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Plos One|July 11, 2013
Autosomal recessive transmission of MYBPC3 mutation results in malignant phenotype of hypertrophic cardiomyopathyYilu Wang, Zhimin Wang, Qi Yang, et al.Cardiovascular Research|February 5, 2019
Cardiac sodium-dependent glucose cotransporter 1 is a novel mediator of ischaemia/reperfusion injuryZhao Li, Vineet Agrawal, Mohun Ramratnam, et al.Circulation|December 26, 2007
Reversibility of PRKAG2 glycogen-storage cardiomyopathy and electrophysiological manifestationsCordula M Wolf, Michael Arad, Ferhaan Ahmad, et al.Journal of the American Heart Association|September 17, 2020
Diversity, Equity, and Inclusiveness in Medicine and Cardiology: Next Steps for <i>JAHA</i>Barry London, Ferhaan Ahmad, Daniel T Eitzman, et al.Epigenetics|November 27, 2024
Heavy alcohol consumption but not smoking predicts mortality in patients with acute coronary syndromeAllan Andersen, Steven R H Beach, Willem Philibert, et al.Circulation. Genomic and Precision Medicine|May 24, 2019
Establishment of Specialized Clinical Cardiovascular Genetics Programs: Recognizing the Need and Meeting Standards: A Scientific Statement From the American Heart AssociationFerhaan Ahmad, Elizabeth M McNally, Michael J Ackerman, et al.Plos One|December 10, 2016
Gene-Targeted Mice with the Human Troponin T R141W Mutation Develop Dilated Cardiomyopathy with Calcium DesensitizationMohun Ramratnam, Guy Salama, Ravi K Sharma, et al.Respirology (Carlton, Vic.)|April 4, 2018
S100A12 as a marker of worse cardiac output and mortality in pulmonary hypertensionArgyrios Tzouvelekis, Jose D Herazo-Maya, Changwan Ryu, et al.European Journal of Heart Failure|August 19, 2014
Malignant effects of multiple rare variants in sarcomere genes on the prognosis of patients with hypertrophic cardiomyopathyJizheng Wang, Yilu Wang, Yubao Zou, et al.Circulation|November 9, 2005
Increased alpha2 subunit-associated AMPK activity and PRKAG2 cardiomyopathyFerhaan Ahmad, Michael Arad, Nicolas Musi, et al.Pageof 5