Showing results (101-110 of 156) with videos related to

Sort By:
Pageof 16
Plos One|October 17, 2017
Association and clinical utility of NAT2 in the prediction of isoniazid-induced liver injury in Singaporean patientsSze Ling Chan, Angeline Poh Gek Chua, Folefac Aminkeng, et al.
The Canadian Journal of Cardiology|December 18, 2025
Canadian Cardiovascular Society Clinical Practice Update on Cardiogenetic TestingMelanie Care, Laura Arbour, Liam R Brunham, et al.
Thyroid : Official Journal of the American Thyroid Association|June 29, 2010
The Canadian Pharmacogenomics Network for Drug Safety: a model for safety pharmacologyColin J D Ross, Henk Visscher, Johanna Sistonen, et al.
Circulation Research|July 29, 2006
Specific mutations in ABCA1 have discrete effects on ABCA1 function and lipid phenotypes both in vivo and in vitroRoshni R Singaraja, Henk Visscher, Erick R James, et al.
Journal of the American College of Cardiology|July 27, 2019
Risk of Premature Atherosclerotic Disease in Patients With Monogenic Versus Polygenic Familial HypercholesterolemiaMark Trinder, Xuan Li, Maria Liza DeCastro, et al.
The Canadian Journal of Cardiology|July 11, 2024
Premature Acute Myocardial Infarction Treated With Invasive Revascularization: Comparing STEMI With NSTEMI in a Population-Based Study of Young PatientsThomas M Roston, Vivian Aghanya, Anamaria Savu, et al.
Clinical Genetics|April 13, 2011
Novel mutations in scavenger receptor BI associated with high HDL cholesterol in humansL R Brunham, I Tietjen, A E Bochem, et al.
Scientific Reports|November 15, 2018
CETP genetic variant rs1800777 (allele A) is associated with abnormally low HDL-C levels and increased risk of AKI during sepsisKelly Roveran Genga, Mark Trinder, HyeJin Julia Kong, et al.
Pageof 16