity and pregnancy outcomes associated with sickle cell anemia among Saudi women.
Outcome of pregnancies complicated by sickle cell and sickle-C hemoglobinopathies.
Perinatal implications of sickle cell disease.
Pregnancy outcomes in women with sickle-cell disease in low and high income countries: a systematic review and meta-analysis.
Severe pre-eclampsia among pregnant women with sickle cell disease and HIV.
Sickle cell anemia/sickle cell disease and pregnancy outcomes among ethnic tribes in India: an integrative mini-review.
Sickle cell disease and pregnancy outcomes: population-based study on 8.8 million births.
Sickle Cell Disease and Pregnancy.
The emerging challenge of optimal blood pressure management and hypertensive syndromes in pregnant women with sickle cell disease: a review.
White blood cell count as a predictor of the severity of sickle cell disease during pregnancy.
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Metabolic adaptation of acute lymphoblastic leukemia to the central nervous system microenvironment is dependent on Stearoyl CoA desaturase.
Sickle cell anemia and hematological neoplasias.
Pregnancy Complications
Sickle cell disease and pregnancy in Bahrain.
Sickle cell disease in pregnancy: maternal complications in a medicaid-enrolled population.
Sickle cell disease: current activities, public health implications, and future directions.
The influence of infant and maternal sickle cell disease on birth outcome and neonatal course.
Pregnancy Complications, Infectious
Opioid-Related Disorders Among Pregnant Women with Sickle Cell Disease and Adverse Pregnancy Outcomes.
Pregnancy, High-Risk
Complications in pregnant women with sickle cell disease.
Premature Birth
Sickle cell disease in pregnancy: maternal complications in a medicaid-enrolled population.
The influence of infant and maternal sickle cell disease on birth outcome and neonatal course.
Pressure Ulcer
Multiple bone and joint diseases in a nigerian sickle cell anaemia: a case report.
Pressure ulcers: an unusual complication of indwelling urethral catheter.
Priapism
Adenosine Deaminase Enzyme Therapy Prevents and Reverses the Heightened Cavernosal Relaxation in Priapism.
Adenosine signaling in normal and sickle erythrocytes and beyond.
An evidence-based approach to the treatment of adults with sickle cell disease.
Arterial Stiffness Impairment in Sickle Cell Disease Associated with Chronic Vascular Complications: The Multinational African CADRE Study.
Beneficial effect of the nitric oxide donor compound 3-(1,3-dioxoisoindolin-2-yl)benzyl nitrate on dysregulated phosphodiesterase 5, NADPH oxidase and nitrosative stress in the sickle cell mouse penis: implication for priapism treatment.
Clinical and Genetic Predictors of Priapism in Sickle Cell Disease: Results from the Recipient Epidemiology and Donor Evaluation Study III Brazil Cohort Study.
Efficacy and Safety of Manual Partial Red Cell Exchange in the Management of Severe Complications of Sickle Cell Disease in a Developing Country.
Emergency Department Visits and Inpatient Admissions Associated with Priapism among Males with Sickle Cell Disease in the United States, 2006-2010.
Emergency Medicine Management of Sickle Cell Disease Complications: An Evidence-Based Update.
Etilefrine for the prevention of priapism in adult sickle cell disease.
Excess adenosine A2B receptor signaling contributes to priapism through HIF-1? mediated reduction of PDE5 gene expression.
Excess adenosine in murine penile erectile tissues contributes to priapism via A(2B) adenosine receptor signaling.
Genome-wide association study of erythrocyte density in sickle cell disease patients.
Genomic polymorphisms in sickle cell disease: implications for clinical diversity and treatment.
Haematological parameters associated with priapism in Nigerian patients with homozygous sickle cell disease.
Hemolysis-associated priapism in sickle cell disease.
Increased adenosine contributes to penile fibrosis, a dangerous feature of priapism, via A2B adenosine receptor signaling.
Increased cavernosal relaxations in sickle cell mice priapism are associated with alterations in the NO-cGMP signaling pathway.
Investigational agents for sickle cell disease.
Ischemic priapism in South-East Nigeria: Presentation, management challenges, and aftermath issues.
Laparoscopic splenic procedures in children: experience in 231 children.
Low nitric oxide level is implicated in sickle cell disease and its complications in Ghana.
Mechanisms of vasculopathy in sickle cell disease and thalassemia.
Mechanisms underlying priapism in sickle cell disease: targeting and key innovations on the preclinical landscape.
Medical management of ischemic stuttering priapism: a contemporary review of the literature.
Men with sickle cell disease experience greater sexual dysfunction when compared with men without sickle cell disease.
Molecular Analysis of Erection Regulatory Factors in Sickle Cell Disease-Associated Priapism in Human Penis.
Multisystem damage associated with tricorporal priapism in sickle cell disease.
Opiorphin is a master regulator of the hypoxic response in corporal smooth muscle cells.
Prevalence of Priapism and Its Awareness amongst Male Homozygous Sickle Cell Patients in Lagos, Nigeria.
Preventive treatment of priapism in sickle cell disease with oral and self-administered intracavernous injection of etilefrine.
Priapism and Sickle Cell Disease: Special Considerations in Etiology, Management, and Prevention.
Priapism and Sickle-Cell Anemia: Diagnosis and Nonsurgical Therapy.
Priapism complicating sickle cell disease in Nigerian children.
Priapism in Homozygous Sickle Cell Patients: Important Clinical and Laboratory Associations.
Priapism in Sickle Cell Disease: An Evaluation of the Knowledge of an at Risk Population in Jamaica.
Priapism in sickle cell disease: Associations between NOS3 and EDN1 genetic polymorphisms and laboratory biomarkers.
Priapism in Sickle-Cell Disease: A Hematologist's Perspective.
Resolution of Acute Priapism in Two Children With Sickle Cell Disease Who Received Nitrous Oxide.
Safety and efficacy of blood exchange transfusion for priapism complicating sickle cell disease.
Sexual Health Outcomes Improvement in Sickle Cell Disease: A Matter of Health Policy?
Sickle cell disease as a vascular disorder.
Sickle Cell Disease in Priapism: Disparity in Care?
Sickle cell disease subphenotypes in patients from southwestern province of saudi arabia.
Sickle cell leg ulcers: a frequently disabling complication and a marker of severity.
Subclinical Cardiac Dysfunction Is Associated With Extracardiac Organ Damages.
Testosterone induced priapism in two adolescents with sickle cell disease.
Testosterone replacement in transgenic sickle cell mice controls priapic activity and upregulates PDE5 expression and eNOS activity in the penis.
Testosterone replacement therapy does not promote priapism in hypogonadal men with sickle cell disease: 12-month safety report.
Testosterone Replacement Therapy in Adolescents With Sickle Cell Disease Reverses Hypogonadism Without Promoting Priapism: A Case Report.
The prevalence of priapism in children and adolescents with sickle cell disease in Brazil.
The Red Blood Cell-Inflammation Vicious Circle in Sickle Cell Disease.
Treatment of priapism in pediatric patients with sickle cell disease.
Trends in Sickle Cell Disease-related Priapism in U.S. Children's Hospitals.
Variations and characteristics of the various clinical phenotypes in a cohort of Nigerian sickle cell patients.
[Blood transfusion assessment to 112 homozygous sickle-cell disease patients in university hospital of Brazzaville.]
Primary Dysautonomias
Autonomic nervous system involvement in sickle cell disease.
Progressive vasoconstriction with sequential thermal stimulation indicates vascular dysautonomia in sickle cell disease.
Prostatic Neoplasms
Abrogation of de novo lipogenesis by stearoyl-CoA desaturase 1 inhibition interferes with oncogenic signaling and blocks prostate cancer progression in mice.
Inhibition of fatty acid desaturation is detrimental to cancer cell survival in metabolically compromised environments.
Inhibition of Stearoyl-CoA Desaturase by Sterculic Oil Reduces Proliferation and Induces Apoptosis in Prostate Cancer Cell Lines.
Stearoyl CoA desaturase (SCD) facilitates proliferation of prostate cancer cells through enhancement of androgen receptor transactivation.
protein acetyllysine n-acetyltransferase deficiency
Sirt1 counteracts decrease in membrane phospholipid unsaturation and diastolic dysfunction during saturated fatty acid overload.
Protein C Deficiency
Moyamoya syndrome as a risk factor for stroke in Saudi children. Novel and usual associations.
Protein S Deficiency
Thrombin generation and cell-dependent hypercoagulability in sickle cell disease.
Protein-Energy Malnutrition
Plasma fatty acid status in Moroccan children: increased lipid peroxidation and impaired polyunsaturated fatty acid metabolism in protein-calorie malnutrition.
Transport proteins and acute phase reactant proteins in children with sickle cell anemia.
Proteinuria
Abnormal Ambulatory Blood Pressure and Early Renal Dysfunction in Sickle Cell Disease.
All-Cause Mortality and Incidence of Major Adverse Cardiac Events in Sickle Cell Nephropathy: A Comparative Study.
An evidence-based approach to the treatment of adults with sickle cell disease.
Comparison of renal function markers in Kuwaiti patients with sickle cell disease.
Cystatin C, Beta2 Microglobulin, N-Acetyl-beta-D-glucosaminidase, Retinol-Binding Protein, and Endothelin 1 Levels in the Evaluation of Sickle Cell Disease Nephropathy.
Hemoglobin inhibits albumin uptake by proximal tubule cells: implications for sickle cell disease.
Interventions for chronic kidney disease in people with sickle cell disease.
Kidney Disease among Patients with Sickle Cell Disease, Hemoglobin SS and SC.
Kidney function, urinalysis abnormalities and correlates in equatorial Africans with sickle cell disease.
MYH9 and APOL1 are both associated with sickle cell disease nephropathy.
Prevalence and clinical correlates of glomerulopathy in children with sickle cell disease.
Progressive Decline in Estimated GFR in Patients With Sickle Cell Disease: An Observational Cohort Study.
Proteinuria in adult Saudi patients with sickle cell disease is not associated with identifiable risk factors.
Proteinuria in children with sickle cell disease.
Proteinuria in patients with sickle cell disease.
Proteinuria is associated with elevated tricuspid regurgitant jet velocity in children with sickle cell disease.
Renal abnormalities in patients with sickle cell disease: a single center report from saudi arabia.
Roles of APOL1 G1 and G2 variants in sickle cell disease patients: kidney is the main target.
Sickle Cell Disease and the Kidney: Pathophysiology and Novel Biomarkers.
[Spectrum of renal manifestations in sickle cell disease].
Pseudotumor Cerebri
Pseudotumor cerebri in children with sickle cell disease: a case series.
Psoriasis
Optimizing the frequency of outpatient short-contact dithranol treatment used in combination with broadband ultraviolet B for psoriasis: a randomized, within-patient controlled trial.
Psychomotor Agitation
The pain of children with sickle cell disease: the nursing approach.
Puberty, Delayed
Body composition in children with sickle cell disease.
Common gynecological challenges in adolescents with sickle cell disease.
Pulmonary Arterial Hypertension
Acute, Bilateral, Concurrent Central Retinal Artery Occlusion in Sickle Cell Disease After Use of Tadalafil (Cialis).
Hospitalization for pain in patients with sickle cell disease treated with sildenafil for elevated TRV and low exercise capacity.
Platelet activation in patients with sickle disease, hemolysis-associated pulmonary hypertension, and nitric oxide scavenging by cell-free hemoglobin.
Review: Hemodynamic Characteristics and Outcomes of Sickle Cell Disease Associated Pulmonary Hypertension.
Severe COVID-19 with acute respiratory distress syndrome (ARDS) in a sickle cell disease adult patient: case report.
The interaction between sickle cell disease and HIV infection: a systematic review.
Pulmonary Atresia
Spondylocostal dysostosis with tetralogy of Fallot and herniation of the spleen through the diaphragm.
Pulmonary Disease, Chronic Obstructive
An association between right ventricular dysfunction and sudden cardiac death.
Chronic Obstructive Pulmonary Disease and Risk of Sudden Cardiac Death.
Chronic obstructive pulmonary disease and sudden cardiac death: A systematic review.
Chronic obstructive pulmonary disease and sudden cardiac death: the Rotterdam study.
Reduced left ventricular ejection fraction and sudden cardiac death in patients undergoing revascularization: Time to remember the other players of the game.
Relation of Chronic Obstructive Pulmonary Disease to Cardiovascular Disease in the General Population.
Sudden cardiac death after acute heart failure hospital admission: insights from ASCEND-HF.
Sudden cardiac death after PCI and CABG in the bare-metal stent era: Incidence, prevalence, and predictors.
[Sudden Cardiac Death in Patients With Chronic Obstructive Pulmonary Disease].
Pulmonary Edema
Identification of Pulmonary Edema in Forensic Autopsy Cases of Sudden Cardiac Death Using Fourier Transform Infrared Microspectroscopy: A Pilot Study.
Spatiotemporal dysfunction of the vascular permeability barrier in transgenic mice with sickle cell disease.
Pulmonary Embolism
Arrhythmogenic right ventricular cardiomyopathy and sudden cardiac death in young Koreans.
Comparison of sequential compression devices and foot pumps for prophylaxis of deep venous thrombosis in high-risk trauma patients.
Fertility preservation before hematopoetic stem cell transplantation: a case series of women with GATA binding protein 2 deficiency, dedicator of cytokinesis 8 deficiency, and sickle cell disease.
In-hospital Outcomes and Characteristics of Heart Failure in Sickle Cell Disease.
Integrating Fat Embolism Syndrome Scoring Indices in Sickle Cell Disease: A Practice Management Review.
Pulmonary complications for women with sickle cell disease in pregnancy: systematic review and meta-analysis.
Pulmonary CTA in sickle cell patients: quantitative assessment of enhancement quality.
Sequential Pneumatic Compression in the Arm in Neurocritical Patients with a Peripherally Inserted Central Venous Catheter: A Randomized Trial.
Sickle cell disease in pregnancy: maternal complications in a medicaid-enrolled population.
Sickle cell disease, sickle trait and the risk for venous thromboembolism: a systematic review and meta-analysis.
The pattern of indications and complications of splenectomy in Eastern Saudi Arabia.
Venous thromboembolism incidence in the Cooperative Study of Sickle Cell Disease.
Venous Thromboembolism Prophylaxis in Orthopaedic Trauma Patients: A Survey of OTA Member Practice Patterns and OTA Expert Panel Recommendations.
Pulmonary Fibrosis
Circulating fibrocytes as biomarkers of impaired lung function in adults with sickle cell disease.
Pulmonary complications of hemoglobinopathies.
Pulmonary Heart Disease
Severe COVID-19 with acute respiratory distress syndrome (ARDS) in a sickle cell disease adult patient: case report.
Pulmonary Infarction
Large-vessel occlusion in sickle cell disease: pathogenesis, clinical consequences, and therapeutic implications.
Pulmonary Valve Insufficiency
Left ventricular dysfunction is a risk factor for sudden cardiac death in adults late after repair of tetralogy of Fallot.
Surgical ablation of ventricular tachycardia in patients with repaired tetralogy of Fallot.
Purpura, Thrombocytopenic, Idiopathic
Splenectomy for haematological disorders: A single center study in 150 patients from Oman.
Purpura, Thrombotic Thrombocytopenic
The rate of hemolysis in sickle cell disease correlates with the quantity of active von Willebrand factor in the plasma.
Pyelonephritis
Association of HIV infection with clinical and laboratory characteristics of sickle cell disease.
Morbidity associated with sickle cell disease in pregnancy.
[Arterial hypertension and sudden cardiac death]
Quadriplegia
A randomized blinded comparison of two methods used for venous antistasis in tetraplegia.
Red-Cell Aplasia, Pure
Assessment of liver and cardiac iron overload using MRI in patients with chronic anemias in Latin American countries: results from ASIMILA study.
Refractive Errors
Changes in the cornea related to sickle cell disease: a pilot investigation.
Height, weight, body mass index and ocular biometry in patients with sickle cell disease.
Ocular manifestations of sickle cell disease and genetic susceptibility for refractive errors.
Renal Insufficiency
Assessment of renal function in Indian patients with sickle cell disease.
Changes in urine albumin to creatinine ratio with the initiation of hydroxyurea therapy among children and adolescents with sickle cell disease.
Combination erythropoietin-hydroxyurea therapy in sickle cell disease: experience from the National Institutes of Health and a literature review.
Heart rate variability (HRV) in kidney failure: measurement and consequences of reduced HRV.
High one year mortality in adults with sickle cell disease and end-stage renal disease.
Investigations of Kidney Dysfunction-Related Gene Variants in Sickle Cell Disease Patients in Cameroon (Sub-Saharan Africa).
Prevalence and correlates of microalbuminuria in Yemeni children with sickle cell disease.
Prevalence of Microalbuminuria in Adult Patients with Sickle Cell Disease in Eastern Saudi Arabia.
Prevention of sudden cardiac death in patients with chronic kidney disease.
Proteinuria in adult Saudi patients with sickle cell disease is not associated with identifiable risk factors.
Renal abnormalities in patients with sickle cell disease: a single center report from saudi arabia.
Renal kallikrein: a risk marker for nephropathy in children with sickle cell disease.
Risk assessment for sudden cardiac death in dialysis patients: How relevant are conventional cardiac risk factors?
Risk factors for sudden cardiac death in patients with chronic renal insufficiency and left ventricular dysfunction.
Successful combined heart and kidney transplantation in a patient with sickle-cell anemia.
Technetium-99m-dimercaptosuccinic acid renal scintigraphy and single photon emission computed tomography/computed tomography in patients with sickle cell disease.
Renal Insufficiency, Chronic
All-Cause Mortality and Incidence of Major Adverse Cardiac Events in Sickle Cell Nephropathy: A Comparative Study.
Assessment of renal function in Indian patients with sickle cell disease.
Chronic kidney disease is common in sickle cell disease: a cross-sectional study in the Tema Metropolis, Ghana.
Cobalamin status in sickle cell disease.
Combined effect of renal function and serum potassium level in sudden cardiac death in aging hypertensive subjects.
Early and prominent alterations in hemodynamics, signaling, and gene expression following renal ischemia in sickle cell disease.
Endothelin in renal injury due to sickle cell disease.
Incidence and Predictors of Sudden Cardiac Death After a Major Non-Fatal Cardiovascular Event.
Increased expression of stearoyl-CoA desaturase (SCD1) in the adipose tissue contributes to serum content of monounsaturated fatty acids (MUFA) in patients with chronic kidney disease.
Interventions for chronic kidney disease in people with sickle cell disease.
Is renal medullary carcinoma the seventh nephropathy in sickle cell disease? A multi-center Nigerian survey.
