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Heart (British Cardiac Society)|May 13, 2011
The site of origin of torsade de pointesEdo Y Birati, Bernard Belhassen, Abdennasser Bardai, et al.Journal of Molecular and Cellular Cardiology|July 28, 2010
The pathophysiological mechanism underlying Brugada syndrome: depolarization versus repolarizationArthur A M Wilde, Pieter G Postema, José M Di Diego, et al.Korean Circulation Journal|June 2, 2017
Idiopathic Polymorphic Ventricular Tachycardia: a "Benign Disease" with a Touch of Bad Luck?Sami ViskinCardiology Clinics|June 28, 2015
Syncope in Hereditary Arrhythmogenic SyndromesArnon Adler, Sami ViskinPacing and Clinical Electrophysiology : PACE|July 20, 2010
Successful ablation of right atriofascicular pathway guided by pathway potential recording despite catheter-induced mechanical pathway traumaBernard Belhassen, Sami ViskinCardiac Electrophysiology Clinics|June 5, 2016
Clinical Features of Genetic Cardiac Diseases Related to Potassium ChannelopathiesArnon Adler, Sami ViskinThe Canadian Journal of Cardiology|September 22, 2014
Near fatal ventricular fibrillation in Brugada syndrome despite presence of an implanted implantable cardioverter defibrillatorBernard Belhassen, Sami ViskinJournal of the American College of Cardiology|January 15, 2016
A Tale of 2 Diseases: The History of Long-QT Syndrome and Brugada SyndromeOfer Havakuk, Sami ViskinPacing and Clinical Electrophysiology : PACE|March 25, 2008
Channelopathies in children and adultsArthur A M WildeHeart Rhythm|July 5, 2015
Diagnostic value of T-wave morphology changes during "QT stretching" in patients with long QT syndromeEhud Chorin, Ofer Havakuk, Arnon Adler, et al.Pageof 60