Showing results (151-160 of 238) with videos related to
Sort By:
Pageof 24
International Journal of Cardiology|May 15, 2015
Genotype-dependent differences in age of manifestation and arrhythmia complications in short QT syndromeDaniel Toshio Harrell, Takashi Ashihara, Taisuke Ishikawa, et al.Circulation|January 2, 2009
High efficacy of beta-blockers in long-QT syndrome type 1: contribution of noncompliance and QT-prolonging drugs to the occurrence of beta-blocker treatment "failures"G Michael Vincent, Peter J Schwartz, Isabelle Denjoy, et al.Circulation Research|March 12, 2005
A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 geneSilvia G Priori, Sandeep V Pandit, Ilaria Rivolta, et al.Circulation Research|June 17, 2017
Allele-Specific Silencing of Mutant mRNA Rescues Ultrastructural and Arrhythmic Phenotype in Mice Carriers of the R4496C Mutation in the Ryanodine Receptor Gene (RYR2)Rossana Bongianino, Marco Denegri, Andrea Mazzanti, et al.Journal of the American College of Cardiology|June 27, 2002
Differential effects of beta-blockade on dispersion of repolarization in the absence and presence of sympathetic stimulation between the LQT1 and LQT2 forms of congenital long QT syndromeWataru Shimizu, Yasuko Tanabe, Takeshi Aiba, et al.Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|November 12, 2020
Left Ventricular Myocardial Work in Patients with Severe Aortic StenosisFederico Fortuni, Steele C Butcher, Frank van der Kley, et al.Circulation|July 3, 2002
Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardiaSilvia G Priori, Carlo Napolitano, Mirella Memmi, et al.Bioscience Reports|April 7, 2021
Identification of loss-of-function RyR2 mutations associated with idiopathic ventricular fibrillation and sudden deathXiaowei Zhong, Wenting Guo, Jinhong Wei, et al.Journal of Molecular Medicine (Berlin, Germany)|November 20, 2004
Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death?Jop H van Berlo, Willem G de Voogt, Anneke J van der Kooi, et al.Cardiovascular Research|January 19, 2010
Na+-dependent SR Ca2+ overload induces arrhythmogenic events in mouse cardiomyocytes with a human CPVT mutationSimon Sedej, Frank R Heinzel, Stefanie Walther, et al.Pageof 24