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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 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.
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.
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