Kidney biopsy findings in children with sickle cell disease: a Midwest Pediatric Nephrology Consortium study.
Predictors of renal function progression in adults with homozygous sickle cell disease.
Prevention of sudden cardiac death in patients with chronic kidney disease.
Reduction of stearoyl-CoA desaturase (SCD) contributes muscle atrophy through the excess endoplasmic reticulum stress in chronic kidney disease.
Risk factors for sudden cardiac death in patients with chronic renal insufficiency and left ventricular dysfunction.
Sickle cell disease and albuminuria: recent advances in our understanding of sickle cell nephropathy.
Sickle cell disease and the kidney.
Sickle Cell Disease and the Kidney: Pathophysiology and Novel Biomarkers.
Sudden cardiac death after PCI and CABG in the bare-metal stent era: Incidence, prevalence, and predictors.
The Economic Burden of End-Organ Damage Among Medicaid Patients with Sickle Cell Disease in the United States: A Population-Based Longitudinal Claims Study.
The kidney in sickle hemoglobinopathies?.
The prevalence of electrocardiographic early repolarization in an adult cohort with chronic kidney disease and its impact upon all-cause mortality and progression to dialysis.
Updating the lipids hypothesis of inflammation and vascular disease in patients with chronic kidney disease: a stearoyl-CoA desaturase affair?
Reperfusion Injury
Acute hydroxyurea treatment reduces tubular damage following bilateral ischemia-reperfusion injury in a mouse model of sickle cell disease.
Clinical biomarkers in sickle cell disease.
Coagulation abnormalities of sickle cell disease: Relationship with clinical outcomes and the effect of disease modifying therapies.
Fertility challenges for women with sickle cell disease.
Neuropathic pain in individuals with sickle cell disease.
Nrf2 activation in myeloid cells and endothelial cells differentially mitigates sickle cell disease pathology in mice.
Pathophysiology of Sickle Cell Disease.
Redox-dependent impairment of vascular function in sickle cell disease.
Sickle cell disease, vasculopathy, and therapeutics.
The glomerulopathy of sickle cell disease.
Respiratory Distress Syndrome
Integrating Fat Embolism Syndrome Scoring Indices in Sickle Cell Disease: A Practice Management Review.
Sickle cell disease in pregnancy: maternal complications in a medicaid-enrolled population.
Respiratory Hypersensitivity
Airway inflammation in sickle cell disease-A translational perspective.
Altered fatty acid metabolism and reduced stearoyl-coenzyme a desaturase activity in asthma.
Asthma and sickle cell disease: two distinct diseases or part of the same process?
Asthma in sickle cell disease.
Methacholine challenge in children with sickle cell disease: a case series.
Respiratory Insufficiency
Extracorporeal membrane oxygenation for the treatment of adult sickle cell acute chest syndrome.
In-hospital Outcomes and Characteristics of Heart Failure in Sickle Cell Disease.
Sickle cell disease is associated with higher mortality among patients hospitalized with ischemic bowel disease.
Sickle cell disease related mortality in Brazil, 2000-2018.
Spinal cord dysfunction after COVID-19 infection.
Spontaneous breathing during extracorporeal membrane oxygenation treatment of sickle cell disease acute chest syndrome.
The bivalent ligand MCC22 potently attenuates nociception in a murine model of sickle cell disease.
[Antidotal effects of sulfhydryl compounds on acute poisonings by sodium ammonium dimethyl-2-(propane-1,3-dithiosulfate) monohydrate, nereistoxin and cartap]
Respiratory Tract Infections
Molecular testing for respiratory pathogens in sickle cell disease adult patients presenting with febrile acute chest syndrome.
Sickle-cell disease in febrile children living in a rural village of Madagascar and association with malaria and respiratory infections.
Streptococcus pneumoniae and Its Virulence Factors H2O2 and Pneumolysin Are Potent Mediators of the Acute Chest Syndrome in Sickle Cell Disease.
Restless Legs Syndrome
Sequential compression devices for treatment of restless legs syndrome.
Retinal Artery Occlusion
Acute, Bilateral, Concurrent Central Retinal Artery Occlusion in Sickle Cell Disease After Use of Tadalafil (Cialis).
Recurrent orbital bone sub-periosteal hematoma in sickle cell disease: a case study.
Sudden-onset blindness in sickle cell disease due to retinal artery occlusion.
Retinal Detachment
When should children and young adults with sickle cell disease be referred for eye assessment?
Retinal Diseases
Fenretinide Induces Ubiquitin-Dependent Proteasomal Degradation of Stearoyl-CoA Desaturase in Human Retinal Pigment Epithelial Cells.
Genome-Wide Transcriptomic Analysis Identifies Pathways Regulated by Sterculic Acid in Retinal Pigmented Epithelium Cells.
Sterculic Acid: The Mechanisms of Action beyond Stearoyl-CoA Desaturase Inhibition and Therapeutic Opportunities in Human Diseases.
Retinal Neovascularization
Increased circulating PEDF and low sICAM-1 are associated with sickle cell retinopathy.
Reye Syndrome
Primary systemic carnitine deficiency presenting as recurrent Reye-like syndrome and dilated cardiomyopathy.
Rhabdomyolysis
Increased Rates of Rhabdomyolysis in Male Hematopoietic Cell Transplantation Recipients Taking Sirolimus and Trimethoprim/Sulfamethoxazole.
Kidney transplantation from donors with rhabdomyolysis and acute renal failure.
Recurrent aborted sudden cardiac death with seizures and rhabdomyolysis due to bulimia-induced hypokalemia: report of one case.
Rhabdomyoma
Benign cardiac tumours associated with sudden death.
Riboflavin Deficiency
Dependence of pyridoxine metabolism on riboflavin status in sickle cell patients.
Romano-Ward Syndrome
Detecting Underlying Cardiovascular Disease in Young Competitive Athletes.
Rubella
Immunologic effects of hydroxyurea in sickle cell anemia.
Salmonella Infections
Community-acquired Salmonella bacteraemia in patients with sickle-cell disease 1969-2008: A single centre study.
Salmonella as a causative organism of various infections in patients with sickle cell disease.
Salmonella bacteraemia in sickle cell disease at King's College Hospital: 1976-1991.
Severity of Salmonella infection among sickle cell diseases pediatric patients: Description of the infection pattern.
Sarcoidosis
Sudden cardiac death in nonischemic cardiomyopathy: Refining risk assessment.
[Antiarrhythmic agents in the prevention of sudden cardiac death]
[Sudden cardiac death in athletes: is it always not preventable?].
Sarcoma
Macrophage migration inhibitory factor and stearoyl-CoA desaturase 1: potential prognostic markers for soft tissue sarcomas based on bioinformatics analyses.
Squamous Cell Differentiation in Metastatic Papillary Thyroid Carcinoma: Metaplastic Reversion or Progression?
Sarcoma, Ewing
Identifying the molecular phenotype of renal progenitor cells.
[Expression of metanephric differentiation markers in human mesenchymal stem cells].
Schistosomiasis haematobia
Prevalence and factors associated with renal dysfunction among children with sickle cell disease attending the sickle cell disease clinic at a tertiary hospital in Northwestern Tanzania.
Scoliosis
Diffuse skull base/cervical fusion syndromes in two siblings with spondylocostal dysostosis syndrome: analysis via three dimensional computed tomography scanning.
Spondylocostal dysostosis with tetralogy of Fallot and herniation of the spleen through the diaphragm.
Tranexamic acid use in a patient with sickle cell disease undergoing posterior scoliosis correction surgery: safely mitigating bleeding and vaso-occlusive crises.
Seizures
Diagnostic and treatment difficulties in systemic lupus erythematosus coexisting with sickle cell disease.
Electroencephalography hyperventilation and stroke in children with sickle cell disease.
Encephaloduroarteriosynangiosis and encephalomyoarteriosynangiosis for treatment of moyamoya syndrome in pediatric patients with sickle cell disease.
Malaria in patients with sickle cell anaemia: burden, risk factors and outcome at the Laquintinie hospital, Cameroon.
Recent developments in the management of patients at risk for sudden cardiac death.
Recurrent aborted sudden cardiac death with seizures and rhabdomyolysis due to bulimia-induced hypokalemia: report of one case.
Risk factors for complications after abdominal surgery in children with sickle cell disease.
Seizures in the Jamaica cohort study of sickle cell disease.
Seizures risk factors in sickle cell disease. The cooperative study of sickle cell disease.
Significance of automated external defibrillator in identifying lethal ventricular arrhythmias.
The role of ion channelopathies in sudden cardiac death: implications for clinical practice.
Underestimation of sudden deaths among patients with seizures and epilepsy.
Unique clinical characteristics and SCN5A mutations in patients with Brugada syndrome in Taiwan.
[Antidotal effects of 2,3-dimercaptopropane-1-sulfonate sodium (DMPS) and combined with diazepam on acute poisoning caused by sodium ammonium dimethyl-2-propano-1,3-dithiosulfate monohydrate (SCD)]
Semicircular Canal Dehiscence
Cervical and Ocular VEMP Testing in Diagnosing Superior Semicircular Canal Dehiscence.
Longitudinal Cognitive and Neurobehavioral Functional Outcomes Before and After Repairing Otic Capsule Dehiscence.
Measurements of human middle- and inner-ear mechanics with dehiscence of the superior semicircular canal.
Surgical treatments for a case of superior canal dehiscence syndrome associated with patulous Eustachian tube.
The Sensitivity of the cVEMP Test in Detecting A Superior Semicircular Canal Dehiscence and the Influence of a Coexisting Incudal Lysis: A Case Report.
Sepsis
A biomimetic membrane device that modulates the excessive inflammatory response to sepsis.
Bloodstream infection in adults with sickle cell disease: association with venous catheters, Staphylococcus aureus, and bone-joint infections.
Care of the child with sickle cell disease: acute complications.
Ceftriaxone-resistant Salmonella septicemia and osteomyelitis in sickle cell disease adults.
Children with sickle cell disease and human immunodeficiency virus-1 infection: use of inpatient care services in the United States.
Epidemiology of Bloodstream Infections in Children with Sickle Cell Disease.
Hemopexin and haptoglobin: allies against heme toxicity from hemoglobin not contenders.
Improvement of maternal and fetal outcomes in women with sickle cell disease treated with early prophylactic erythrocytapheresis.
Increased intestinal permeability exacerbates sepsis through reduced hepatic SCD-1 activity and dysregulated iron recycling.
Invasive Pneumococcal Disease in Patients With Sickle Cell Disease.
Morbidity associated with sickle cell disease in pregnancy.
Mortality in sickle cell disease: A population-based study in an aboriginal community in the Gudalur Valley, Nilgiris, Tamil Nadu, India.
Penicillin- and cephalosporin-resistant strains of Streptococcus pneumoniae causing sepsis and meningitis in children with sickle cell disease.
Predictors of Bacteremia Among Children With Sickle Cell Disease Presenting With Fever.
Prevalence of Bartonella spp. Infection in Patients with Sickle Cell Disease.
Prophylaxis of pneumococcal infection in sickle-cell disease by the combined use of vaccination and penicillin.
Salmonella as a causative organism of various infections in patients with sickle cell disease.
Septic complications after splenectomy for sickle cell sequestration crisis.
Severe, non specific symptoms in non-typhoidal Salmonella infections in adult patients with sickle cell disease: a retrospective multicentre study.
Sickle cell disease in pregnancy: maternal complications in a medicaid-enrolled population.
Sickle cell disease related mortality in Brazil, 2000-2018.
Sickle cell disease: a neglected chronic disease of increasing global health importance.
The interaction between sickle cell disease and HIV infection: a systematic review.
The spleen in the sickling disorders: an update.
Total Hip Arthroplasty in Patients With Sickle Cell Disease: A Comprehensive Systematic Review.
Shock, Cardiogenic
In-hospital Outcomes and Characteristics of Heart Failure in Sickle Cell Disease.
The use of extracorporeal membrane oxygenation in pediatric patients with sickle cell disease.
Shy-Drager Syndrome
[Spinocerebellar degeneration in Japan--the feature from an epidemiological study]
Sick Sinus Syndrome
Clinical characterisation and long-term prognosis of women with Brugada syndrome.
Mechanism and prediction of sudden cardiac death in arrhythmia patients using electrophysiological studies.
Sickle Cell Trait
A simple, rapid, low-cost diagnostic test for sickle cell disease.
Acute appendicitis in patients with sickle cell disease.
Acute care utilization in pediatric sickle cell disease and sickle cell trait in the USA: prevalence, temporal trends, and cost.
Acute splenic sequestration crises in Saudi children with sickle cell disease.
Association of Inflammatory Biomarker C-Reactive Protein, Lipid Peroxidation and Antioxidant Capacity Marker with HbF Level in Sickle Cell Disease Patients from Chattisgarh.
Attitudes and impact among people with abnormal premarital screening test results in Muscat governorate's primary healthcare centers in 2018.
Birth Prevalence of Sickle Cell Trait and Sickle Cell Disease in Shelby County, TN.
Cellular function reinstitution of offspring red blood cells cloned from the sickle cell disease patient blood post CRISPR genome editing.
Characterization of Sickling During Controlled Automated Deoxygenation with Oxygen Gradient Ektacytometry.
Chronic Disease Management in Sickle Cell Trait Patients in the Primary Care Setting: A Case Report.
Clinical and laboratory features of sickle cell disease in The Netherlands.
Coexistence of lupus nephritis and sickle cell trait, an electron microscopic assessment of renal glomerular damage: Case report of a rare association.
Communication of positive newborn screening results for sickle cell disease and sickle cell trait: variation across states.
Distribution of haemoglobin genotypes, knowledge, attitude and practices towards sickle cell disease among unmarried youths in the Buea Health District, Cameroon.
Epidemiology and disease burden of sickle cell disease in France: A descriptive study based on a French nationwide claim database.
Etilefrine for the prevention of priapism in adult sickle cell disease.
Extremely high birth prevalence of sickle cell disease in rural Tanzania.
Factor V Leiden G1691A and prothrombin G20210A mutations among Palestinian patients with sickle cell disease.
Genetic variant in the BCL11A (rs1427407), but not HBS1-MYB (rs6934903) loci associate with fetal hemoglobin levels in Indian sickle cell disease patients.
Genetics of fetal hemoglobin in tribal Indian patients with sickle cell anemia.
Herbal Drug Use In Sickle Cell Disease Management; Trends And Perspectives In Sub-Saharan Africa.
Inpatient mortality and postpartum readmission rates in sickle cell disease pregnancies: a multistate analysis, 2007-2014.
Livedoid Vasculopathy Presenting in a Patient With Sickle Cell Disease.
Loss of Bone in Sickle Cell Trait and Sickle Cell Disease Female Mice Is Associated With Reduced IGF-1 in Bone and Serum.
Morphological features of the human umbilical vein in normal, sickle cell trait, and sickle cell disease pregnancies.
Newborn Screening for Sickle Cell Disease in Liberia: A Pilot Study.
Newborn screening for sickle cell disease: an innovative pilot program to improve child survival in Dar es Salaam, Tanzania.
Obstetrician-gynecologists' knowledge of sickle cell disease screening and management.
Optical characterization of red blood cells from individuals with sickle cell trait and disease in Tanzania using quantitative phase imaging.
Overactive bladder in adults with sickle cell disease.
Plasma Lipids and Lipoproteins in Sickle Cell Disease Patients in the Northern West Bank, Palestine.
Premarital genetic screening and care of Tanzanian children with sickle cell disease: a qualitative study on parents' views and experiences.
Preoperative screening for sickle cell disease in children: clinical implications.
Prevalence of mitral valve prolapse in Saudi sickle cell disease patients in Dammam - A prospective-controlled echocardiographic study.
Prevalence of sickle cell disease in a northeastern region of the Democratic Republic of Congo: what impact on transfusion policy?
Pulmonary hypertension in sickle cell hemoglobinopathy: a clinicopathologic study of 20 cases.
Recommendations for the management of sickle cell disease in South Africa.
Reproductive attitudes and behaviors in people with sickle cell disease or sickle cell trait: a qualitative interpretive meta-synthesis.
Severity in phenotypic expression of homozygous sickle cell disease (Hb.SS) - Does hypermelanotic or hypomelanotic skin status of affected patients play a role?
Sickle cell anemia and hematological neoplasias.
Sickle cell carriers' unmet information needs: Beyond knowing trait status.
Sickle cell disease and pregnancy outcomes: a study of the community-based hospital in a tribal block of Gujarat, India.
Sickle cell disease in pregnancy: trend and pregnancy outcomes at a tertiary hospital in Tanzania.
Sickle cell disease promotes sex-dependent pathological bone loss through enhanced cathepsin proteolytic activity.
Sickle cell disease resulting from uniparental disomy in a child who inherited sickle cell trait.
Sickle cell trait diagnosis: clinical and social implications.
Significant prevalence of sickle cell disease in Southwest Germany: results from a birth cohort study indicate the necessity for newborn screening.
Situational Analysis of Sickle Cell Disease in Gujarat, India.
Soluble CD163 in young sickle cell disease patients and their trait siblings: a biomarker for pulmonary hypertension and vaso-occlusive complications.
Tartrate-Resistant Acid Phosphatase 5b in Young Patients With Sickle Cell Disease and Trait Siblings: Relation to Vasculopathy and Bone Mineral Density.
Thrombophilic mutations among Southern Iranian patients with sickle cell disease: high prevalence of factor V Leiden.
[Neonatal screening of sickle cell disease in the Balearic Islands Autonomous Community. Pilot study in anonymous unrelated population.]
Siderosis
Assessing cardiac and liver iron overload in chronically transfused patients with sickle cell disease.
Decreased bone mineral density in prepubertal children with sickle cell disease: correlation with growth parameters, degree of siderosis and secretion of growth factors.
Myocardial Iron Overload in Sickle Cell Disease: A Rare But Potentially Fatal Complication of Transfusion.
The relationships between pancreatic T2* values and pancreatic iron loading with cardiac dysfunctions,  hepatic and cardiac iron siderosis among Egyptian children and young adults with β-thalassaemia major and sickle cell disease: a cross-sectional study.
Sinus Thrombosis, Intracranial
Neurologic complications in children under five years with sickle cell disease.
Skin Diseases
Obesity resistance of the stearoyl-CoA desaturase-deficient (scd1-/-) mouse results from disruption of the epidermal lipid barrier and adaptive thermoregulation.
Skin Neoplasms
Hydroxyurea for the treatment of sickle cell disease.
Sleep Apnea Syndromes
An association between right ventricular dysfunction and sudden cardiac death.
Association Between Periodic Limb Movements in Sleep and Cerebrovascular Changes in Children With Sickle Cell Disease.
