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International Journal of Cardiology|March 19, 2014
Bariatric surgery and its impact on cardiovascular disease and mortality: a systematic review and meta-analysisChun Shing Kwok, Ashish Pradhan, Muhammad A Khan, et al.Nature Communications|July 27, 2013
Detection of microwave phase variation in nanometre-scale magnetic heterostructuresW E Bailey, C Cheng, R Knut, et al.European Journal of Human Genetics : EJHG|April 25, 2020
Association of congenital cardiovascular malformation and neuropsychiatric phenotypes with 15q11.2 (BP1-BP2) deletion in the UK BiobankSimon G Williams, Apostol Nakev, Hui Guo, et al.Scientific Reports|September 3, 2020
Heritability of haemodynamics in the ascending aortaKathryn A McGurk, Benjamin Owen, William D Watson, 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.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.Annals of Human Genetics|August 14, 2013
Quantitative variation in plasma angiotensin-I converting enzyme activity shows allelic heterogeneity in the ABO blood group locusChikashi Terao, Nervana Bayoumi, Colin A McKenzie, et al.The Journal of Invasive Cardiology|August 6, 2013
Provision of gastroprotective medication and bleeding risk following acute coronary syndromeAthar Badar, Jennifer Scaife, Andrew T Yan, et al.Heart (British Cardiac Society)|April 2, 2010
22q11.2 Deletion Syndrome is under-recognised in adult patients with tetralogy of Fallot and pulmonary atresiaKlaartje van Engelen, Ana Topf, Bernard D Keavney, et al.Human Mutation|January 26, 2012
Nonsynonymous variants in the SMAD6 gene predispose to congenital cardiovascular malformationHuay L Tan, Elise Glen, Ana Töpf, et al.Pageof 8