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Heart Rhythm|November 4, 2024
Long-term prognosis of patients with an SCN5A loss-of-function variant and progressive cardiac conduction disorder or Brugada syndromeFenna Tuijnenburg, Virginnio M Proost, Aurélie Thollet, et al.Heart Rhythm|November 13, 2023
Type 3 long QT syndrome: Is the effectiveness of treatment with beta-blockers population-specific?Alexis Hermida, Jean-Baptiste Gourraud, Isabelle Denjoy, et al.Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|April 20, 2010
Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practiceVeronique Fressart, Guillaume Duthoit, Erwan Donal, et al.Circulation|August 18, 2012
Parental electrocardiographic screening identifies a high degree of inheritance for congenital and childhood nonimmune isolated atrioventricular blockAlban-Elouen Baruteau, Albin Behaghel, Swanny Fouchard, et al.JACC. Clinical Electrophysiology|July 22, 2023
Left Ventricular Abnormal Substrate in Brugada SyndromeGhassen Cheniti, Michel Haissaguerre, Christian Dina, et al.Cardiovascular Research|August 4, 2025
Phenotypic spectrum of cardiac conduction disturbance and cardiomyopathy linked to titin canonical splice-site variantsTaisuke Ishikawa, Hiroki Kimoto, Akiko Seki, et al.Circulation|November 23, 2006
Outcome after implantation of a cardioverter-defibrillator in patients with Brugada syndrome: a multicenter studyFrédéric Sacher, Vincent Probst, Yoshito Iesaka, et al.Journal of the American College of Cardiology|January 17, 2015
Role of electrophysiological studies in predicting risk of ventricular arrhythmia in early repolarization syndromeSaagar Mahida, Nicolas Derval, Frederic Sacher, et al.Human Molecular Genetics|February 5, 2015
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndromeSolena Le Scouarnec, Matilde Karakachoff, Jean-Baptiste Gourraud, et al.American Journal of Human Genetics|August 16, 2016
Biallelic PPA2 Mutations Cause Sudden Unexpected Cardiac Arrest in InfancyAnne Guimier, Christopher T Gordon, François Godard, et al.Pageof 21