Showing results (121-130 of 240) with videos related to

Sort By:
Pageof 24
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|October 12, 2023
Transforming Drug Development for Neurological Disorders: Proceedings from a Multidisease Area WorkshopDiane Stephenson, Ramona Belfiore-Oshan, Yashmin Karten, et al.
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.
Scientific Reports|September 3, 2020
Heritability of haemodynamics in the ascending aortaKathryn A McGurk, Benjamin Owen, William D Watson, et al.
Open Heart|October 22, 2014
Major bleeding after percutaneous coronary intervention and risk of subsequent mortality: a systematic review and meta-analysisChun Shing Kwok, Sunil V Rao, Phyo K Myint, 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.
Scientific Reports|September 21, 2019
Marked variation in heritability estimates of left ventricular mass depending on modality of measurementRichard M Nethononda, Kathryn A McGurk, Polly Whitworth, 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.
Journal of Molecular and Cellular Cardiology|June 16, 2015
Genetic variants associated with risk of atrial fibrillation regulate expression of PITX2, CAV1, MYOZ1, C9orf3 and FANCCRuairidh I R Martin, Mahsa Sheikhali Babaei, Mun-Kit Choy, et al.
Pageof 24