Showing results (561-570 of 723) with videos related to

Sort By:
Pageof 73
Circulation|August 16, 2013
Stroke or transient ischemic attack in patients with transvenous pacemaker or defibrillator and echocardiographically detected patent foramen ovaleChristopher V DeSimone, Paul A Friedman, Amit Noheria, et al.
Circulation. Arrhythmia and Electrophysiology|August 30, 2012
Loss of function of hNav1.5 by a ZASP1 mutation associated with intraventricular conduction disturbances in left ventricular noncompactionYutao Xi, Tomohiko Ai, Enno De Lange, et al.
Heart Rhythm|April 27, 2005
Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testingMichael J Ackerman, Igor Splawski, Jonathan C Makielski, et al.
Circulation. Arrhythmia and Electrophysiology|April 15, 2018
Left Ventricular Isovolumetric Relaxation Time Is Prolonged in Fetal Long-QT SyndromeSally-Ann B Clur, Arja S Vink, Susan P Etheridge, et al.
Biochemistry|October 25, 2012
High-risk long QT syndrome mutations in the Kv7.1 (KCNQ1) pore disrupt the molecular basis for rapid K(+) permeationDon E Burgess, Daniel C Bartos, Allison R Reloj, 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|November 12, 2022
Repeatability of ventricular arrhythmia characteristics on the exercise-stress test in RYR2-mediated catecholaminergic polymorphic ventricular tachycardiaPuck J Peltenburg, Sanjeev N J Pultoo, Kathryn E Tobert, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 25, 2018
Noncardiac genetic predisposition in sudden infant death syndromeBelinda Gray, David J Tester, Leonie Ch Wong, et al.
Circulation. Arrhythmia and Electrophysiology|September 21, 2010
A ZASP missense mutation, S196L, leads to cytoskeletal and electrical abnormalities in a mouse model of cardiomyopathyZhaohui Li, Tomohiko Ai, Kaveh Samani, et al.
Circulation. Arrhythmia and Electrophysiology|October 16, 2012
A novel disease gene for Brugada syndrome: sarcolemmal membrane-associated protein gene mutations impair intracellular trafficking of hNav1.5Taisuke Ishikawa, Akinori Sato, Cherisse A Marcou, et al.
Circulation Research|June 26, 2014
Characterization of SEMA3A-encoded semaphorin as a naturally occurring Kv4.3 protein inhibitor and its contribution to Brugada syndromeNicole J Boczek, Dan Ye, Eric K Johnson, et al.
Pageof 73