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Circulation|March 31, 2004
Left cardiac sympathetic denervation in the management of high-risk patients affected by the long-QT syndromePeter J Schwartz, Silvia G Priori, Marina Cerrone, et al.
Journal of the American College of Cardiology|July 10, 2003
Modulating effects of age and gender on the clinical course of long QT syndrome by genotypeWojciech Zareba, Arthur J Moss, Emanuela H Locati, et al.
JAMA Cardiology|March 30, 2022
Outcomes of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia Treated With β-BlockersAndrea Mazzanti, Deni Kukavica, Alessandro Trancuccio, et al.
JAMA|September 14, 2006
Risk of aborted cardiac arrest or sudden cardiac death during adolescence in the long-QT syndromeJenny B Hobbs, Derick R Peterson, Arthur J Moss, et al.
Journal of the American College of Cardiology|March 14, 2007
Long QT syndrome and pregnancyRahul Seth, Arthur J Moss, Scott McNitt, et al.
American Heart Journal|November 24, 2007
High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinicsJ Peter van Tintelen, Robert M W Hofstra, Hilga Katerberg, et al.
Circulation|April 23, 2008
Risk factors for aborted cardiac arrest and sudden cardiac death in children with the congenital long-QT syndromeIlan Goldenberg, Arthur J Moss, Derick R Peterson, et al.
Journal of the American Heart Association|May 28, 2015
Use of whole exome sequencing for the identification of Ito-based arrhythmia mechanism and therapyAmy C Sturm, Crystal F Kline, Patric Glynn, et al.
Cardiovascular Journal of Africa|September 6, 2014
Rationale and design of the Pan-African Sudden Cardiac Death survey: the Pan-African SCD studyAimé Bonny, Marcus Ngantcha, Sylvie Ndongo Amougou, et al.
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