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Journal of the American College of Cardiology|December 27, 2014
Disturbance in Z-disk mechanosensitive proteins induced by a persistent mutant myopalladin causes familial restrictive cardiomyopathyAnne-Cecile Huby, Uzmee Mendsaikhan, Ken Takagi, et al.
Heart Rhythm|September 21, 2010
Trigger-specific risk factors and response to therapy in long QT syndrome type 2James A Kim, Coeli M Lopes, Arthur J Moss, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|July 27, 2016
The Twin Study of Negative Valence Emotional ConstructsDever M Carney, Elizabeth Moroney, Laura Machlin, et al.
Heart (British Cardiac Society)|July 16, 2004
Echocardiographic predictors of adverse clinical events in children with dilated cardiomyopathy: a prospective clinical studyC J McMahon, S F Nagueh, R S Eapen, et al.
Human Molecular Genetics|October 21, 2005
A cardiac myosin binding protein C mutation in the Maine Coon cat with familial hypertrophic cardiomyopathyKathryn M Meurs, Ximena Sanchez, Ryan M David, et al.
Circulation. Cardiovascular Imaging|December 19, 2023
Utility of Left and Right Ventricular Strain in Arrhythmogenic Right Ventricular Cardiomyopathy: A Prospective Multicenter RegistryMayooran Namasivayam, Philippe B Bertrand, Samuel Bernard, et al.
American Journal of Physiology. Heart and Circulatory Physiology|November 29, 2013
Cardiac-specific VLCAD deficiency induces dilated cardiomyopathy and cold intoleranceDingding Xiong, Huamei He, Jeanne James, et al.
Artificial Organs|September 24, 2004
Outcomes of congenital heart surgery patients after extracorporeal life support at Texas Children's HospitalAkif Undar, E Dean McKenzie, Mary C McGarry, et al.
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