Showing results (31-40 of 240) with videos related to

Sort By:
Pageof 24
Lancet (London, England)|March 6, 2004
Four paraoxonase gene polymorphisms in 11212 cases of coronary heart disease and 12786 controls: meta-analysis of 43 studiesJeremy G Wheeler, Bernard D Keavney, Hugh Watkins, et al.
Journal of Human Hypertension|January 4, 2008
Common genetic variation in the type A endothelin-1 receptor is associated with ambulatory blood pressure: a family studyT Rahman, M Baker, D H Hall, et al.
Global Cardiology Science & Practice|February 11, 2025
Clinical assessment of patient outcomes post percutaneous pulmonary valve implantation: Insights from a single tertiary centreSushant Saluja, Daniel Myers, Bernard D Keavney, et al.
Scientific Reports|January 21, 2025
An in silico analysis of heart rate impact on wall shear stress hemodynamic parameters in aortic coarctationJie Wang, Emily Manchester, Alex Skillen, et al.
European Heart Journal|February 16, 2008
Genome-wide linkage analysis of electrocardiographic and echocardiographic left ventricular hypertrophy in families with hypertensionBongani M Mayosi, Peter J Avery, Martin Farrall, et al.
Plos Genetics|April 14, 2010
Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL ExpressionMichael S Cunnington, Mauro Santibanez Koref, Bongani M Mayosi, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|October 21, 2017
Cardiovascular, obstetric and neonatal outcomes in women with previous fontan repairS J Bonner, O Asghar, A Roberts, et al.
Physical Review Letters|December 31, 2005
Role of defect sites and Ga polarization in the magnetism of Mn-doped GaND J Keavney, S H Cheung, S T King, et al.
Prostaglandins & Other Lipid Mediators|April 26, 2022
Genetic analyses of circulating PUFA-derived mediators identifies heritable dihydroxyeicosatrienoic acid speciesKathryn A McGurk, Laura Farrell, Alexandra C Kendall, et al.
Kidney International|December 1, 1995
U.K. Prospective Diabetes Study. XV: Relationship of renin-angiotensin system gene polymorphisms with microalbuminuria in NIDDMC R Dudley, B Keavney, I M Stratton, et al.
Pageof 24