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Cardiovascular Research|March 17, 2004
A trafficking defective, Brugada syndrome-causing SCN5A mutation rescued by drugsCarmen R Valdivia, David J Tester, Benjamin A Rok, et al.
Journal of Cardiovascular Electrophysiology|March 18, 2026
Cardiac Myosin Inhibitors and Incident Atrial Fibrillation in Hypertrophic Cardiomyopathy: Systematic Review and Meta-AnalysisPaschalis Karakasis, Cyrus Nouraee, Eduardo Martinez-Gomez, et al.
Journal of Molecular and Cellular Cardiology|February 15, 2008
A splice site mutation in hERG leads to cryptic splicing in human long QT syndromeQiuming Gong, Li Zhang, Arthur J Moss, et al.
Circulation. Genomic and Precision Medicine|February 18, 2018
Yield of the RYR2 Genetic Test in Suspected Catecholaminergic Polymorphic Ventricular Tachycardia and Implications for Test InterpretationJamie D Kapplinger, Krishna N Pundi, Nicholas B Larson, et al.
Circulation|December 20, 2011
Connexin43 mutation causes heterogeneous gap junction loss and sudden infant deathDavid W Van Norstrand, Angeliki Asimaki, Clio Rubinos, et al.
European Heart Journal|September 11, 2014
Electromechanical window negativity in genotyped long-QT syndrome patients: relation to arrhythmia riskRachel M A ter Bekke, Kristina H Haugaa, Arthur van den Wijngaard, et al.
British Journal of Sports Medicine|January 6, 2016
Electrocardiographic abnormalities in elite high school athletes: comparison to adolescent hypertrophic cardiomyopathyAlex J Thompson, Bryan C Cannon, Philip L Wackel, et al.
Journal of the American College of Cardiology|December 11, 2020
Echocardiography-Guided Risk Stratification for Long QT SyndromeAlan Sugrue, Martin van Zyl, Nick Enger, et al.
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