Cardiac autonomic control in Brugada syndrome patients during sleep: The effects of sleep disordered breathing.
Chronic Pulmonary Complications of Sickle Cell Disease.
Does Obstructive Sleep Apnea Increase Cognitive Deficits in Pediatric Sickle Cell Disease?
Identifying Clinical and Research Priorities in Sickle Cell Lung Disease. An Official American Thoracic Society Workshop Report.
Left ventricular hypertrophy and diastolic dysfunction in children with sickle cell disease are related to asleep and waking oxygen desaturation.
Left Ventricular Structural and Functional Changes in Children With ?-Thalassemia and Sickle Cell Disease: Relationship to Sleep-disordered Breathing.
Nocturnal enuresis in sickle cell disease.
Polysomnographic characteristics of a referred sample of children with sickle cell disease.
Screening for Obstructive Sleep Apnea in Children With Sickle Cell Disease: A Pilot Study.
Sleep Apnea and Sudden Cardiac Death.
Sleep patterns in pediatric sickle cell disease.
Sleep-disordered breathing and nocturnal hypoxemia in young adults with sickle cell disease.
Sudden cardiac death during nighttime hours.
Sleep Apnea, Obstructive
Cost-effectiveness of adenotonsillectomy in reducing obstructive sleep apnea, cerebrovascular ischemia, vaso-occlusive pain, and ACS episodes in pediatric sickle cell disease.
Elevation of tricuspid regurgitant jet velocity, a marker for pulmonary hypertension in children with sickle cell disease.
Headache in children with sickle cell disease: prevalence and associated factors.
Obstructive Sleep Apnea in Patients with Congenital Long QT Syndrome: Implications for Increased Risk of Sudden Cardiac Death.
Pulmonary hypertension in children and adolescents with sickle cell disease.
Severity of obstructive sleep apnea in children with sickle cell disease.
Sleep phenotype in the Townes mouse model of sickle cell disease.
[Pulmonary complications of sickle cell disease in children].
Sleep Deprivation
One-night sleep deprivation induces changes in the DNA methylation and serum activity indices of stearoyl-CoA desaturase in young healthy men.
Sleep Initiation and Maintenance Disorders
Acute Pain and Depressive Symptoms: Independent Predictors of Insomnia Symptoms among Adults with Sickle Cell Disease.
Older Adults' Subjective Cognitive Decline Correlated with Subjective but Not Objective Sleep: A Mediator Role of Depression.
Prevalence and persistence of sleep complaints in a rural older community sample: the MoVIES project.
Psychometric Validation of the Insomnia Severity Index in Adults with Sickle Cell Disease.
The frequency of sleep medication use and the risk of subjective cognitive decline (SCD) or SCD with functional difficulties in elderly individuals without dementia.
The relationship of sleep duration and insomnia to risk of hypertension incidence: a meta-analysis of prospective cohort studies.
Sleep Wake Disorders
Clinical Characteristics in Subjective Cognitive Decline with and without Worry: Baseline Investigation of the SILCODE Study.
Psychosocial and affective comorbidities in sickle cell disease.
Sleep patterns in pediatric sickle cell disease.
Small Cell Lung Carcinoma
[Report of a case of small cell lung cancer associated with Lambert-Eaton myasthenic syndrome and subacute cerebellar degeneration--with a review of the Japanese literature]
Solitary Kidney
Outcomes of dual adult kidney transplants in the United States: an analysis of the OPTN/UNOS database.
Spasm
Optimal Medications and Appropriate Implantable Cardioverter-defibrillator Shocks in Aborted Sudden Cardiac Death Due to Coronary Spasm.
Questionnaire in patients with aborted sudden cardiac death due to coronary spasm in Japan.
Subcutaneous implantable cardioverter-defibrillator implantation for ventricular fibrillation caused by coronary artery spasm: a case report.
Sudden cardiac death from coronary artery spasm in a healthy subject.
Sudden coronary death in the young: Evidence of contractile phenotype of smooth muscle cells in the culprit atherosclerotic plaque.
Ventricular fibrillation survivor due to painless multiple spasm including left main trunk: is the subcutaneous implantable cardioverter-defibrillator necessary?
Spastic Paraplegia, Hereditary
[Spinocerebellar degeneration in Japan--the feature from an epidemiological study]
[Study on argyrophilic inclusions of multisystem atrophy (Oppenheimer)]
Specific Language Disorder
Cerebral blood flow velocity and language functioning in pediatric sickle cell disease.
Spinal Cord Diseases
Copper deficiency myelopathy and subacute combined degeneration of the cord - why is the phenotype so similar?
Functional outcomes in geriatric patients with spinal cord injuries at a tertiary care rehabilitation hospital in Saudi Arabia.
Subacute Combined Degeneration Caused by Nitrous Oxide Intoxication: A Report of Two Cases.
[A case of subacute combined degeneration of the spinal cord diagnosed by characteristic findings of magnetic resonance imaging: case report and review of 22 cases]
Spinal Cord Injuries
Prevalence of spinal cord disorders in Al-Quseir City, Red Sea Governorate, Egypt.
Subacute combined degeneration mimicking traumatic spinal cord injury.
Spinal Stenosis
Judicious and Vigilant Use of Electronically Based Treatment Enhancements and Subjective Patient-Reported Outcomes: Commentary on an article by Richard L. Skolasky, ScD, et al.: "Telephone-Based Intervention to Improve Rehabilitation Engagement After Spinal Stenosis Surgery. A Prospective Lagged Controlled Trial".
Prevalence of vitamin B12 deficiency in spinal cord injury.
Spinocerebellar Ataxias
Cognitive impairment in spinocerebellar degeneration.
Compound heterozygous intermediate MJD alleles cause cerebellar ataxia with sensory neuropathy.
Diffusion- and T2-weighted MRI of the transverse pontine fibres in spinocerebellar degeneration.
Distinguishing spinocerebellar ataxia with pure cerebellar manifestation from multiple system atrophy (MSA-C) through saccade profiles.
["Time, place and person" and neurology]
[A case of spinocerebellar ataxia type 3 (SCA3) associated with isolated ACTH deficiency]
[Overview of Hereditary Spinocerebellar Ataxias in Japan].
[Study of oculomotor disorders in spinocerebellar ataxia genotype]
Spinocerebellar Degenerations
Diffusion- and T2-weighted MRI of the transverse pontine fibres in spinocerebellar degeneration.
Frequency analyses of posturography using logarithmic translation.
Vestibular evoked myogenic potentials in patients with spinocerebellar degeneration.
[Cerebello-cerebral functional relationship in spinocerebellar degeneration using positron emission tomography]
[Study on argyrophilic inclusions of multisystem atrophy (Oppenheimer)]
Splenic Infarction
Anaesthetic implications of laparoscopic splenectomy in patients with sickle cell anaemia.
Splenectomy for hematological diseases: The Qatif Central Hospital experience.
Splenic sepsis in sickle cell disease.
Squamous Cell Carcinoma of Head and Neck
Chronic exposure to chewing tobacco selects for overexpression of stearoyl-CoA desaturase in normal oral keratinocytes.
FADS1 rs174549 Polymorphism May Predict a Favorable Response to Chemoradiotherapy in Oral Cancer Patients.
ST Elevation Myocardial Infarction
A Common Variant in SCN5A and the Risk of Ventricular Fibrillation Caused by First ST-Segment Elevation Myocardial Infarction.
Role of omega-3 ethyl ester concentrate in reducing sudden cardiac death following myocardial infarction and in management of hypertriglyceridemia: An Indian consensus statement.
Sudden cardiac death after acute ST elevation myocardial infarction: insight from a developing country.
Sudden cardiac death early after ST elevation myocardial infarction with and without severe left ventricular dysfunction.
Thrombus composition in sudden cardiac death from acute myocardial infarction.
Starvation
Fatty acid content and pattern of epididymal and parametrial adipose tissue lipids in streptozotocin (type 1) and Goto-Kakizaki (type 2) diabetic rats.
Role of stearoyl-coenzyme A desaturase in regulating lipid metabolism.
stearoyl-coa 9-desaturase deficiency
Absence of stearoyl-CoA desaturase-1 ameliorates features of the metabolic syndrome in LDLR-deficient mice.
Biochemical and Physiological Function of Stearoyl-CoA Desaturase.
Compensatory increases in tear volume and mucin levels associated with meibomian gland dysfunction caused by stearoyl-CoA desaturase-1 deficiency.
Dyslipidemia and atherosclerosis induced by chronic intermittent hypoxia are attenuated by deficiency of stearoyl coenzyme A desaturase.
GPAT4-Generated Saturated LPAs Induce Lipotoxicity through Inhibition of Autophagy by Abnormal Formation of Omegasomes.
Hepatic stearoyl-CoA desaturase-1 deficiency protects mice from carbohydrate-induced adiposity and hepatic steatosis.
Mutants of Bacillus species isolated on the basis of protonophore resistance are deficient in fatty acid desaturase activity.
Reduced adiposity and liver steatosis by stearoyl-CoA desaturase deficiency are independent of peroxisome proliferator-activated receptor-alpha.
Stearoyl-CoA desaturase 1 deficiency elevates insulin-signaling components and down-regulates protein-tyrosine phosphatase 1B in muscle.
Stearoyl-CoA desaturase 1 deficiency increases CTP:choline cytidylyltransferase translocation into the membrane and enhances phosphatidylcholine synthesis in liver.
Stearoyl-CoA desaturase 1 deficiency increases fatty acid oxidation by activating AMP-activated protein kinase in liver.
Stearoyl-CoA desaturase 1 deficiency increases insulin signaling and glycogen accumulation in brown adipose tissue.
Stearoyl-CoA desaturase 1 deficiency protects mice from immune-mediated liver injury.
Stearoyl-CoA desaturase 1 deficiency reduces lipid accumulation in the heart by activating lipolysis independently of peroxisome proliferator-activated receptor ?.
Stearoyl-CoA desaturase deficiency, hypercholesterolaemia, cholestasis and diabetes.
Stearoyl-CoA desaturase deficiency, hypercholesterolemia, cholestasis, and diabetes.
Stearoyl-CoA desaturase-1 deficiency attenuates obesity and insulin resistance in leptin-resistant obese mice.
Stearoyl-CoA desaturase-1 deficiency reduces ceramide synthesis by downregulating serine palmitoyltransferase and increasing beta-oxidation in skeletal muscle.
Stillbirth
Cerebro-placental ratio as a prognostic factor of fetal outcome in pregnancy complicated by maternal sickle cell disease.
Challenges in the management of sickle cell disease during pregnancy in Senegal, West Africa.
Sickle cell disease in pregnancy: trend and pregnancy outcomes at a tertiary hospital in Tanzania.
Stomach Neoplasms
Cancer cell dependence on unsaturated fatty acids implicates stearoyl-CoA desaturase as a target for cancer therapy.
Polyunsaturated fatty acid biosynthesis pathway determines ferroptosis sensitivity in gastric cancer.
Stearoyl-CoA desaturase 1 (SCD1) facilitates the growth and anti-ferroptosis of gastric cancer cells and predicts poor prognosis of gastric cancer.
Subacute combined degeneration without nutritional anemia.
UBE2C Is a Potential Biomarker of Intestinal-Type Gastric Cancer With Chromosomal Instability.
Striatonigral Degeneration
[Spinocerebellar degeneration in Japan--the feature from an epidemiological study]
Stroke
A brief review of the pathophysiology, associated pain, and psychosocial issues in sickle cell disease.
A critical assessment of transcranial doppler screening rates in a large pediatric sickle cell center: opportunities to improve healthcare quality.
A hemoglobin-based multifunctional therapeutic: polynitroxylated pegylated hemoglobin.
Abnormal cranial magnetic resonance imaging scans in sickle-cell disease. Neurological correlates and clinical implications.
Abnormalities in aortic properties: a potential link between left ventricular diastolic function and ventricular-aortic coupling in sickle cell disease.
Acute silent cerebral ischemia and infarction during acute anemia in children with and without sickle cell disease.
Adenylyl Cyclase 9 Polymorphisms Reveal Potential Link to HDL Function and Cardiovascular Events in Multiple Pathologies: Potential Implications in Sickle Cell Disease.
Adverse neurological outcomes in Nigerian children with sickle cell disease.
Allogenic hematopoietic stem cell transplantation in sickle cell disease.
Ambulatory Hypertension in Pediatric Patients With Sickle Cell Disease and Its Association With End-Organ Damage.
An evidence-based approach to the treatment of adults with sickle cell disease.
Angiotensinogen M235T Gene Polymorphism is a Genetic Determinant of Cerebrovascular and Cardiopulmonary Morbidity in Adolescents with Sickle Cell Disease.
Annual stroke incidence in Nigerian children with sickle cell disease and elevated TCD velocities treated with hydroxyurea.
Arterial Stiffness Impairment in Sickle Cell Disease Associated with Chronic Vascular Complications: The Multinational African CADRE Study.
Arteriopathy Influences Pediatric Ischemic Stroke Presentation, but Sickle Cell Disease Influences Stroke Management.
Association between clinical outcomes and metformin use in adults with sickle cell disease and diabetes mellitus.
Association of Silent Cerebrovascular Disease Identified Using Natural Language Processing and Future Ischemic Stroke.
Association of Testosterone Replacement With Cardiovascular Outcomes Among Men With Androgen Deficiency.
Associations Between Transcranial Doppler Flow Velocities, Laboratory Parameters, and Clinical Features in Turkish Children With Sickle Cell Disease.
Asthma management in sickle cell disease.
Asthma management: reinventing the wheel in sickle cell disease.
Big strokes in small persons.
Bone marrow transplantation versus periodic prophylactic blood transfusion in sickle cell patients at high risk of ischemic stroke: a decision analysis.
Brain morphometric analysis predicts decline of intelligence quotient in children with sickle cell disease: A preliminary study.
Brain-derived neurotrophic factor levels in pediatric sickle cell disease.
Can peak systolic velocities be used for prediction of stroke in sickle cell anemia?
Can STOP Trial Velocity Criteria Be Applied to Iranian Children with Sickle Cell Disease?
Cerebral oxygen metabolism in adults with sickle cell disease.
Cerebral Revascularization for Moyamoya Syndrome Associated with Sickle Cell Disease: A Systematic Review of the Literature on the Role of Extracranial-Intracranial Bypass in Treating Neurologic Manifestations of Pediatric Patients with Sickle Cell Disease.
Cerebral Vasoreactivity in Children with Sickle Cell Disease: A Transcranial Doppler Study.
Cerebrovascular disease in symptomatic and asymptomatic patients with sickle cell anemia: screening with duplex transcranial Doppler US--correlation with MR imaging and MR angiography.
Cerebrovascular reserve capacity is impaired in patients with sickle cell disease.
Childhood stroke in Eastern Province, KSA: pattern, risk factors, diagnosis and outcome.
Chronic blood transfusion therapy practices to treat strokes in children with sickle cell disease.
Chronic Disease Management in Sickle Cell Trait Patients in the Primary Care Setting: A Case Report.
Circadian influence on coronary events.
Circulating platelet and erythrocyte microparticles in young children and adolescents with sickle cell disease: Relation to cardiovascular complications.
Clinical Manifestations and Long-Term Mortality in Lamin A/C Mutation Carriers From a Japanese Multicenter Registry.
Clinical predictors of poor outcomes in patients with sickle cell disease and COVID-19 infection.
Clinical, laboratory, and genetic risk factors for thrombosis in sickle cell disease.
Coexistent Sickle Cell Disease Has No Impact on the Safety or Outcome of Lytic Therapy in Acute Ischemic Stroke: Findings From Get With The Guidelines-Stroke.
Cognitive and behavior deficits in sickle cell mice are associated with profound neuropathologic changes in hippocampus and cerebellum.
Cognitive and behavioral function in children with sickle cell disease: a review and discussion of methodological issues.
Cognitive screening examinations for silent cerebral infarcts in sickle cell disease.
Common Complications of Sickle Cell Disease: A Simulation-Based Curriculum.
Comorbid Chronic Conditions Among Older Adults with Subjective Cognitive Decline, United States, 2015-2017.
Contribution of sickle cell disease to the occurrence of developmental disabilities: a population-based study.
Contribution of sickle cell disease to the pediatric stroke burden among hospital discharges of African-Americans-United States, 1997-2012.
Correlation of abnormal intracranial vessel velocity, measured by transcranial Doppler ultrasonography, with abnormal conjunctival vessel velocity, measured by computer-assisted intravital microscopy, in sickle cell disease.
Correlation of the C677T MTHFR genotype with homocysteine levels in children with sickle cell disease.
Curing Hemoglobinopathies: Challenges and Advances of Conventional and New Gene Therapy Approaches.
Current concepts in the management of stroke in children with sickle cell disease.
Current issues in blood transfusion for sickle cell disease.
Daily peaks in the incidence of sudden cardiac death and fatal stroke in Niigata Prefecture.
Declining stroke rates in Californian children with sickle cell disease.
Decreased cerebral perfusion correlates with increased BOLD hyperoxia response in transgenic mouse models of sickle cell disease.
Deferasirox for managing transfusional iron overload in people with sickle cell disease.
Detection and assessment of stroke in patients with sickle cell disease: neuropsychological functioning and magnetic resonance imaging.
Distribution of sickle cell disease and assessment of risk factors based on transcranial Doppler values in the Gulf region.
Does regular blood transfusion prevent progression of cerebrovascular lesions in children with sickle cell disease?
Dural Venous Sinus Diameters in Children with Sickle Cell Disease: Correlation with History of Stroke in a Case-Control Study.
Dynamic vascular analysis shows a hyperemic flow pattern in sickle cell disease.
ECG-based cardiac screening programs: Legal, ethical, and logistical considerations.
Effect of Chronic Blood Transfusion on Biomarkers of Coagulation Activation and Thrombin Generation in Sickle Cell Patients at Risk for Stroke.
Effect of chronic red cell transfusion therapy on vasculopathies and silent infarcts in patients with sickle cell disease.
Effect of transfusion therapy on transcranial doppler ultrasonography velocities in children with sickle cell disease.
Electroencephalography hyperventilation and stroke in children with sickle cell disease.
Elevated plasma sVCAM-1 levels in children with sickle cell disease: impact of chronic transfusion therapy.
Emergency Medicine Management of Sickle Cell Disease Complications: An Evidence-Based Update.
Encephaloduroarteriosynangiosis (EDAS) in young patients with cerebrovascular complications of sickle cell disease: Single-institution experience.
Encephaloduroarteriosynangiosis and encephalomyoarteriosynangiosis for treatment of moyamoya syndrome in pediatric patients with sickle cell disease.
Evaluation of transcranial Doppler abnormalities in children with sickle cell disease in El-Obeid Specialized Children's Hospital.
