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The Journal of Clinical Investigation|February 5, 2008
Cholesterol in islet dysfunction and type 2 diabetesLiam R Brunham, Janine K Kruit, C Bruce Verchere, et al.
The Journal of Clinical Endocrinology and Metabolism|September 7, 2024
Predictors of Cardiovascular Disease in Individuals With Dysbetalipoproteinemia: A Prospective Study in the UK BiobankMartine Paquette, Mark Trinder, Simon-Pierre Guay, et al.
Pharmacogenetics and Genomics|August 1, 2015
Pharmacogenetic versus clinical dosing of warfarin in individuals of Chinese and African-American ancestry: assessment using data simulationNicholas L X Syn, Soo-Chin Lee, Liam R Brunham, et al.
Atherosclerosis|December 15, 2021
Polygenic architecture and cardiovascular risk of familial combined hyperlipidemiaMark Trinder, Diana Vikulova, Simon Pimstone, et al.
The Canadian Journal of Cardiology|December 29, 2020
The Interplay Between Titin, Polygenic Risk, and Modifiable Cardiovascular Risk Factors in Atrial FibrillationKate Huang, Mark Trinder, Thomas M Roston, et al.
European Heart Journal|August 28, 2023
Recommendations for statin management in primary prevention: disparities among international risk scoresG B John Mancini, Arnold Ryomoto, Eunice Yeoh, et al.
Cardiovascular Research|June 8, 2018
Role of genetics in the prediction of statin-associated muscle symptoms and optimization of statin use and adherenceLiam R Brunham, Steven Baker, Andrew Mammen, et al.
The Canadian Journal of Cardiology|August 29, 2021
Familial Hypercholesterolemia, Familial Combined Hyperlipidemia, and Elevated Lipoprotein(a) in Patients With Premature Coronary Artery DiseaseDiana N Vikulova, Mark Trinder, G B John Mancini, et al.
Journal of Clinical Lipidology|November 19, 2017
Increased prevalence of clinical and subclinical atherosclerosis in patients with damaging mutations in ABCA1 or APOA1Omar Abdel-Razek, Singh N Sadananda, Xuan Li, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 24, 2003
Efflux and atherosclerosis: the clinical and biochemical impact of variations in the ABCA1 geneRoshni R Singaraja, Liam R Brunham, Henk Visscher, et al.
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