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European Heart Journal|February 22, 2014
Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathyKarin Y van Spaendonck-Zwarts, Anna Posafalvi, Maarten P van den Berg, et al.
Heart (British Cardiac Society)|January 1, 2016
Pregnancy course and outcomes in women with arrhythmogenic right ventricular cardiomyopathyAnke R Hodes, Crystal Tichnell, Anneline S J M Te Riele, et al.
Circulation. Arrhythmia and Electrophysiology|March 11, 2010
Arrhythmogenic right ventricular dysplasia/cardiomyopathy diagnostic task force criteria: impact of new task force criteriaMoniek G P J Cox, Jasper J van der Smagt, Maartje Noorman, et al.
European Journal of Heart Failure|January 26, 2013
Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experienceKarin Y van Spaendonck-Zwarts, Ingrid A W van Rijsingen, Maarten P van den Berg, et al.
Journal of the American College of Cardiology|June 4, 2011
Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noiseJamie D Kapplinger, Andrew P Landstrom, Benjamin A Salisbury, 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.
Brain : a Journal of Neurology|February 1, 2013
Recessive MYL2 mutations cause infantile type I muscle fibre disease and cardiomyopathyMarian A J Weterman, Peter G Barth, Karin Y van Spaendonck-Zwarts, et al.
Heart Rhythm|February 21, 2017
Cardiac phenotype and long-term prognosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia patients with late presentationAditya Bhonsale, Anneline S J M Te Riele, Abhishek C Sawant, et al.
European Journal of Heart Failure|June 19, 2019
Definition and treatment of arrhythmogenic cardiomyopathy: an updated expert panel reportPerry M Elliott, Aris Anastasakis, Angeliki Asimaki, et al.
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