Evidence of cranial artery ectasia in sickle cell disease patients with ectasia of the basilar artery.
Feasibility and efficacy of chronic transfusion for stroke prevention in children with sickle cell disease.
Five years of experience with hydroxyurea in children and young adults with sickle cell disease.
Frequent red cell transfusions reduced vascular endothelial activation and thrombogenicity in children with sickle cell anemia and high stroke risk.
Functional outcomes of children with sickle-cell disease affected by stroke.
Gene coexpression networks analysis of sickle stroke risk.
Genetic determinants and stroke in children with sickle cell disease.
Genetic modifiers of severity in sickle cell disease.
Genetic modifiers of the beta-haemoglobinopathies.
Genetics of Sickle Cell-Associated Cardiovascular Disease: An Expert Review with Lessons Learned in Africa.
Genomic polymorphisms in sickle cell disease: implications for clinical diversity and treatment.
Global Electric Heterogeneity Risk Score for Prediction of Sudden Cardiac Death in the General Population: The Atherosclerosis Risk in Communities (ARIC) and Cardiovascular Health (CHS) Studies.
Hematologic risk factors for stroke in Saudi children.
Hemoglobinopathies and Stroke: Strategies for Prevention and Treatment.
HLA-DRB1 alleles in Hb SS patients with avascular necrosis of the femoral head.
Homocysteine in sickle cell disease: relationship to stroke.
How I treat and manage strokes in sickle cell disease.
Hydroxyurea as an alternative to blood transfusions for the prevention of recurrent stroke in children with sickle cell disease.
Hydroxyurea can be used in children with sickle cell disease and cerebral vasculopathy for the prevention of chronic complications? A meta-analysis.
Hydroxyurea for sickle cell disease in children and for prevention of cerebrovascular events: the Belgian experience.
Hydroxyurea therapy lowers TCD velocities in children with sickle cell disease.
Hydroxyurea Use Associated with Nonverbal and Executive Skills in Sickle Cell Anemia.
Imaging review of sickle cell disease for the emergency radiologist.
Inadequate community knowledge about sickle cell disease among African-American women.
Incidence and Predictors of Sudden Cardiac Death After a Major Non-Fatal Cardiovascular Event.
Increased complications of chronic erythrocytapheresis compared with manual exchange transfusions in children and adolescents with sickle cell disease.
Increased von Willebrand factor antigen and high molecular weight multimers in sickle cell disease associated with nocturnal hypoxemia.
Inflammation in sickle cell disease.
Influence of beta-cluster haplotypes, alpha-gene status and UGTA1 polymorphism on clinical and hematological data in sickle-cell disease children from French Guiana.
Inherited DNA mutations contributing to thrombotic complications in patients with sickle cell disease.
Integrated psychology support and comprehensive cognitive evaluation improves access to special education services for children with sickle cell disease.
Interleukin-1 receptor inhibition reduces stroke size in a murine model of sickle cell disease.
Intra-individual variation in blood flow velocities in cerebral arteries of children with sickle cell disease.
Is Chlamydia pneumoniae infection associated with stroke in children with sickle cell disease?
Knowledge and Health Beliefs Regarding Sickle Cell Disease Among Omanis in a Primary Healthcare Setting: Cross-sectional study.
Knowledge of stroke risk, signs of stroke, and the need for stroke education among children with sickle cell disease and their caregivers.
Laboratory Biomarkers, Cerebral Blood Flow Velocity, and Intellectual Function in Children with Sickle Cell Disease.
Large-vessel occlusion in sickle cell disease: pathogenesis, clinical consequences, and therapeutic implications.
Life threatening parvovirus B19 and herpes simplex virus associated acute myocardial dysfunction in a child with homozygous sickle cell disease.
Long Term Outcome and Evaluation of Organ Function in Pediatric Patients Undergoing Haploidentical and Matched Related Hematopoietic Cell Transplantation for Sickle Cell Disease.
Long-term results of related myeloablative stem-cell transplantation to cure sickle cell disease.
Management and outcomes of hypertrophic cardiomyopathy in young adults.
Measuring Pain in Sickle Cell Disease using Clinical Text.
Mechanisms of vasculopathy in sickle cell disease and thalassemia.
Microfluidics in Sickle Cell Disease Research: State of the Art and a Perspective Beyond the Flow Problem.
Modes of death and clinical outcomes in adult patients with hypertrophic cardiomyopathy in Thailand.
Mortality in Individuals with Subjective Cognitive Decline: Results of the Leipzig Longitudinal Study of the Aged (LEILA75+).
Mortality in sickle cell disease: A population-based study in an aboriginal community in the Gudalur Valley, Nilgiris, Tamil Nadu, India.
mTOR Inhibition Improves Anaemia and Reduces Organ Damage in a Murine Model of Sickle Cell Disease.
Multivariate surface-based analysis of corpus callosum in patients with sickle cell disease.
National registry of hemoglobinopathies in Spain (REPHem).
Need for cognitive rehabilitation for children with sickle cell disease and strokes.
Neurologic and Cognitive Outcomes in Sickle Cell Disease from Infancy through Adolescence.
Neurologic complications of sickle cell disease.
Neurological PRESentations in Sickle Cell Patients Are Not Always Stroke: A Review of Posterior Reversible Encephalopathy Syndrome in Sickle Cell Disease.
Neurological soft signs as the stroke risk in sickle cell disease.
Neuropsychological aspects of pediatric sickle cell disease.
Neuropsychological functioning in preschool-age children with sickle cell disease: the role of illness-related and psychosocial factors.
Neuropsychological functioning of youths with sickle cell disease: comparison with non-chronically ill peers.
New approaches to hematopoietic cell transplantation for hematological diseases in children.
Nocturnal hypertension associated with stroke and silent cerebral infarcts in children with sickle cell disease.
Nocturnal oxyhemoglobin desaturation and arteriopathy in a pediatric sickle cell disease cohort.
Non-fatal cardiovascular events preceding sudden cardiac death in patients with an acute myocardial infarction complicated by heart failure: insights from the high-risk myocardial infarction database.
Noninvasive optical assessment of resting-state cerebral blood flow in children with sickle cell disease.
Oral contraceptive use and incident stroke in women with sickle cell disease.
Out with the bad and in with the good; red cell exchange, white cell reduction, and platelet reduction.
Outcome of Pregnancy in Saudi Women with Sickle Cell Disease Attending the Tertiary Care University Hospital in Eastern Province of Saudi Arabia.
Paediatric sickle cell disease: pulmonary hypertension but normal vascular resistance.
Patent foramen ovale in patients with sickle cell disease and stroke: case presentations and review of the literature.
Pathophysiology of stroke in sickle cell disease.
Patients with sickle cell disease are frequently excluded from the benefits of transcranial doppler screening for the risk of stroke despite extensive and compelling evidence.
Pattern of Cerebral Blood Flow Velocity Using Transcranial Doppler Ultrasonography in Children with Sickle Cell Disorder in Lagos State, Nigeria.
Pediatric Neurodevelopmental Delays in Children 0 to 5 Years of Age With Sickle Cell Disease: A Systematic Literature Review.
Peer relationships and emotional well-being of children with sickle cell disease: a controlled replication.
Perioperative Management of Sickle Cell Disease.
Plasma glial fibrillary acidic protein levels in a child with sickle cell disease and stroke.
Platelets, coagulation, and fibrinolysis in sickle cell disease: their possible role in vascular occlusion.
Polymorphisms within the angiotensinogen gene (GT-repeat) and the risk of stroke in pediatric patients with sickle cell disease: a case-control study.
Practice Patterns of Stroke Screening and Hydroxyurea Use in Children With Sickle Cell Disease: A Survey of Health Care Providers.
Predictive validity of developmental screening in young children with sickle cell disease: a longitudinal follow-up study.
Preliminary study of working memory in children with stroke related to sickle cell disease.
Prevalence of intracardiac shunting in children with sickle cell disease and stroke.
Prevention of central nervous system sequelae in sickle cell disease without evidence from randomized controlled trials: the case for a team-based learning collaborative.
Prevention of stroke in sickle cell anemia.
Primary and Secondary Stroke Prevention in Children With Sickle Cell Disease.
Primary stroke prevention for sickle cell disease in north-east Italy: the role of ethnic issues in establishing a Transcranial Doppler screening program.
Process mapping of the urgent red cell exchange procedure for patients with severe complications of sickle cell disease at a centralized hemapheresis service.
Prognostic role of left ventricular apical aneurysm in hypertrophic cardiomyopathy: A systematic review and meta-analysis.
Prothrombin mutant, factor V Leiden, and thermolabile variant of methylenetetrahydrofolate reductase among patients with sickle cell disease in Brazil.
Quality of life among children with sickle cell disease receiving chronic transfusion therapy.
Quantitative MR imaging of children with sickle cell disease: striking T1 elevation in the thalamus.
Racial and ethnic differences in post-stroke subjective cognitive decline exist.
Racial and ethnic disparities in subjective cognitive decline: a closer look, United States, 2015-2018.
Racial differences in sudden cardiac death among hypertensive patients during antihypertensive therapy: The LIFE study.
Red blood cell transfusion to treat or prevent complications in sickle cell disease: an overview of Cochrane reviews.
Red Blood Cells: Exchange, Transfuse, or Deplete.
Regional cerebral blood flow in patients with sickle cell disease: study with single photon emission computed tomography.
Regional oxygen extraction predicts border zone vulnerability to stroke in sickle cell disease.
Regular transfusion lowers plasma free hemoglobin in children with sickle-cell disease at risk for stroke.
Relation of atrial and/or ventricular premature complexes on a two-minute rhythm strip to the risk of sudden cardiac death (the Atherosclerosis Risk in Communities [ARIC] study).
Relationship of Sudden Cardiac Death to New-Onset Atrial Fibrillation in Hypertensive Patients with Left Ventricular Hypertrophy.
Removal of Arterial Vessel Contributions in Susceptibility-Weighted Images for Quantification of Normalized Visible Venous Volume in Children with Sickle Cell Disease
Removal of Arterial Vessel Contributions in Susceptibility-Weighted Images for Quantification of Normalized Visible Venous Volume in Children with Sickle Cell Disease.
Risk of recurrent stroke in children with sickle cell disease receiving blood transfusion therapy for at least five years after initial stroke.
Role of positron emission tomography in determining the extent of CNS ischemia in patients with sickle cell disease.
SCD in the world, Europe, Bosnia and Herzegovina and Mostar.
Secondary prevention of overt strokes in sickle cell disease: therapeutic strategies and efficacy.
Sickle cell disease and H3Africa: enhancing genomic research on cardiovascular diseases in African patients.
Sickle cell disease and stroke.
Sickle cell disease as a vascular disorder.
Sickle cell disease in children.
Sickle cell disease mice have cerebral oxidative stress and vascular and white matter abnormalities.
Sickle cell disease subphenotypes in patients from southwestern province of saudi arabia.
Sickle cell disease.
Sickle cell disease: current activities, public health implications, and future directions.
Sickle cell disease: management options and challenges in developing countries.
Sickle cell disease: primary stroke prevention.
Sickle Cell Disease: Reference Values and Interhemispheric Differences of Nonimaging Transcranial Doppler Blood Flow Parameters.
Sickle cell disease: Translating clinical care to low-resource countries through international research collaborations.
Sickle cell disease: when and how to transfuse.
Sickle cell leg ulcers: a frequently disabling complication and a marker of severity.
Silent cerebral infarcts occur despite regular blood transfusion therapy after first stroke in children with sickle cell disease.
Silent infarction as a risk factor for overt stroke in children with sickle cell anemia: a report from the Cooperative Study of Sickle Cell Disease.
Sleep-disordered breathing and comorbidities: role of the upper airway and craniofacial skeleton.
Soluble CD163 in young sickle cell disease patients and their trait siblings: a biomarker for pulmonary hypertension and vaso-occlusive complications.
Soluble receptor for advanced glycation end products as a vasculopathy biomarker in sickle cell disease.
Stable to improved cardiac and pulmonary function in children with high-risk sickle cell disease following haploidentical stem cell transplantation.
Stroke and presence of patent foramen ovale in sickle cell disease.
Stroke in sickle cell disease in Africa: case report.
Stroke Prevalence in Children With Sickle Cell Disease in Sub-Saharan Africa: A Systematic Review and Meta-Analysis.
Stroke prevention and treatment in sickle cell disease.
Stroke recurrence in children with sickle cell disease treated with hydroxyurea following first clinical stroke.
Subtle brain abnormalities in children with sickle cell disease: relationship to blood hematocrit.
Subtle neuropsychological deficits in children with sickle cell disease.
Successful matched sibling donor marrow transplantation following reduced intensity conditioning in children with hemoglobinopathies.
Temporal distribution of death among oncology patients: environmental links.
The cause of the stroke: a diagnostic uncertainty.
The clinical effectiveness and cost-effectiveness of primary stroke prevention in children with sickle cell disease: a systematic review and economic evaluation.
The cognitive and academic impact of sickle cell disease.
The Economic Burden of End-Organ Damage Among Medicaid Patients with Sickle Cell Disease in the United States: A Population-Based Longitudinal Claims Study.
The effect of a sequential compression device on hemodynamics in arthroscopic shoulder surgery using beach-chair position.
The epidemiology of stroke in sickle cell patients in Yaounde, Cameroon.
The excess burden of stroke in hospitalized adults with sickle cell disease.
The Genetic Landscape of Cerebral Steno-Occlusive Arteriopathy and Stroke in Sickle Cell Anemia.
The glomerulopathy of sickle cell disease.
The interaction between sickle cell disease and HIV infection: a systematic review.
The Other Side of Abnormal: A Case Series of Low Transcranial Doppler Velocities Associated With Stroke in Children With Sickle Cell Disease.
The radiological manifestations of sickle cell disease.
The relationship between white matter microstructure and self-perceived cognitive decline.
The Role of Inflammation and Leukocytes in the Pathogenesis of Sickle Cell Disease.
The Role of Inflammation and Leukocytes in the Pathogenesis of Sickle Cell Disease; Haemoglobinopathy.
The role of MRA in pediatric sickle cell disease with normal transcranial Doppler imaging velocities.
The role of religious leaders and faith organisations in haemoglobinopathies: a review.
The use of extracorporeal membrane oxygenation in pediatric patients with sickle cell disease.
Thromboinflammatory mechanisms in sickle cell disease - challenging the hemostatic balance.
Thyroid-stimulating hormone and risk of sudden cardiac death, total mortality and cardiovascular morbidity.
Tract-specific analysis and neurocognitive functioning in sickle cell patients without history of overt stroke.
Transcranial color Doppler in stroke-free adult patients with sickle cell disease.
Transcranial Doppler in adult patients with sickle cell disease.
Transcranial Doppler screening for stroke risk in children with sickle cell disease: a systematic review.
Transcranial Doppler screening in Nigerian children with sickle cell disease: A 10-year longitudinal study on the SPPIBA cohort.
Transcranial Doppler ultrasonography in adults with sickle cell disease.
Transcranial Doppler ultrasonography in siblings with sickle cell disease.
Transition and sickle cell disease.
Transplantation of unrelated placental blood cells in children with high-risk sickle cell disease.
Treatment and prevention of cerebrovascular disorders in children.
Treatment and prevention of stroke in children with sickle cell disease.
Treatment-related Correlates of Growth in Children With Sickle Cell Disease in the DISPLACE Cohort.
Trends in comorbid sickle cell disease among stroke patients.
Unrelated cord blood transplantation in children with sickle cell disease: review of four-center experience.
Use of Pleuroperitoneal Shunt in Chylothorax Related to Central Line Associated Thrombosis in Sickle Cell Disease.
Utilizing Whole-Exome Sequencing to Characterize the Phenotypic Variability of Sickle Cell Disease.
Validation of the Burden Index of Caregivers (BIC), a multidimensional short care burden scale from Japan.
Value of the QRS-T area angle in improving the prediction of sudden cardiac death after acute coronary syndromes.
Vascular Instability and Neurological Morbidity in Sickle Cell Disease: An Integrative Framework.
Vitamin D deficiency is associated with sudden cardiac death, combined cardiovascular events, and mortality in haemodialysis patients.
White matter has impaired resting oxygen delivery in sickle cell patients.
[Acute encephalic manifestations in Senegalese children with sickle cell disease]
[Blood transfusion assessment to 112 homozygous sickle-cell disease patients in university hospital of Brazzaville.]
[Screening of cerebral vasculopathy in sickle cell anemia children using transcranial Doppler].
[Stroke prevention in sickle-cell disease: results, hurdles and future perspectives]
Stuttering
Ischemic priapism in South-East Nigeria: Presentation, management challenges, and aftermath issues.
Medical management of ischemic stuttering priapism: a contemporary review of the literature.
Men with sickle cell disease experience greater sexual dysfunction when compared with men without sickle cell disease.
Priapism and Sickle-Cell Anemia: Diagnosis and Nonsurgical Therapy.
Subacute Combined Degeneration
Clinical and imaging characteristics of subacute combined degeneration complicated with white matter lesions in the brain: a report of five cases.
Subarachnoid Hemorrhage
Distribution of sickle cell disease and assessment of risk factors based on transcranial Doppler values in the Gulf region.
Intracranial aneurysms in sickle cell disease: A systematic review and case-control study.
Intracranial Aneurysms in Sickle-Cell Disease Are Associated With the Hemoglobin SS Genotype But Not With Moyamoya Syndrome.
Intracranial stenting as monotherapy in subarachnoid hemorrhage and sickle cell disease.
Nonaneurysmal Subarachnoid Hemorrhage in Sickle Cell Disease: Description of a Case and a Review of the Literature.
Use of a flow-diverting stent for ruptured dissecting aneurysm treatment in a patient with sickle cell disease.
Sudden Unexpected Death in Epilepsy
Differential Methylation in the GSTT1 Regulatory Region in Sudden Unexplained Death and Sudden Unexpected Death in Epilepsy.
Sudden cardiac death in children and young adults without structural heart disease: a comprehensive review.
Too long or too short? New insights into abnormal cardiac repolarization in people with chronic epilepsy and its potential role in sudden unexpected death.
Supranuclear Palsy, Progressive
Spinocerebellar degeneration: Discrepancies between clinical and pathological diagnoses.
[Study on argyrophilic inclusions of multisystem atrophy (Oppenheimer)]
Syncope
A novel cardiac ryanodine receptor gene (RyR2) mutation in an athlete with aborted sudden cardiac death: a case of adult-onset catecholaminergic polymorphic ventricular tachycardia.
A novel mutation of dipeptidyl aminopeptidase-like protein-6 in a family with suspicious idiopathic ventricular fibrillation.
