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CJC Open|February 24, 2026
"I Am a Quarterback": A Mixed-Methods Study of Death Investigators' Communication with Family Members of Young Sudden Cardiac Death VictimsKatherine L Mason, Katherine S Allan, June Carroll, et al.
Heart Rhythm|September 7, 2010
Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac deathElena Burashnikov, Ryan Pfeiffer, Héctor Barajas-Martinez, et al.
Journal of Arrhythmia|February 25, 2026
Contemporary Perspectives on J-Wave Syndromes: An Expert Consensus StatementKoonlawee Nademanee, Arthur A Wilde, Michael J Ackerman, et al.
Ebiomedicine|April 8, 2020
Identification, clinical manifestation and structural mechanisms of mutations in AMPK associated cardiac glycogen storage diseaseDan Hu, Dong Hu, Liwen Liu, et al.
European Journal of Cardiovascular Prevention and Rehabilitation : Official Journal of the European Society of Cardiology, Working Groups on Epidemiology & Prevention and Cardiac Rehabilitation and Exercise Physiology|May 13, 2010
Sports and arrhythmias: a report of the International Workshop Venice Arrhythmias 2009Franco Giada, Alessandro Biffi, David S Cannom, et al.
Journal of the American College of Cardiology|July 7, 2014
Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndromeDan Hu, Hector Barajas-Martínez, Ryan Pfeiffer, et al.
The New England Journal of Medicine|April 1, 2014
Survival with cardiac-resynchronization therapy in mild heart failureIlan Goldenberg, Valentina Kutyifa, Helmut U Klein, et al.
European Heart Journal|September 24, 2021
Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic deathRoddy Walsh, Arnon Adler, Ahmad S Amin, et al.
Circulation|January 28, 2020
An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT SyndromeArnon Adler, Valeria Novelli, Ahmad S Amin, et al.
American Journal of Medical Genetics. Part A|December 17, 2019
Utilization of the 2017 diagnostic criteria for hEDS by the Toronto GoodHope Ehlers-Danlos syndrome clinic: A retrospective reviewLaura McGillis, Nimish Mittal, Daniel Santa Mina, et al.
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