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Circulation|July 18, 2012
Early predictors of survival to and after heart transplantation in children with dilated cardiomyopathyBiagio A Pietra, Paul F Kantor, Heather L Bartlett, et al.Heart Rhythm|January 1, 2010
KCNE2 modulation of Kv4.3 current and its potential role in fatal rhythm disordersJie Wu, Wataru Shimizu, Wei-Guang Ding, et al.Journal of the American College of Cardiology|October 19, 2010
Nebulette mutations are associated with dilated cardiomyopathy and endocardial fibroelastosisEnkhsaikhan Purevjav, Jaquelin Varela, Micaela Morgado, et al.Journal of Cardiovascular Electrophysiology|December 18, 2003
Location of mutation in the KCNQ1 and phenotypic presentation of long QT syndromeWojciech Zareba, Arthur J Moss, Gloria Sheu, et al.Journal of the American College of Cardiology|February 4, 2012
Incidence of and risk factors for sudden cardiac death in children with dilated cardiomyopathy: a report from the Pediatric Cardiomyopathy RegistryElfriede Pahl, Lynn A Sleeper, Charles E Canter, et al.The American Journal of Cardiology|March 23, 2000
Clinical and genetic variables associated with acute arousal and nonarousal-related cardiac events among subjects with long QT syndromeR H Ali, W Zareba, A J Moss, et al.Molecular Genetics and Metabolism|October 22, 2003
Mutations in the muscle LIM protein and alpha-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosisBhagyalaxmi Mohapatra, Shinawe Jimenez, Jiuann Huey Lin, et al.Journal of Human Genetics|September 28, 2007
Danon disease presenting with dilated cardiomyopathy and a complex phenotypeMatthew R G Taylor, Lisa Ku, Dobromir Slavov, et al.Circulation|May 7, 1998
New mutations in the KVLQT1 potassium channel that cause long-QT syndromeH Li, Q Chen, A J Moss, et al.Circulation. Heart Failure|December 5, 2025
Cardiomyopathy-Associated Pathogenic Variants in Pediatric Myocarditis: A Study From the Pediatric Cardiomyopathy RegistryAlicia M Kamsheh, Stephanie M Ware, Surbhi Bhatnagar, et al.Pageof 44