A Novel Risk Stratification Score for Sudden Cardiac Death Prediction in Middle-Aged, Nonischemic Dilated Cardiomyopathy Patients: The ESTIMATED Score.
A score model to predict risk of events in patients with Brugada Syndrome.
A validation study of the European Society of Cardiology guidelines for risk stratification of sudden cardiac death in childhood hypertrophic cardiomyopathy.
Aborted sudden cardiac death (SCD) in a patient with hypertrophic cardiomyopathy (HCM) with low-risk factors for SCD.
Aborted sudden cardiac death and a mother with suspected metabolic myopathy.
Amiodarone versus other pharmacological interventions for prevention of sudden cardiac death.
Approach to the asymptomatic patients with Brugada syndrome.
Are implantable cardioverter defibrillator shocks a surrogate for sudden cardiac death in patients with nonischemic cardiomyopathy?
Arrhythmic events in Brugada syndrome patients induced by fever.
Arrhythmogenic Right Ventricular Cardiomyopathy: A Review of Living and Deceased Probands.
Arrhythmogenic right ventricular cardiomyopathy: diagnosis and risk stratification.
Arrhythmogenic right ventricular cardiomyopathy: ECG progression over time and correlation with long-term follow-up.
Arrhythmogenic right ventricular dysplasia: a United States experience.
Arrhythmogenic ventricular cardiomyopathy: A paradigm shift from right to biventricular disease.
Assessing QT interval prolongation and its associated risks with antipsychotics.
Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy.
Automated extraction of sudden cardiac death risk factors in hypertrophic cardiomyopathy patients by natural language processing.
Brugada disease: chronology of discovery and paternity. Preliminary observations and historical aspects.
Brugada Phenocopy Induced by Electrolyte Disorder: A Transient Electrocardiographic Sign.
Brugada syndrome 2012.
Brugada syndrome: A general cardiologist's perspective.
Catecholaminergic polymorphic ventricular tachycardia, an update.
Catheter Ablation of Ventricular Tachycardia in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy.
Circadian rhythm dynamics on multiscale entropy identifies autonomic dysfunction associated with risk of ventricular arrhythmias and near syncope in chronic kidney disease.
Clinical and Functional Genetic Characterization of the Role of Cardiac Calcium Channel Variants in the Early Repolarization Syndrome.
Clinical characterisation and long-term prognosis of women with Brugada syndrome.
Congenital short QT syndrome. A review.
Congenital Short QT Syndrome: Landmarks of the Newest Arrhythmogenic Cardiac Channelopathy.
Correlation between the signal-averaged electrocardiogram and electrophysiologic study findings in patients with coronary artery disease and sustained ventricular tachycardia.
Current and state of the art on the electrophysiologic characteristics and catheter ablation of arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Current Management of Anomalous Aortic Origin of a Coronary Artery: A Pan-Canadian Survey.
Diagnosis and management of hypertrophic cardiomyopathy.
Differences in 12-lead electrocardiogram between symptomatic and asymptomatic Brugada syndrome patients.
Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome.
Early Repolarisation Changes in ECG: Are they Benign or Malignant?
Early Repolarization Disease.
Early Repolarization Variant in Syncopal Patients Referred to Tilt Testing.
Electrophysiological and therapeutic implications of cardiac arrhythmias in hypertension.
Evaluation of patients with complex ventricular arrhythmias: current noninvasive and invasive methods.
Gender Difference in Clinical and Genetic Characteristics of Brugada Syndrome: SADS-TW BrS Registry.
Heart rate turbulence and deceleration capacity for risk prediction of serious arrhythmic events in Marfan syndrome.
Hypertrophic cardiomyopathy in a large community-based population: clinical outcome and identification of risk factors for sudden cardiac death and clinical deterioration.
Impact of clinical and genetic findings on the management of young patients with Brugada syndrome.
Implantable cardioverter defibrillator therapy for life-threatening arrhythmias in young patients.
Implantable cardioverter defibrillator therapy in children with long QT syndrome.
Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrest.
Inducibility of life-threatening ventricular arrhythmias is related to maximum left ventricular thickness and clinical markers of sudden cardiac death in patients with hypertrophic cardiomyopathy attributable to the Asp175Asn mutation in the alpha-tropomyosin gene.
Left Ventricular Non-Compaction in Athletes: To Play or Not to Play.
Life-threatening arrhythmias leading to syncope in patients with vasospastic angina.
Long-term follow-up and risk assessment of arrhythmogenic right ventricular dysplasia/cardiomyopathy: personal experience from different primary and tertiary centres.
Long-term prognosis of patients diagnosed with Brugada syndrome: Results from the FINGER Brugada Syndrome Registry.
Long-term prognosis of patients with Brugada syndrome and an implanted cardioverter-defibrillator.
Malignant Dysrhythmias - Brugada Type 1 Pattern Formation in the Presence of Fever.
Management and outcomes of hypertrophic cardiomyopathy in young adults.
Nationwide experience of catecholaminergic polymorphic ventricular tachycardia caused by RyR2 mutations.
Next-generation sequencing identified novel Desmoplakin frame-shift variant in patients with Arrhythmogenic cardiomyopathy.
Non-atherosclerotic coronary artery disease associated with sudden cardiac death.
Noninvasive Predictors of Malignant Arrhythmias.
Orthostatic blood pressure test for risk stratification in patients with hypertrophic cardiomyopathy.
Outcome after implantation of a cardioverter-defibrillator in patients with Brugada syndrome: a multicenter study.
Outcome and complications after implantable cardioverter defibrillator therapy in hypertrophic cardiomyopathy: systematic review and meta-analysis.
Patient understanding of disease and the use and outcome of implantable cardioverter defibrillators in hypertrophic cardiomyopathy.
Preclinical short QT syndrome models: studying the phenotype and drug-screening.
Prediction of arrhythmic events with positron emission tomography: PAREPET study design and methods.
Prediction of the estimated 5-year risk of sudden cardiac death and syncope or non-sustained ventricular tachycardia in patients with hypertrophic cardiomyopathy using late gadolinium enhancement and extracellular volume CMR.
Predictors of right ventricular function and size in patients with hypertrophic cardiomyopathy.
Predictors of sudden cardiac death in hypertrophic cardiomyopathy.
Prevalence of Jervell-Lange Nielsen syndrome in children with congenital bilateral sensorineural hearing loss.
Prognostic impact of misdiagnosis of cardiac channelopathies as epilepsy.
Prophylactic implantation of cardioverter-defibrillator in patients with severe cardiac amyloidosis and high risk for sudden cardiac death.
Prospective risk stratification of sudden cardiac death in Marfan's syndrome.
Recent developments in the management of patients at risk for sudden cardiac death.
Regional prevalence and clinical benefit of implantable cardioverter defibrillators in Brugada syndrome.
Relationship between impaired repolarization parameters and poor cardiovascular clinical outcomes in patients with potentially serious coronary artery anomalies.
Risk factors for cardiac events in patients with Brugada syndrome: A PRISMA-compliant meta-analysis and systematic review.
Risk Markers and Appropriate Implantable Defibrillator Therapy in Hypertrophic Cardiomyopathy.
Risk of Syncope in Family Members Who Are Genotype Negative for a Family-Associated Long QT Syndrome Mutation.
Risk stratification and primary prevention of sudden cardiac death: sudden death prevention.
Risk stratification for sudden cardiac death in hypertrophic cardiomyopathy: systematic review of clinical risk markers.
Risk stratification in arrhythmogenic right ventricular cardiomyopathy.
Risk stratification in pediatric hypertrophic cardiomyopathy: Insights for bridging the evidence gap?
Risk stratification of individuals with the Brugada electrocardiogram: a meta-analysis.
Semi-quantitative versus quantitative assessments of late gadolinium enhancement extent for predicting spontaneous ventricular tachyarrhythmia events in patients with hypertrophic cardiomyopathy.
Sudden arrhythmia death syndrome in young victims: a five-year retrospective review and two-year prospective molecular autopsy study by next-generation sequencing and clinical evaluation of their first-degree relatives.
Sudden cardiac death and the use of implantable cardioverter-defibrillators in pediatric patients. The Pediatric Electrophysiology Society.
Sudden cardiac death in football players: Towards a new pre-participation algorithm.
Sudden cardiac death in Long QT syndrome (LQTS), Brugada syndrome, and catecholaminergic polymorphic ventricular tachycardia (CPVT).
Sudden cardiac death in patients with hypertrophic cardiomyopathy: from bench to bedside with an emphasis on genetic markers.
Syncope and the risk of sudden cardiac death: Evaluation, management, and prevention.
Syncope as a Warning Symptom of Sudden Cardiac Death in Athletes.
Syncope in Primary Prevention Implantable Cardioverter Defibrillator Patients.
The Efficacy of Beta-Blockers in Patients With Long QT Syndrome 1-3 According to Individuals' Gender, Age, and QTc Intervals: A Network Meta-analysis.
The role of ion channelopathies in sudden cardiac death: implications for clinical practice.
The SHIFT model combines clinical, electrocardiographic and echocardiographic parameters to predict sudden cardiac death in hypertrophic cardiomyopathy.
The usefulness of soluble ST2 and galectin-3 as novel biomarkers for better risk stratification in hypertrophic cardiomyopathy.
Unique clinical characteristics and SCN5A mutations in patients with Brugada syndrome in Taiwan.
Usefulness of Electrocardiographic Patterns at Presentation to Predict Long-term Risk of Cardiac Death in Patients With Hypertrophic Cardiomyopathy.
Validation of the HCM Risk-SCD model in patients with hypertrophic cardiomyopathy following alcohol septal ablation.
Ventricular arrhythmias induced by programmed ventricular stimulation after uncomplicated myocardial infarction.
Whole-Exome Sequencing Identifies a Novel Mutation (p.L320R) of Alpha-Actinin 2 in a Chinese Family with Dilated Cardiomyopathy and Ventricular Tachycardia.
[Catecholaminergic polymorphic ventricular tachycardia.]
[Heart Rate Turbulence and T-Wave Alternans as Markers of Risk of Sudden Cardiac Death in Patients With Hypertrophic Cardiomyopathy.]
[Prognostic value of microvolt level T-wave alternans in patients at high risk of sudden cardiac death]
[Sympathetic neurograms in patients with neurodegenerative disorders--an overview]
[The electrophysiological study and implantable cardioverter defibrillator therapy for the patients with Brugada syndrome]
[The role of three-dimensional speckle tracking imaging derived parameters on predicting outcome of hypertrophic cardiomyopathy patients with MYH7 mutations].
[Ventricular tachycardia : Treatment and prognostic significance].
Synucleinopathies
Cell models of lipid-rich ?-synuclein aggregation validate known modifiers of ?-synuclein biology and identify stearoyl-CoA desaturase.
Syphilis
Prevalence of serologic markers of transfusion and sexually transmitted infections and their correlation with clinical features in a large cohort of Brazilian patients with sickle cell disease.
Tachycardia
Brugada syndrome in the young: an assessment of risk factors predicting future events.
Cardiac arrest recorded on ambulatory electrocardiograms.
Clinical management of ventricular tachycardia.
Continuous telemetry from a chronic canine model of sudden cardiac death.
Electrophysiologic Considerations After Sudden Cardiac Arrest.
Emergency department risk factors for serious clinical deterioration in a paediatric hospital in Peru.
Long-term follow-up of adult patients with congenital heart disease and an implantable cardioverter defibrillator.
Mechanism and prediction of sudden cardiac death in arrhythmia patients using electrophysiological studies.
Microvolt T-wave alternans and autonomic nervous system parameters can be helpful in the identification of low-arrhythmic risk patients with ischemic left ventricular systolic dysfunction.
Myocarditis in the Athlete: Arrhythmogenic Substrates, Clinical Manifestations, Management, and Eligibility Decisions.
NOS1AP Polymorphisms Modify QTc Interval Duration But Not Cardiac Arrest Risk in Hypertrophic Cardiomyopathy.
Prediction of sudden death in elderly patients with heart failure.
Proteasome inhibition 1 h following ischemia protects GRK2 and prevents malignant ventricular tachyarrhythmias and SCD in a model of myocardial infarction.
Sudden cardiac death and the use of implantable cardioverter-defibrillators in pediatric patients. The Pediatric Electrophysiology Society.
Supraventricular Arrhythmias in Patients with Adult Congenital Heart Disease.
Temporal distribution of arrhythmic events in chronic kidney disease: Highest incidence in the long interdialytic period.
Wolff Parkinson white pattern in Danon disease: When preexcitation is not what it seems.
[Negative result of microvolt T-wave alternans test is helpful in scheduling the order of cardioverter-defibrillator implantation in primary prevention of sudden cardiac death in individuals with the left ventricular systolic dysfunction].
[Non-pharmacologic prevention of sudden cardiac death]
Tachycardia, Sinus
QT prolongation and sudden cardiac death risk in hypertrophic cardiomyopathy.
Tachycardia, Supraventricular
QT prolongation and sudden cardiac death risk in hypertrophic cardiomyopathy.
Risk of arrhythmia and sudden death in patients with asymptomatic preexcitation: a meta-analysis.
Sudden Cardiac Death in Adult Congenital Heart Disease.
Tachycardia, Ventricular
A 34-year longitudinal study on long-term cardiac outcomes in DM1 patients with normal ECG at baseline at an Italian clinical centre.
A new prediction model for ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy.
A novel cardiac ryanodine receptor gene (RyR2) mutation in an athlete with aborted sudden cardiac death: a case of adult-onset catecholaminergic polymorphic ventricular tachycardia.
A Novel Risk Stratification Score for Sudden Cardiac Death Prediction in Middle-Aged, Nonischemic Dilated Cardiomyopathy Patients: The ESTIMATED Score.
A validation study of the European Society of Cardiology guidelines for risk stratification of sudden cardiac death in childhood hypertrophic cardiomyopathy.
AANA Journal Course: update for nurse anesthetists--management of malignant ventricular tachyarrhythmias: the role of drug therapy and surgical intervention in sudden cardiac death survivors.
Abnormalities in sodium current and calcium homoeostasis as drivers of arrhythmogenesis in hypertrophic cardiomyopathy.
Acute restraint stress provokes sudden cardiac death in normotensive rats and enhances susceptibility to arrhythmogenic effects of adrenaline in spontaneously hypertensive rats.
An Unusual Case of Syncope in a Young Female with Incidental Long QTc Interval.
Applicability of the AHA/ACC/HRS Guideline for Implantable Cardioverter Defibrillator Implantation in Japanese Patients With Cardiac Sarcoidosis.
Arrhythmic events in Brugada syndrome patients induced by fever.
Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: An Updated Review of Diagnosis and Management.
Arrhythmogenic Right Ventricular Cardiomyopathy: A Review of Living and Deceased Probands.
Arrhythmogenic right ventricular cardiomyopathy: diagnosis and risk stratification.
Arrhythmogenic right ventricular cardiomyopathy: ECG progression over time and correlation with long-term follow-up.
Arrhythmogenic Right Ventricular Cardiomyopathy: Risk Stratification and Indications for Defibrillator Therapy.
Arrhythmogenic right ventricular dysplasia: a United States experience.
Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy.
Atrial fibrillation and risk of major arrhythmic events in Brugada syndrome: A meta-analysis.
Biophysical Characterization of a Novel SCN5A Mutation Associated With an Atypical Phenotype of Atrial and Ventricular Arrhythmias and Sudden Death.
Brief sympathetic activation precedes the development of ventricular tachycardia and ventricular fibrillation in hibernating myocardium.
Brugada disease: chronology of discovery and paternity. Preliminary observations and historical aspects.
Brugada syndrome 2012.
Brugada Syndrome: The Role of Risk Stratification in Selecting Patients for Implantable Cardioverter-defibrillator Placement.
Can sudden cardiac death in the young be predicted and prevented? Lessons from autopsy for the emergency physician.
Cardiac arrest recorded on ambulatory electrocardiograms.
Cardiac arrhythmias and conduction disturbances in autoimmune rheumatic diseases.
Cardiac arrhythmias and sudden death in infancy: implication for the medicolegal investigation.
Cardiac autonomic control in Brugada syndrome patients during sleep: The effects of sleep disordered breathing.
CarDiac MagnEtic Resonance for Primary Prevention Implantable CardioVerter DebrillAtor ThErapy international registry: Design and rationale of the DERIVATE study.
Catecholaminergic polymorphic ventricular tachycardia, an update.
Catheter Ablation of Ventricular Tachycardia in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy.
Catheter ablation to prevent sudden cardiac death.
Clinical significance of new-onset atrial fibrillation in patients with hypertrophic cardiomyopathy.
Current and state of the art on the electrophysiologic characteristics and catheter ablation of arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Current Perspectives on Sudden Cardiac Death in Hemodialysis Patients.
Development of a Novel Risk Prediction Model for Sudden Cardiac Death in Childhood Hypertrophic Cardiomyopathy (HCM Risk-Kids).
Differences in 12-lead electrocardiogram between symptomatic and asymptomatic Brugada syndrome patients.
Early autonomic and repolarization abnormalities contribute to lethal arrhythmias in chronic ischemic heart failure: characteristics of a novel heart failure model in dogs with postmyocardial infarction left ventricular dysfunction.
Effect of dietary n-3 polyunsaturated fatty acids on the inducibility of ventricular tachycardia in patients with ischemic cardiomyopathy.
Elevated B-type natriuretic peptide levels in patients with nonischemic cardiomyopathy predict occurrence of arrhythmic events.
Enhanced American College of Cardiology/American Heart Association Strategy for Prevention of Sudden Cardiac Death in High-Risk Patients With Hypertrophic Cardiomyopathy.
Epidemiology and stratification of risk for sudden cardiac death.
Evidence-based analysis of risk factors for sudden cardiac death.
Exercise-induced quantitative microvolt T-wave alternans in hypertrophic cardiomyopathy.
Frequency of cardiac death in children with idiopathic dilated cardiomyopathy.
Future developments in implantable cardioverter defibrillators: the optimal device.
Genetic and clinical aspects of Brugada syndrome: an update.
Heart Rate Variability Analysis to Predict Onset of Ventricular Tachyarrhythmias in Implantable Cardioverter Defibrillators.
Heart rhythm at the time of death documented by an implantable loop recorder.
Holter monitoring in the prognosis of sudden cardiac death.
Hypertrophic cardiomyopathy: Can the noninvasive diagnostic testing identify high risk patients?
IL-18 mediates sickle cell cardiomyopathy and ventricular arrhythmias.
Impact of clinical and genetic findings on the management of young patients with Brugada syndrome.
Implantable cardioverter defibrillator therapy.
Implantable cardioverter defibrillators: arrhythmias. A rapid and systematic review.
Implantation of the automatic cardioverter-defibrillator.
