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Plos One|August 23, 2011
Genotype at the P554L variant of the hexose-6 phosphate dehydrogenase gene is associated with carotid intima-medial thicknessThahira J Rahman, Elizabeth A Walker, Bongani M Mayosi, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|June 25, 2013
Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7Alexa M C Vermeer, Klaartje van Engelen, Alex V Postma, et al.
Catheterization and Cardiovascular Interventions : Official Journal of the Society for Cardiac Angiography & Interventions|February 14, 2015
Impact of age on access site-related outcomes in 469,983 percutaneous coronary intervention procedures: Insights from the British Cardiovascular Intervention SocietySimon G Anderson, Karim Ratib, Phyo K Myint, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Genetic variants associated with myocardial infarction risk factors in over 8000 individuals from five ethnic groups: The INTERHEART Genetics StudySonia S Anand, Changchun Xie, Guillaume Paré, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society|April 10, 2019
Does rhythm matter in acute heart failure? An insight from the British Society for Heart Failure National AuditSimon G Anderson, Ahmad Shoaib, Phyo Kyaw Myint, et al.
The Journal of Clinical Endocrinology and Metabolism|September 21, 2006
Association between aldosterone production and variation in the 11beta-hydroxylase (CYP11B1) geneHelen Imrie, Marie Freel, Bongani M Mayosi, et al.
Frontiers in Bioengineering and Biotechnology|June 26, 2020
A Patient-Specific CFD Pipeline Using Doppler Echocardiography for Application in Coarctation of the Aorta in a Limited Resource Clinical ContextLiam Swanson, Benjamin Owen, Amir Keshmiri, et al.
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