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Heart Rhythm|February 5, 2010
Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasiaBarbara Bauce, Andrea Nava, Giorgia Beffagna, et al.Journal of the American College of Cardiology|July 11, 2009
Risk factors and mode of death in isolated hypertrophic cardiomyopathy in childrenJamie A Decker, Joseph W Rossano, E O'Brian Smith, et al.Circulation. Cardiovascular Genetics|February 23, 2010
LAMP2 microdeletions in patients with Danon diseaseZhao Yang, Birgit H Funke, Linda H Cripe, et al.JAMA|October 19, 2006
Incidence, causes, and outcomes of dilated cardiomyopathy in childrenJeffrey A Towbin, April M Lowe, Steven D Colan, et al.Circulation|June 19, 1998
Age- and sex-related differences in clinical manifestations in patients with congenital long-QT syndrome: findings from the International LQTS RegistryE H Locati, W Zareba, A J Moss, et al.BMC Medical Genetics|October 30, 2007
Missense mutations in desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitroGiorgia Beffagna, Marzia De Bortoli, Andrea Nava, et al.Pediatric Cardiology|November 24, 2016
Utility of Echocardiography in the Assessment of Left Ventricular Diastolic Function and Restrictive Physiology in Children and Young Adults with Restrictive Cardiomyopathy: A Comparative Echocardiography-Catheterization StudyThomas D Ryan, Peace C Madueme, John L Jefferies, et al.Pediatrics|October 7, 2004
Clinical spectrum, morbidity, and mortality in 113 pediatric patients with mitochondrial diseaseFernando Scaglia, Jeffrey A Towbin, William J Craigen, et al.Circulation. Cardiovascular Genetics|August 12, 2011
Risk of syncope in family members who are genotype-negative for a family-associated long-QT syndrome mutationAlon Barsheshet, Arthur J Moss, Scott McNitt, et al.Circulation|February 2, 1999
Genetic and molecular basis of cardiac arrhythmias: impact on clinical management parts I and IIS G Priori, J Barhanin, R N Hauer, et al.Pageof 44