Implications of multiple late gadolinium enhancement lesions on the frequency of left ventricular reverse remodeling and prognosis in patients with non-ischemic cardiomyopathy.
Improvement in sudden cardiac death risk prediction by the enhanced American College of Cardiology/American Heart Association strategy in Chinese patients with hypertrophic cardiomyopathy.
Inherited Arrhythmia Syndrome Predisposing to Sudden Cardiac Death.
Late gadolinium enhancement location assessed by magnetic resonance and arrhythmogenic risk in hypertrophic cardiomyopathy.
Left intraventricular pressure gradient in hypertrophic cardiomyopathy patients receiving implantable cardioverter-defibrillators for primary prevention.
Long-term follow-up and risk assessment of arrhythmogenic right ventricular dysplasia/cardiomyopathy: personal experience from different primary and tertiary centres.
Long-term prognosis of patients diagnosed with Brugada syndrome: Results from the FINGER Brugada Syndrome Registry.
Magnetic Resonance Imaging Risk Factors for Ventricular Arrhythmias in Tetralogy of Fallot.
Management of arrhythmias in ischemic heart disease. The role of beta blockers.
Mechanism and prediction of sudden cardiac death in arrhythmia patients using electrophysiological studies.
Mechanisms of sudden cardiac death.
Microvolt T wave alternans (MTWA)--a new non-invasive predictor of sudden cardiac death.
Mitral valve prolapse: an underestimated cause of sudden cardiac death-a current review of the literature.
Modulation of QT interval by cardiac sympathetic nerve sprouting and the mechanisms of ventricular arrhythmia in a canine model of sudden cardiac death.
Monogenec Arrhythmic Syndromes: From Molecular and Genetic Aspects to Bedside.
Natural History of Arrhythmogenic Cardiomyopathy.
Nerve sprouting and sudden cardiac death.
New Approaches in the Management of Sudden Cardiac Death in Patients with Heart Failure-Targeting the Sympathetic Nervous System.
Non-arrhythmic causes of sudden death: A comprehensive review.
Non-sustained ventricular tachycardia as a predictor of sudden cardiac death in patients with left ventricular dysfunction: A meta-analysis.
Normokinesia adjacent to left ventricular aneurysm: a differential risk for sudden cardiac death.
Outcome after cardiopulmonary resuscitation in patients with congenital heart disease.
Outcome and complications after implantable cardioverter defibrillator therapy in hypertrophic cardiomyopathy: systematic review and meta-analysis.
Pharmacotherapy in inherited and acquired ventricular arrhythmia in structurally normal adult hearts.
Preclinical short QT syndrome models: studying the phenotype and drug-screening.
Predicting the risk of sudden cardiac death.
Prediction of sudden cardiac death after acute myocardial infarction: role of Holter monitoring in the modern treatment era.
Predictors of right ventricular function and size in patients with hypertrophic cardiomyopathy.
Predictors of Sudden Cardiac Death in Doberman Pinschers with Dilated Cardiomyopathy.
Predictors of sudden cardiac death in hypertrophic cardiomyopathy.
Prevalence of arrhythmia-associated gene mutations and risk of sudden cardiac death in the Finnish population.
Primary and secondary prevention of sudden cardiac death: the role of the implantable cardioverter defibrillator.
Profiling risk from arrhythmic or hemodynamic death.
Prognostic factors affecting the all-cause death and sudden cardiac death rates of post myocardial infarction patients with low left ventricular ejection fraction.
Prognostic Role of Late Gadolinium Enhancement in Patients With Hypertrophic Cardiomyopathy and Low-to-Intermediate Sudden Cardiac Death Risk Score.
Prognostic value of electrocardiographic time intervals and QT rate dependence in hypertrophic cardiomyopathy.
Prognostic value of myocardial fibrosis on cardiac magnetic resonance imaging in patients with ischemic cardiomyopathy: A systematic review.
Prospective risk stratification of sudden cardiac death in Marfan's syndrome.
Proteasome inhibition 1 h following ischemia protects GRK2 and prevents malignant ventricular tachyarrhythmias and SCD in a model of myocardial infarction.
Recent developments in the management of patients at risk for sudden cardiac death.
Relation of 12-lead electrocardiogram patterns to implanted defibrillator-terminated ventricular tachyarrhythmias in hypertrophic cardiomyopathy.
Relation of Late Gadolinium Enhancement and Extracellular Volume Fraction to Ventricular Arrhythmias in Hypertrophic Cardiomyopathy.
Relationship between impaired repolarization parameters and poor cardiovascular clinical outcomes in patients with potentially serious coronary artery anomalies.
Repolarization abnormalities and afterdepolarizations in a canine model of sudden cardiac death.
Review on sudden death risk reduction after septal reduction therapies in hypertrophic obstructive cardiomyopathy.
Ring-like late gadolinium enhancement for predicting ventricular tachyarrhythmias in non-ischaemic dilated cardiomyopathy.
Risk factors for lethal arrhythmic events in children and adolescents with hypertrophic cardiomyopathy and an implantable defibrillator: An international multicenter study.
Risk factors for sudden cardiac death to determine high risk patients in specific patient populations that may benefit from a wearable defibrillator.
Risk Markers and Appropriate Implantable Defibrillator Therapy in Hypertrophic Cardiomyopathy.
Risk stratification for sudden cardiac death after septal myectomy.
Risk stratification for sudden cardiac death in hypertrophic cardiomyopathy: systematic review of clinical risk markers.
Risk Stratification for Sudden Cardiac Death.
Role of antiarrhythmic therapy in patients at risk for sudden cardiac death: an evidence-based review.
Role of drugs and devices in patients at risk of sudden cardiac death.
Role of risk stratification and genetics in sudden cardiac death.
Serum lipid feature and potential biomarkers of lethal ventricular tachyarrhythmia (LVTA) induced by myocardial ion channel diseases: a rat model study.
Sudden cardiac death and the use of implantable cardioverter-defibrillators in pediatric patients. The Pediatric Electrophysiology Society.
Sudden cardiac death in football players: Towards a new pre-participation algorithm.
Sudden Cardiac Death in Ischemic Heart Disease: Pathophysiology and Risk Stratification.
Sudden cardiac death in Long QT syndrome (LQTS), Brugada syndrome, and catecholaminergic polymorphic ventricular tachycardia (CPVT).
Sudden cardiac death in patients with chronic coronary heart disease.
Sudden cardiac death in patients with hypertrophic cardiomyopathy: from bench to bedside with an emphasis on genetic markers.
Sudden cardiac death in young competitive athletes due to genetic cardiac abnormalities.
Sudden Cardiac Death Prediction in Arrhythmogenic Right Ventricular Cardiomyopathy: A Multinational Collaboration.
Sudden cardiac death: implantable cardioverter defibrillators and pharmacological treatments.
Sudden death in cardiac sarcoidosis: an analysis of nationwide clinical and cause-of-death registries.
Sudden death in patients with chronic bifascicular block.
Sudden Death Mechanisms in Non-ischemic Cardiomyopathies; Insights gleaned from clinical implantable cardioverter-defibrillator trials.
Surgical ablation of ventricular tachycardia in patients with repaired tetralogy of Fallot.
T wave alternans and ventricular tachyarrhythmia risk stratification: a review.
T-wave alternans and sudden cardiac death.
Ten advances defining sudden cardiac death.
The amount of late gadolinium enhancement outperforms current guideline-recommended criteria in the identification of patients with hypertrophic cardiomyopathy at risk of sudden cardiac death.
The Application of Ambulatory Electrocardiographically-Based T-Wave Alternans in Patients with Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy.
The clinical challenge of preventing sudden cardiac death immediately after acute ST-elevation myocardial infarction.
The effect of aldosterone antagonists for ventricular arrhythmia: a meta-analysis.
The Midlands Trial of Empirical Amiodarone versus Electrophysiology-guided Interventions and Implantable Cardioverter-defibrillators (MAVERIC): a multi-centre prospective randomised clinical trial on the secondary prevention of sudden cardiac death.
The Postmortem Interpretation of Cardiac Genetic Variants of Unknown Significance in Sudden Death in the Young: A Case Report and Review of the Literature.
The problem of indeterminate microvolt T-wave alternans results in patients with left ventricular dysfunction referred for implantable cardioverter-defibrillator implantation in the primary prevention of sudden cardiac death.
The wearable cardioverter-defibrillator in a real-world clinical setting: experience in 102 consecutive patients.
The wearable cardioverter-defibrillator vest: Indications and ongoing questions.
Usefulness of Electrocardiographic Patterns at Presentation to Predict Long-term Risk of Cardiac Death in Patients With Hypertrophic Cardiomyopathy.
Ventricular arrhythmia and sudden cardiac death in Fabry disease: a systematic review of risk factors in clinical practice.
Ventricular Arrhythmias and Sudden Cardiac Death.
Ventricular arrhythmias in nonischemic cardiomyopathy.
Ventricular tachycardia-inducibility predicts arrhythmic events in post-myocardial infarction patients with low ejection fraction. A systematic review and meta-analysis.
Vital exhaustion and sudden cardiac death in the Atherosclerosis Risk in Communities Study.
Whole-Exome Sequencing Identifies a Novel Mutation (p.L320R) of Alpha-Actinin 2 in a Chinese Family with Dilated Cardiomyopathy and Ventricular Tachycardia.
[Automatic external defibrillator--mode of operation and clinical use]
[Heart Rate Turbulence and T-Wave Alternans as Markers of Risk of Sudden Cardiac Death in Patients With Hypertrophic Cardiomyopathy.]
[Implantable cardioverter-defibrillator in patients with chronic heart failure]
[Limits and scopes of invasive risk stratification. Do we still need programmed ventricular stimulation?]
[Non-pharmacologic prevention of sudden cardiac death]
[Primary prevention of sudden cardiac death implanted cardioverter defibrillator (ICD) versus antiarrhythmic drugs]
[Sudden cardiac death : Epidemiology, pathophysiology and risk stratification].
[Sudden cardiac death and automated external defibrillators. Where we are in 2012?].
[Sudden Cardiac Death in Patients With Hypertrophic Cardiomyopathy].
[The ICD as primary prevention. Rare indications]
[Ventricular arrhythmias and sudden cardiac death in acute myocardial infarct in the era of thrombolytics]
[Ventricular tachycardia : Treatment and prognostic significance].
[Wearable cardioverter-defibrillators: clinical experience and future perspectives].
[Worldwide experience with automated external defibrillators : What have we achieved? What else can we expect?].
Tachypnea
Which Febrile Children with Sickle Cell Disease Need a Chest X-Ray?
Tauopathies
Spinocerebellar degeneration: Discrepancies between clinical and pathological diagnoses.
Teratoma
Erythropoietic differentiation of a human embryonic stem cell line harbouring the sickle cell anaemia mutation.
Shadow cell differentiation in testicular teratomas. A report of two cases.
Shadow Cell Differentiation: A Comparative Analysis of Modes of Cell Death with Apoptosis and Epidermal/Trichilemmal Keratinization.
Tetanus
Lymphocyte blastogenic responses in sickle cell disease.
Tetralogy of Fallot
Spondylocostal dysostosis with tetralogy of Fallot and herniation of the spleen through the diaphragm.
Sudden cardiac death in adults with congenital heart disease: does QRS-complex fragmentation discriminate in structurally abnormal hearts?
Thalassemia
A novel tandem mass spectrometry method for first-line screening of mainly beta-thalassemia from dried blood spots.
A systematic review of quality of life in sickle cell disease and thalassemia after stem cell transplant or gene therapy.
Adherence to iron chelation therapy and associated healthcare resource utilization and costs in Medicaid patients with sickle cell disease and thalassemia.
Administrative data sets and health services research on hemoglobinopathies: a review of the literature.
Allogeneic cellular gene therapy for hemoglobinopathies.
Ambulatory hypertension in a pediatric cohort of sickle cell disease.
Analysis of hippocampal subfields in sickle cell disease using ultrahigh field MRI.
Availability of unrelated donors for hematopoietic stem cell transplantation for hemoglobinopathies.
CAREST-Multilingual Regional Integration for Health Promotion and Research on Sickle Cell Disease and Thalassemia.
Cell and Gene Therapy for Anemia: Hematopoietic Stem Cells and Gene Editing.
Children with HbS?0 thalassemia have higher hemoglobin levels and lower incidence rate of acute chest syndrome compared to children with HbSS.
Chronic Pulmonary Complications of Sickle Cell Disease.
Clinical Features of ?-Thalassemia and Sickle Cell Disease.
Clinical phenotypes and outcomes of precapillary pulmonary hypertension of sickle cell disease.
Clinical studies with fetal hemoglobin-enhancing agents in sickle cell disease.
Clinical variability and molecular characterization of Hbs/G? (A???)0-thal and Hbs/HPFH in Indian sickle cell disease patients: AIIMS experience.
Decision making for hematopoietic stem cell transplantation in pediatric, adolescent, and young adult patients with a hemoglobinopathy-Shared or not?
Decreased Bleeding Incidence with Direct Oral Anticoagulants Compared to Vitamin K Antagonist and Low-Molecular-Weight Heparin in Patients with Sickle Cell Disease and Venous Thromboembolism.
Development of interactive algorithm for clinical management of acute events related to sickle cell disease in emergency department.
Disparity in the management of iron overload between patients with sickle cell disease and thalassemia who received transfusions.
Drawings of Blood Cells Reveal People's Perception of Their Blood Disorder: A Pilot Study.
Effect of Poloxamer 188 vs Placebo on Painful Vaso-Occlusive Episodes in Children and Adults With Sickle Cell Disease: A Randomized Clinical Trial.
Gene therapy for hemoglobinopathies: progress and challenges.
Genetic modulators of sickle cell disease in French Guiana: Markers of the slave trade.
Genetic variants at HbF-modifier loci moderate anemia and leukocytosis in sickle cell disease in Tanzania.
Growth differentiation factor-15 in young sickle cell disease patients: relation to hemolysis, iron overload and vascular complications.
Hemoglobinopathies and Stroke: Strategies for Prevention and Treatment.
How do I incorporate red cell genotyping to improve chronic transfusion therapy?
Hydroxyurea therapy in children severely affected with sickle cell disease.
Identification of patients with hemoglobin SS/S?0 thalassemia disease and pain crises within electronic health records.
Increased Level of Factor VIII and Physiological Inhibitors of Coagulation in Patients with Sickle Cell Disease.
Infections in thalassemia and hemoglobinopathies: focus on therapy-related complications.
Inhibition of ?/? Globin Gene Switching in CD 34+?Derived Erythroid Cells by BCL11A RNA Silencing.
Iron metabolism and iron chelation in sickle cell disease.
Left Ventricular Structural and Functional Changes in Children With ?-Thalassemia and Sickle Cell Disease: Relationship to Sleep-disordered Breathing.
Management of Sickle Cell Disease in Children.
Mechanisms of vasculopathy in sickle cell disease and thalassemia.
Monitoring retinal pathology and cerebral injury in sickle cell disease using spectral-domain optical coherence tomography in pediatric patients.
National registry of hemoglobinopathies in Spain (REPHem).
Natural Inhibitors and Lipids in Patients with Sickle Cell Disease.
New variants in beta globin gene among the Palestinian refugees with sickle cell disease in Lebanon.
Nitric oxide and arginine dysregulation: a novel pathway to pulmonary hypertension in hemolytic disorders.
Non Transferrin Bound Labile Plasma Iron and Iron Overload in Sickle Cell Disease: a comparative study between Sickle Cell Disease and beta Thalassemic patients.
Ocular manifestations in egyptian children and young adults with sickle cell disease.
Ototoxicity in hemoglobinopathy patients chelated with desferrioxamine.
Outcomes, utilization, and costs among thalassemia and sickle cell disease patients receiving deferoxamine therapy in the United States.
Pediatric hemoglobinopathies: from the bench to the bedside.
Posterior Reversible Encephalopathy Syndrome after Hematopoietic Cell Transplantation in Children with Hemoglobinopathies.
Predictors and Correlates of Fatigue in Sickle Cell Disease Patients.
Prophylactic penicillin after 5 years of age in patients with sickle cell disease: A survey of sickle cell disease experts.
Recent advances in bone marrow transplantation in hemoglobinopathies.
Related umbilical cord blood transplantation in patients with thalassemia and sickle cell disease.
Sample suitability for the detection of minor white cell populations (microchimerism) by polymerase chain reaction.
Serum ferritin underestimates liver iron concentration in transfusion independent thalassemia patients as compared to regularly transfused thalassemia and sickle cell patients.
Serum zinc levels and zinc binding capacity in thalassemia.
Sickle cell disease and stroke.
Sickle cell disease in Germany: Results from a national registry.
Splenectomy and acute splenic sequestration crises in sickle cell disease.
Successful matched sibling donor marrow transplantation following reduced intensity conditioning in children with hemoglobinopathies.
Survey of sickle cell disease in Italy.
Thalassemia major and sickle cell disease in adolescents and young adults.
The clinical impact of glucose-6-phosphate dehydrogenase deficiency in patients with sickle cell disease.
The diagnosis and management of hemoglobinopathies during pregnancy.
The Effect of Hydroxyurea Therapy in Bahraini Sickle Cell Disease Patients.
Thrombophilic mutations among Southern Iranian patients with sickle cell disease: high prevalence of factor V Leiden.
Transcranial color Doppler in stroke-free adult patients with sickle cell disease.
Transfusion service knowledge and immunohaematological practices related to sickle cell disease and thalassemia.
Umbilical Cord Blood Transplantation for Children with Thalassemia and Sickle Cell Disease.
Updated Worldwide Epidemiology of Inherited Erythrocyte Disorders.
Urinary Transforming Growth Factor ?-1 as a Marker of Renal Dysfunction in Sickle Cell Disease.
[Progress in Gene Therapy of Sickle Cell Disease Based on Hemoglobin F--Review].
[The use of hydroxyurea in severe forms of sickle cell disease: study of 47 Tunisian paediatric cases]
Thrombocytosis
Severity of Anaemia Has Corresponding Effects on Coagulation Parameters of Sickle Cell Disease Patients.
Thromboembolism
Clinical, laboratory, and genetic risk factors for thrombosis in sickle cell disease.
Gangrene of the digits of the right lower limb in a patient with homozygous sickle cell disease and ulcerative colitis.
Hypertrophic cardiomyopathy with a large apical ventricular aneurysm and mural thrombus.
Increased Level of Factor VIII and Physiological Inhibitors of Coagulation in Patients with Sickle Cell Disease.
Left Ventricular Non-Compaction in Athletes: To Play or Not to Play.
Megestrol Acetate Induced Paradoxical Embolism in a Sickle Cell Disease Patient.
Outcome of Pregnancy in Saudi Women with Sickle Cell Disease Attending the Tertiary Care University Hospital in Eastern Province of Saudi Arabia.
Prognostic role of left ventricular apical aneurysm in hypertrophic cardiomyopathy: A systematic review and meta-analysis.
Successful pulmonary thromboendarterectomy in a patient with sickle cell disease and associated resolution of a leg ulcer.
The different facets of sickle cell disease-related pulmonary hypertension.
The possible role of reticulocytes in sickle cell disease associated thromboembolism.
Thromboinflammation
Complement Component C5 and TLR Molecule CD14 Mediate Heme-Induced Thromboinflammation in Human Blood.
Targeting the AnxA1/Fpr2/ALX pathway regulates neutrophil function, promoting thromboinflammation resolution in sickle cell disease.
Thrombophilia
ADAMTS-13-VWF axis in sickle cell disease patients.
Clinical biomarkers in sickle cell disease.
Effect of Chronic Blood Transfusion on Biomarkers of Coagulation Activation and Thrombin Generation in Sickle Cell Patients at Risk for Stroke.
Factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations among patients with sickle cell disease in Eastern Saudi Arabia.
Gangrene of the digits of the right lower limb in a patient with homozygous sickle cell disease and ulcerative colitis.
Hemoglobinopathies and Stroke: Strategies for Prevention and Treatment.
Hypercoagulability in sickle cell disease: new approaches to an old problem.
Intracranial aneurysms in sickle cell disease: Aneurysms characteristics and modalities of endovascular approach to treat these patients.
Intracranial stenting as monotherapy in subarachnoid hemorrhage and sickle cell disease.
Pathways to pulmonary hypertension in sickle cell disease: the search for prevention and early intervention.
Platelets, coagulation, and fibrinolysis in sickle cell disease: their possible role in vascular occlusion.
Prothrombin mutant, factor V Leiden, and thermolabile variant of methylenetetrahydrofolate reductase among patients with sickle cell disease in Brazil.
Red blood cells and thrombin generation in sickle cell disease.
Sickle cell disease is associated with iron mediated hypercoagulability.
The acceleration of the propagation phase of thrombin generation in patients with steady-state sickle cell disease is associated with circulating erythrocyte-derived microparticles.
Thrombin generation in vivo and ex vivo in sickle cell disease patients.
Thrombosis and sickle cell disease.
Venous Thromboembolism in Children with Sickle Cell Disease: A Retrospective Cohort Study.
Thrombophlebitis
Elevated circulating endothelial membrane microparticles in paroxysmal nocturnal haemoglobinuria.
Thrombosis
A novel inflammatory role for platelets in sickle cell disease.
Analysis of the operation of the SCD Response intermittent compression system.
Association between apolipoprotein epsilon4 allele, factor V Leiden, and plasma lipid and lipoprotein levels with sickle cell disease in southern Iran.
Biomarkers of inflammation, growth factor, and coagulation activation in patients with sickle cell disease.
Blockade of placental growth factor reduces vaso-occlusive complications in murine models of sickle cell disease.
Central venous catheter complications in sickle cell disease.
Circulating platelet and erythrocyte microparticles in young children and adolescents with sickle cell disease: Relation to cardiovascular complications.
Clinical, laboratory, and genetic risk factors for thrombosis in sickle cell disease.
Congestive heart failure and Virchow's triad: a neglected association.
Coronary atherosclerosis in unheralded sudden coronary death under age 50: histo-pathologic comparison with 'healthy' subjects dying out of hospital.
Deep venous thrombosis and pulmonary embolism in hospitalized patients with sickle cell disease.
Diet and medication for heart protection in secondary prevention of coronary heart disease. New concepts.
Discrete event simulation model of sudden cardiac death predicts high impact of preventive interventions.
Elevated circulating endothelial membrane microparticles in paroxysmal nocturnal haemoglobinuria.
Factor V Leiden G1691A and prothrombin G20210A mutations among Palestinian patients with sickle cell disease.
Gastrointestinal pathology in sickle cell disease.
How we diagnose and treat venous thromboembolism in sickle cell disease.
In-hospital Outcomes and Characteristics of Heart Failure in Sickle Cell Disease.
Laparoscopic splenic procedures in children: experience in 231 children.
Large-vessel occlusion in sickle cell disease: pathogenesis, clinical consequences, and therapeutic implications.
Liver transplantation in children with sickle-cell disease.
Long-term central venous access in patients with sickle cell disease. Incidence of thrombotic and infectious complications.
Mitochondrial reactive oxygen species scavenging attenuates thrombus formation in a murine model of sickle cell disease.
Morbidity associated with sickle cell disease in pregnancy.
Morphological and functional platelet abnormalities in Berkeley sickle cell mice.
NLRP3 inflammasome and bruton tyrosine kinase inhibition interferes with upregulated platelet aggregation and in vitro thrombus formation in sickle cell mice.
Paradoxical protection from atherosclerosis and thrombosis in a mouse model of sickle cell disease.
Pathologically stiff erythrocytes impede contraction of blood clots.
Pathophysiology of coronary artery disease leading to acute coronary syndromes.
Plasminogen activator inhibitor-1 (PAI-1) 4G/5G polymorphism, coronary thrombosis, and myocardial infarction in middle-aged Finnish men who died suddenly.
Platelet activation in patients with sickle disease, hemolysis-associated pulmonary hypertension, and nitric oxide scavenging by cell-free hemoglobin.
Platelets, coagulation, and fibrinolysis in sickle cell disease: their possible role in vascular occlusion.
Polymorphism in exon 10 of the human coagulation factor V gene in a population at risk for sickle cell disease.
Pregnancy in patients with sickle cell disease: maternal and perinatal outcomes.
Prevalence of intracardiac shunting in children with sickle cell disease and stroke.
Prevention of venous thromboembolism in trauma patients.
Prothrombin mutant, factor V Leiden, and thermolabile variant of methylenetetrahydrofolate reductase among patients with sickle cell disease in Brazil.
Pulmonary Embolism in Sickle Cell Disease: A Case-Control Study.
Pulmonary hypertension in sickle cell disease.
Red blood cells modulate structure and dynamics of venous clot formation in sickle cell disease.
Risk factor profile for sudden cardiac death during mountain hiking.
Sickle cell disease in pregnancy: maternal complications in a medicaid-enrolled population.
Sickle cell disease, sickle trait and the risk for venous thromboembolism: a systematic review and meta-analysis.
Sickle Cell Disease: A Paradigm for Venous Thrombosis Pathophysiology.
Sickle cell disease: current activities, public health implications, and future directions.
Spinocerebellar degeneration: Discrepancies between clinical and pathological diagnoses.
Subacute combined degeneration of the spinal cord concurrent with acute pulmonary embolism: a case report.
Sudden Cardiac Death in Anabolic-Androgenic Steroid Users: A Literature Review.
Targeting AnxA1/Formyl Peptide Receptor 2 Pathway Affords Protection against Pathological Thrombo-Inflammation.
The possible role of reticulocytes in sickle cell disease associated thromboembolism.
The relevance of platelet and fibrin thromboembolism of the coronary microcirculation, with special reference to sudden cardiac death.
The utility of thromboelastography and thrombin generation in assessing the prothrombotic state of adults with sickle cell disease.
Thrombus composition in sudden cardiac death from acute myocardial infarction.
Thyroid Function 'in Egyptian Children with Sickle Cell Anemia in correlation with iron' load.
Totally implantable intravenous catheters in the management of sickle cell anemia.
Venous thromboembolism in adults with sickle cell disease: experience of a single centre in the UK.
Venous thromboembolism incidence in the Cooperative Study of Sickle Cell Disease.
Thrombotic Microangiopathies
Atypical presentation of acute post-infectious glomerulonephritis in patients with sickle cell disease: report of two cases.
Thymoma
Mediastinal tumor resection in a patient with spinocerebellar degeneration.
Thyroid Cancer, Papillary
Histone methyltransferase KMT5A gene modulates oncogenesis and lipid metabolism of papillary thyroid cancer in vitro.
Thyroid Carcinoma, Anaplastic
Aberrant lipid metabolism in anaplastic thyroid carcinoma reveals stearoyl CoA desaturase 1 as a novel therapeutic target.
Exosome-mediated delivery of SCD-1 siRNA promoted the death of anaplastic thyroid carcinoma cells via regulating ROS level.
Thyroiditis, Autoimmune
Subacute combined degeneration of the spinal cord with concomitant autoimmune disease: report of 2 cases.
Tics
Stearoyl-CoA Desaturase Promotes Liver Fibrosis and Tumor Development in Mice via a Wnt Positive-Signaling Loop by Stabilization of Low-Density Lipoprotein-Receptor-Related Proteins 5 and 6.
Totally implantable intravenous catheters in the management of sickle cell anemia.
Tinnitus
Superior canal dehiscence plugging reduces dizziness handicap.
Underwater Endoscopic Repair of Superior Canal Dehiscence.
Toothache
Sickle cell disorder and orofacial pain in Jamaican patients.
Torsades de Pointes
A review of ECG and QT interval measurement use in a public psychiatric inpatient setting.
Cardiovascular safety of antipsychotics: a clinical overview.
Effect of GWAS-Identified Genetic Variants on Maximum QT Interval in Patients With Schizophrenia Receiving Antipsychotic Agents: A 24-Hour Holter ECG Study.
Pharmacotherapy in inherited and acquired ventricular arrhythmia in structurally normal adult hearts.
[Long and short QT syndromes : Emergency treatment and secondary prophylaxis].
Toxoplasmosis
Sterculic Acid and Its Analogues Are Potent Inhibitors of Toxoplasma gondii.
Transfusion Reaction
A case of delayed hemolytic transfusion reaction in sickle cell disease patient.
Challenges in preventing and treating hemolytic complications associated with red blood cell transfusion.
Clinical presentation of delayed hemolytic transfusion reactions and hyperhemolysis in sickle cell disease.
Complement activation during intravascular hemolysis: Implication for sickle cell disease and hemolytic transfusion reactions.
Delayed hemolytic transfusion reaction/hyperhemolysis syndrome in children with sickle cell disease.
Fatal Delayed Haemolytic Transfusion Reaction and Hyperhaemolysis Syndrome in a Pregnant Woman with Sickle Cell Anaemia.
Immunohematologic tolerance of chronic transfusion exchanges with erythrocytapheresis in sickle cell disease.
Immunoregulatory networks in sickle cell alloimmunization.
Multiple hemolytic transfusion reactions misinterpreted as severe vaso-occlusive crisis in a patient with sickle cell disease.
Prevalence and risk factors for red blood cell alloimmunisation among sickle cell patients in Mwanza City, Tanzania.
Principles and problems of transfusion in sickle cell disease.
Red blood cell alloimmunization and delayed hemolytic transfusion reactions in patients with sickle cell disease.
Rituximab for prevention of delayed hemolytic transfusion reaction in sickle cell disease.
The cause and pathogenesis of hemolytic transfusion reactions in sickle-cell disease.
Treatment with intravenous immunoglobulin and steroids may correct severe anemia in hyperhemolytic transfusion reactions: case report and literature review.
Two Consecutive Episodes of Severe Delayed Hemolytic Transfusion Reaction in a Sickle Cell Disease Patient.
Trauma, Nervous System
Sickle cell disease.
Tremor
Bartonella henselae Infection in Sickle Cell Disease Mice Is Associated with Hyperalgesia.
Thalamic stimulation for disabling tremor in a patient with spinocerebellar degeneration.
[Antidotal effects of 2,3-dimercaptopropane-1-sulfonate sodium (DMPS) and combined with diazepam on acute poisoning caused by sodium ammonium dimethyl-2-propano-1,3-dithiosulfate monohydrate (SCD)]
Tricuspid Valve Insufficiency
A Sickle Cell Disease Patient with Severe Tricuspid Regurgitation and Early Developed Pulmonary Hypertension.
Cardiac Structural and Functional Changes Evaluated by Transthoracic and Tissue Doppler Echocardiography in Adult Patients with Sickle Cell Disease.
Clinical management of adult sickle-cell disease.
Echocardiographic parameters to identify sickle cell patients with cardio-pathology.
Left ventricular remodeling in patients with sickle cell disease: determinants factors and impact on outcome.
Perioperative Endocarditis Management in a Patient with Homozygous Sickle Cell Disease.
Predictors of ventricular tachyarrhythmia occurring late after intracardiac repair of tetralogy of Fallot: combination of QRS duration change rate and tricuspid regurgitation pressure gradient.
Ventricular Structure and Function in Children With Sickle Cell Disease Using Conventional and Tissue Doppler Echocardiography.
Tuberculosis
Complete auxotrophy for unsaturated fatty acids requires deletion of two sets of genes in Mycobacterium smegmatis.
Flux balance analysis of mycolic Acid pathway: targets for anti-tubercular drugs.
Identification of Rv3230c as the NADPH oxidoreductase of a two-protein DesA3 acyl-CoA desaturase in Mycobacterium tuberculosis H37Rv.
In vivo inactivation of the mycobacterial integral membrane stearoyl coenzyme A desaturase DesA3 by a C-terminus-specific degradation process.
Tuberculosis in adult patients with sickle cell disease.
Unique mechanism of action of the thiourea drug isoxyl on Mycobacterium tuberculosis.
Tuberculosis, Cutaneous
Incidence of cutaneous tuberculosis in patients with organ tuberculosis.
Tuberculosis, Lymph Node
Tuberculosis in adult patients with sickle cell disease.
Tyrosinemias
Differential diagnosis of Schnyder corneal dystrophy.
Uremia
[Sudden cardiac death in diabetes mellitus].
Urinary Bladder Neoplasms
FGFR3 stimulates stearoyl CoA desaturase 1 activity to promote bladder tumor growth.
Increased expression of the gene encoding stearoyl-CoA desaturase 1 in human bladder cancer.
Inhibition of stearoyl CoA desaturase-1 activity suppresses tumour progression and improves prognosis in human bladder cancer.
Urinary Bladder, Overactive
Dysregulated NO/PDE5 signaling in the sickle cell mouse lower urinary tract: Reversal by oral nitrate therapy.
Urinary Incontinence
Subacute combined degeneration without nutritional anemia.
Urinary Tract Infections
Abdominal pain in children with sickle cell disease.
Dual kidney transplants from very old or very young donors: long-term outcomes and complications.
Multiple bone and joint diseases in a nigerian sickle cell anaemia: a case report.
Systemic T Cell Subsets and Cytokines in Patients With Homozygous Sickle Cell Disease and Asymptomatic Urinary Tract Infections in Togo.
Urolithiasis
Spontaneous expulsion of large vesicle calculi in a woman with paraparesis.
Usher Syndromes
CDH23 Related Hearing Loss: A New Genetic Risk Factor for Semicircular Canal Dehiscence?
Uterine Hemorrhage
Common gynecological challenges in adolescents with sickle cell disease.
Varicocele
Multiple determinations of sperm DNA fragmentation show that varicocelectomy is not indicated for infertile patients with subclinical varicocele.
Simple determination of human sperm DNA fragmentation with an improved sperm chromatin dispersion test.
Varicose Ulcer
Immediate hemodynamic effect of the additional use of the SCD EXPRESS Compression System in patients with venous ulcers treated with the four-layer compression bandaging system.
Vasculopathy, inflammation, and blood flow in leg ulcers of patients with sickle cell anemia.
Varicose Veins
Improved hemodynamic effectiveness and associated clinical correlations of a new intermittent pneumatic compression system in patients with chronic venous insufficiency.
Vascular Calcification
Calcium and Sudden Cardiac Death in End-Stage Renal Disease.
GPAT4-Generated Saturated LPAs Induce Lipotoxicity through Inhibition of Autophagy by Abnormal Formation of Omegasomes.
Saturated phosphatidic acids mediate saturated fatty acid-induced vascular calcification and lipotoxicity.
Sudden cardiac death in haemodialysis patients: preventative options.
Vascular Diseases
Encephaloduroarteriosynangiosis and encephalomyoarteriosynangiosis for treatment of moyamoya syndrome in pediatric patients with sickle cell disease.
Heme changes HIF-?, eNOS and nitrite production in HUVECs after simvastatin, HU, and ascorbic acid therapies.
Homocysteine in sickle cell disease: relationship to stroke.
Homocysteine is associated with severity of microvasculopathy in sickle cell disease patients.
Paediatric sickle cell disease: pulmonary hypertension but normal vascular resistance.
Prevention of ventricular fibrillation, acute myocardial infarction (myocardial necrosis), heart failure, and mortality by bretylium: is ischemic heart disease primarily adrenergic cardiovascular disease?
Updating the lipids hypothesis of inflammation and vascular disease in patients with chronic kidney disease: a stearoyl-CoA desaturase affair?
Vasculopathy in Sickle Cell Disease: From Red Blood Cell Sickling to Vascular Dysfunction.
Vascular System Injuries
Pathophysiology of stroke in sickle cell disease.
Posterior Sternoclavicular Dislocation: Do We Need "Cardiothoracic Backup"? Insights From a National Sample.
Recurrent large volume silent strokes in sickle cell disease.
Sickle cell disease: current treatment and emerging therapies.
Vasculitis
Sudden cardiac death caused by coronary vasculitis.
Venous Insufficiency
Improved hemodynamic effectiveness and associated clinical correlations of a new intermittent pneumatic compression system in patients with chronic venous insufficiency.
Venous Thromboembolism
A prospective evaluation of standard versus battery-powered sequential compression devices in postsurgical patients.
American Society of Hematology 2019 guidelines for sickle cell disease: cardiopulmonary and kidney disease.
Effectiveness and safety of oral anticoagulants in patients with sickle cell disease and venous thromboembolism: a retrospective cohort study.
Markers of platelet activation, thrombin generation and fibrinolysis in women with sickle cell disease: effects of differing forms of hormonal contraception.
Overcoming challenges of venous thromboembolism in sickle cell disease treatment.
Pulmonary complications of sickle cell disease: a narrative clinical review.
Red blood cells modulate structure and dynamics of venous clot formation in sickle cell disease.
Sickle cell disease and pregnancy outcomes: population-based study on 8.8 million births.
The molecular basis for the prothrombotic state in sickle cell disease.
Thromboinflammatory mechanisms in sickle cell disease - challenging the hemostatic balance.
Two mechanical devices for prophylaxis of thromboembolism after total knee arthroplasty. A prospective, randomised study.
Venous thromboembolism in pregnant women with sickle cell disease: a retrospective database analysis.
Venous thromboembolism incidence in the Cooperative Study of Sickle Cell Disease.
Venous Thromboembolism Prophylaxis in Orthopaedic Trauma Patients: A Survey of OTA Member Practice Patterns and OTA Expert Panel Recommendations.
Venous Thrombosis
Analysis of the operation of the SCD Response intermittent compression system.
Deep venous thrombosis and pulmonary embolism in hospitalized patients with sickle cell disease.
Factor V Leiden G1691A and prothrombin G20210A mutations among Palestinian patients with sickle cell disease.
In-hospital Outcomes and Characteristics of Heart Failure in Sickle Cell Disease.
Morbidity associated with sickle cell disease in pregnancy.
Pregnancy in patients with sickle cell disease: maternal and perinatal outcomes.
Prevention of venous thromboembolism in trauma patients.
Sickle cell disease in pregnancy: maternal complications in a medicaid-enrolled population.
Sickle cell disease, sickle trait and the risk for venous thromboembolism: a systematic review and meta-analysis.
Sickle cell disease: a multigenic perspective of a single-gene disorder.
The molecular basis for the prothrombotic state in sickle cell disease.
Thromboembolic complications following radical retropubic prostatectomy. Influence of external sequential pneumatic compression devices.
Totally implantable intravenous catheters in the management of sickle cell anemia.
Use of Pleuroperitoneal Shunt in Chylothorax Related to Central Line Associated Thrombosis in Sickle Cell Disease.
Venous thromboembolism incidence in the Cooperative Study of Sickle Cell Disease.
Venous Thromboembolism Prophylaxis in Orthopaedic Trauma Patients: A Survey of OTA Member Practice Patterns and OTA Expert Panel Recommendations.
Ventricular Dysfunction
Abnormal myocardial flow reserve in sickle cell disease: a myocardial contrast echocardiography study.
Assessment of ventricular function in adults with sickle cell disease: role of two-dimensional speckle-tracking strain.
Echocardiographic Screening of Cardiovascular Status in Pediatric Sickle Cell Disease.
Left Ventricular Non-Compaction in Athletes: To Play or Not to Play.
Phenotypic expression is a prerequisite for malignant arrhythmic events and sudden cardiac death in arrhythmogenic right ventricular cardiomyopathy.
Primary and secondary prevention of sudden cardiac death: the role of the implantable cardioverter defibrillator.
Sudden Cardiac Death in Adult Congenital Heart Disease.
Sudden cardiac death in adult congenital heart disease: can the unpredictable be foreseen?
Sudden death related cardiomyopathies - Arrhythmogenic right ventricular cardiomyopathy, arrhythmogenic cardiomyopathy, and exercise-induced cardiomyopathy.
Ventricular Dysfunction, Left
Ambulatory ECG-based T-wave alternans predicts sudden cardiac death in high-risk post-MI patients with left ventricular dysfunction in the EPHESUS study.
Current Perspectives on Sudden Cardiac Death in Hemodialysis Patients.
Differential expression of B-type natriuretic peptide between left and right ventricles, with particular regard to sudden cardiac death.
Early autonomic and repolarization abnormalities contribute to lethal arrhythmias in chronic ischemic heart failure: characteristics of a novel heart failure model in dogs with postmyocardial infarction left ventricular dysfunction.
Expanding the phenotype of sudden cardiac death-An unusual presentation of a family with a Lamin A/C mutation.
Experts of the Heart Rhythm Section of the Polish Cardiac Society: opinion on the use of wearable cardioverter-defibrillators in Poland.
Implantable cardioverter defibrillators in patients with valvular cardiomyopathy.
Implantable device therapy.
Long-term follow-up and risk assessment of arrhythmogenic right ventricular dysplasia/cardiomyopathy: personal experience from different primary and tertiary centres.
Mortality and appropriate and inappropriate therapy in patients with ischaemic heart disease and implanted cardioverter-defibrillators for primary prevention: data from the Danish ICD Register.
Predictive Value of Beat-to-Beat QT Variability Index Across the Continuum of Left Ventricular Dysfunction: Competing Risks of Noncardiac or Cardiovascular Death and Sudden or Nonsudden Cardiac Death.
Predictors of sudden cardiac death in high-risk patients following a myocardial infarction.
Primary prevention of defibrillator implantation after myocardial infarction: clinical practice and compliance to guidelines.
Profiling risk from arrhythmic or hemodynamic death.
Relation of body mass index to sudden cardiac death and the benefit of implantable cardioverter-defibrillator in patients with left ventricular dysfunction after healing of myocardial infarction.
Risk factors for sudden cardiac death in patients with chronic renal insufficiency and left ventricular dysfunction.
Risk stratification and primary prevention of sudden cardiac death: sudden death prevention.
Role of drugs and devices in patients at risk of sudden cardiac death.
Sudden cardiac death and heart failure.
Sudden cardiac death in cardiac transplant recipients.
Sudden cardiac death in patients with chronic coronary heart disease.
Sudden Cardiac Death: Lessons Learned from Cardiac Implantable Rhythm Devices.
The problem of indeterminate microvolt T-wave alternans results in patients with left ventricular dysfunction referred for implantable cardioverter-defibrillator implantation in the primary prevention of sudden cardiac death.
The role of antiarrhythmic drug therapy for the prevention of sudden cardiac death.
[Relationship between arrhythmia profile, left ventricular function and sudden death in the post-infarct period of patients resuscitated from heart arrest]
[Wearable cardioverter-defibrillators: clinical experience and future perspectives].
Ventricular Dysfunction, Right
Differential expression of B-type natriuretic peptide between left and right ventricles, with particular regard to sudden cardiac death.
Hemopexin dosing improves cardiopulmonary dysfunction in murine sickle cell disease.
Myocardial ischemia and right ventricular dysfunction in adult patients with sickle cell disease.
Surgical ablation of ventricular tachycardia in patients with repaired tetralogy of Fallot.
Ventricular Fibrillation
A Common Missense Variant in the Neuregulin1 Gene is associated with Both Schizophrenia and Sudden Cardiac Death.
A novel cardiac ryanodine receptor gene (RyR2) mutation in an athlete with aborted sudden cardiac death: a case of adult-onset catecholaminergic polymorphic ventricular tachycardia.
A novel mutation of dipeptidyl aminopeptidase-like protein-6 in a family with suspicious idiopathic ventricular fibrillation.
Abnormalities in sodium current and calcium homoeostasis as drivers of arrhythmogenesis in hypertrophic cardiomyopathy.
Acute restraint stress provokes sudden cardiac death in normotensive rats and enhances susceptibility to arrhythmogenic effects of adrenaline in spontaneously hypertensive rats.
Applicability of the AHA/ACC/HRS Guideline for Implantable Cardioverter Defibrillator Implantation in Japanese Patients With Cardiac Sarcoidosis.
Arrhythmias and sudden cardiac death in post-cardiac transplant patients.
Arrhythmic events in Brugada syndrome patients induced by fever.
Brugada syndrome 2012.
Can sudden cardiac death in the young be predicted and prevented? Lessons from autopsy for the emergency physician.
Catheter Ablation of Ventricular Tachycardia in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy.
Catheter ablation to prevent sudden cardiac death.
Continuous telemetry from a chronic canine model of sudden cardiac death.
Coronary spasm during cardiac electrophysiological study following isoproterenol infusion.
Current and state of the art on the electrophysiologic characteristics and catheter ablation of arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Defibrillation for Ventricular Fibrillation: A Shocking Update.
Early repolarization is associated with a significantly increased risk of ventricular arrhythmias and sudden cardiac death in patients with structural heart diseases.
Efficacy of cardiac resynchronization therapy in very old patients: the Insync/Insync ICD Italian Registry.
Electrocardiogram as a screening tool in the general population: A strategic review.
Enhanced American College of Cardiology/American Heart Association Strategy for Prevention of Sudden Cardiac Death in High-Risk Patients With Hypertrophic Cardiomyopathy.
Epidemiology and genetics of ventricular fibrillation during acute myocardial infarction.
Epidemiology and stratification of risk for sudden cardiac death.
Evaluation of patients with complex ventricular arrhythmias: current noninvasive and invasive methods.
Event and sideline management of sudden cardiac death.
Genetic and clinical aspects of Brugada syndrome: an update.
Genetic predisposition to sudden cardiac death.
Genetics of sudden cardiac death syndromes.
High prevalence of early repolarization in the paediatric relatives of sudden arrhythmic death syndrome victims and in normal controls.
Impact of different selection policies on subcutaneous ICD implants and therapies.
Implantable cardioverter-defibrillators in children.
Implications of multiple late gadolinium enhancement lesions on the frequency of left ventricular reverse remodeling and prognosis in patients with non-ischemic cardiomyopathy.
Late gadolinium enhancement location assessed by magnetic resonance and arrhythmogenic risk in hypertrophic cardiomyopathy.
Long-term follow-up of survivors of prehospital sudden coronary death.
Long-term outcomes in hypertrophic cardiomyopathy caused by mutations in the cardiac troponin T gene.
Mechanisms of sudden cardiac death.
Microvolt T-wave alternans and autonomic nervous system parameters can be helpful in the identification of low-arrhythmic risk patients with ischemic left ventricular systolic dysfunction.
Microvolt T-wave alternans as a predictor of ventricular tachyarrhythmias: a prospective study using atrial pacing.
Modulation of QT interval by cardiac sympathetic nerve sprouting and the mechanisms of ventricular arrhythmia in a canine model of sudden cardiac death.
Monogenec Arrhythmic Syndromes: From Molecular and Genetic Aspects to Bedside.
Natural History of Arrhythmogenic Cardiomyopathy.
Nerve sprouting and sudden cardiac death.
Non-arrhythmic causes of sudden death: A comprehensive review.
Overview of completed sudden death trials: European experience.
Pathology of the myocardium and the conduction system in sudden coronary death.
Pharmacotherapy in inherited and acquired ventricular arrhythmia in structurally normal adult hearts.
Predicting the risk of sudden cardiac death.
Primary and secondary prevention of sudden cardiac death: the role of the implantable cardioverter defibrillator.
Profiling risk from arrhythmic or hemodynamic death.
Prospective risk stratification of sudden cardiac death in Marfan's syndrome.
QT prolongation and sudden cardiac death risk in hypertrophic cardiomyopathy.
Risk factors for atrioventricular tachycardia degenerating to atrial flutter/fibrillation in the young with Wolff-Parkinson-White.
Risk stratification and primary prevention of sudden cardiac death: sudden death prevention.
Risk Stratification for Sudden Cardiac Death.
Role of antiarrhythmic therapy in patients at risk for sudden cardiac death: an evidence-based review.
Role of risk stratification and genetics in sudden cardiac death.
Sudden cardiac death: a retrospective and prospective study.
Sudden cardiac death: from molecular biology and cellular electrophysiology to therapy.
Sudden cardiac death: implantable cardioverter defibrillators and pharmacological treatments.
Sudden death in patients with chronic bifascicular block.
Sudden Death Mechanisms in Non-ischemic Cardiomyopathies; Insights gleaned from clinical implantable cardioverter-defibrillator trials.
The Midlands Trial of Empirical Amiodarone versus Electrophysiology-guided Interventions and Implantable Cardioverter-defibrillators (MAVERIC): a multi-centre prospective randomised clinical trial on the secondary prevention of sudden cardiac death.
The problem of indeterminate microvolt T-wave alternans results in patients with left ventricular dysfunction referred for implantable cardioverter-defibrillator implantation in the primary prevention of sudden cardiac death.
Toward Miniaturization of Defibrillators: Design of a Defibrillation Charge/Discharge Circuit.
Trans-fatty acids and sudden cardiac death.
Ventricular Arrhythmias and Sudden Cardiac Death.
Ventricular tachycardia-inducibility predicts arrhythmic events in post-myocardial infarction patients with low ejection fraction. A systematic review and meta-analysis.
[Automatic external defibrillator--mode of operation and clinical use]
[Effect of physical activity on incidence of sudden cardiac death. Study of the Berlin-Reinickendorf and Berlin-Spandau population]
[Negative result of microvolt T-wave alternans test is helpful in scheduling the order of cardioverter-defibrillator implantation in primary prevention of sudden cardiac death in individuals with the left ventricular systolic dysfunction].
[Risk-stratification strategy for sudden cardiac death in the very young children with asymptomatic ventricular preexcitation].
[Sudden cardiac death: epidemiology and modern therapy]
[The electrophysiological study and implantable cardioverter defibrillator therapy for the patients with Brugada syndrome]
[Ventricular arrhythmias and sudden cardiac death in acute myocardial infarct in the era of thrombolytics]
[Ventricular arrhythmias and sudden cardiac death]
Ventricular Premature Complexes
Brief sympathetic activation precedes the development of ventricular tachycardia and ventricular fibrillation in hibernating myocardium.
Catheter Ablation of Ventricular Tachycardia in Structural Heart Disease: Indications, Strategies, and Outcomes-Part II.
Catheter ablation to prevent sudden cardiac death.
Mechanism and prediction of sudden cardiac death in arrhythmia patients using electrophysiological studies.
Mitral valve prolapse: an underestimated cause of sudden cardiac death-a current review of the literature.
Myocarditis in the Athlete: Arrhythmogenic Substrates, Clinical Manifestations, Management, and Eligibility Decisions.
Predictors of Sudden Cardiac Death in Doberman Pinschers with Dilated Cardiomyopathy.
SCD-HeFT: Use of R-R interval statistics for long-term risk stratification for arrhythmic sudden cardiac death.
Sudden death in patients with chronic bifascicular block.
The effect of aldosterone antagonists for ventricular arrhythmia: a meta-analysis.
The prevalence and clinical significance of premature ventricular beats in the athlete.
[Premature ventricular beats in young athletes: interpretation and diagnostic pathway].
Vertigo
Association between endothelial dysfunction and otoneurological symptoms in children with sickle cell disease.
Eye movements in patients with superior canal dehiscence syndrome align with the abnormal canal.
Superior canal dehiscence reveals concomitant unilateral utricular loss (UUL).
Underwater Endoscopic Repair of Superior Canal Dehiscence.
Virus Diseases
A Meta-Analysis on the Seroprevalence of Parvovirus B19 among Patients with Sickle Cell Disease.
Hepatitis B and C viral markers in patients with sickle cell disease in Ibadan, Nigeria.
Potential Implications of a Type 1 Interferon Gene Signature on COVID-19 Severity and Chronic Inflammation in Sickle Cell Disease.
Soluble CD-4 and CD-8 as markers of immunological activation in renal transplant recipients.
Superimposed Hepatitis C Virus in Sickle Cell Disease Pregnant Woman.
Vascular Permeability Drives Susceptibility to Influenza Infection in a Murine Model of Sickle Cell Disease.
Vision Disorders
Ocular manifestations of sickle cell disease.
Risk factors for visual impairment in patients with sickle cell disease in London.
Visual cortex changes in children with sickle cell disease and normal visual acuity: a multimodal magnetic resonance imaging study.
Vitamin A Deficiency
Vitamin A deficiency induces endoplasmic reticulum stress and apoptosis in pancreatic islet cells: Implications of stearoyl-CoA desaturase 1-mediated oleic acid synthesis.
Vitamin B 12 Deficiency
Methylenetetrahydrofolate Reductase (MTHFR) C677T Polymorphism and Subacute Combined Degeneration: Revealing a Genetic Predisposition.
Subacute combined degeneration of the spinal cord in a patient abusing nitrous oxide and self-medicating with cyanocobalamin.
Subacute combined degeneration of the spinal cord in cblC disorder despite treatment with B12.
Subacute combined degeneration: clinical, electrophysiological, and magnetic resonance imaging findings.
The Level of Serum Pepsinogen in Diagnosing and Evaluating the Severity of Subacute Combined Degeneration Due to Vitamin B12 Deficiency.
[A case of subacute combined degeneration of the spinal cord diagnosed by characteristic findings of magnetic resonance imaging: case report and review of 22 cases]
Vitamin B 6 Deficiency
Dependence of pyridoxine metabolism on riboflavin status in sickle cell patients.
Hyperhomocysteinemia is associated with low plasma pyridoxine levels in children with sickle cell disease.
Vitamin D Deficiency
Association of vitamin D deficiency with heart failure and sudden cardiac death in a large cross-sectional study of patients referred for coronary angiography.
Frequency and risk factors of endocrine complications in Turkish children and adolescents with sickle cell anemia.
Hemoglobin Alters Vitamin Carrier Uptake and Vitamin D Metabolism in Proximal Tubule Cells: Implications for Sickle Cell Disease.
Impact of Hydroxyurea on Anthropometry and Serum 25-Hydroxyvitamin D Among Children With Sickle Cell Disease.
Mechanisms of Bone Impairment in Sickle Bone Disease.
Multiple Sclerosis: Lipids, Lymphocytes, and Vitamin D.
Prevalence of vitamin d deficiency in sickle cell disease: a systematic review.
Response to Long-term Vitamin D Therapy for Bone Disease in Children With Sickle Cell Disease.
Sickle cell bone disease: response to vitamin D and calcium.
The association between vitamin D deficiency and hospitalization outcomes in pediatric patients with sickle cell disease.
Vitamin D and Nonskeletal Complications among Egyptian Sickle Cell Disease Patients.
Vitamin D deficiency and acute vaso-occlusive complications in children with sickle cell disease.
Vitamin D deficiency influences fatty acid metabolism.
Vitamin D deficiency is associated with sudden cardiac death, combined cardiovascular events, and mortality in haemodialysis patients.
Vitamin D supplementation and pain-related emergency department visits in children with sickle cell disease.
Vitamin D supplementation for sickle cell disease.
Vitamin E Deficiency
Subacute combined degeneration associated with vitamin E deficiency due to small bowel obstruction: A case report.
Vitiligo
Suppression of FADS1 induces ROS generation, cell cycle arrest, and apoptosis in melanocytes: implications for vitiligo.
Vitreous Hemorrhage
Ocular manifestations of sickle cell disease and genetic susceptibility for refractive errors.
Wolff-Parkinson-White Syndrome
Aborted sudden cardiac death as first presentation of Wolff-Parkinson-White syndrome.
Cardiac Screening for High Risk Sudden Cardiac Death in School-Aged Children.
Electrocardiogram Screening for Disorders That Cause Sudden Cardiac Death in Asymptomatic Children: A Meta-analysis.
Mechanism and prediction of sudden cardiac death in arrhythmia patients using electrophysiological studies.
Medico-legal perspectives on sudden cardiac death in young athletes.
Ventricular pre-excitation: symptomatic and asymptomatic children have the same potential risk of sudden cardiac death.
Wolff-Parkinson-White syndrome and sudden cardiac death.
Wound Infection
Review of Sickle Cell Disease and Spinal Pathology.
Zika Virus Infection
Inositol requiring enzyme 1? promotes Zika virus infection through regulating stearoyl-CoA desaturase 1 mediated lipid metabolism.