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Journal of the American Society of Nephrology : JASN|July 3, 2010
HLA has strongest association with IgA nephropathy in genome-wide analysisJohn Feehally, Martin Farrall, Anne Boland, et al.European Heart Journal. Cardiovascular Imaging|November 28, 2022
Left ventricular anatomy in obstructive hypertrophic cardiomyopathy: beyond basal septal hypertrophyUxio Hermida, David Stojanovski, Betty Raman, et al.Human Molecular Genetics|February 10, 2024
The genetic dissection of fetal haemoglobin persistence in sickle cell disease in NigeriaOyesola O Ojewunmi, Titilope A Adeyemo, Ajoke I Oyetunji, et al.Journal of the American Society of Nephrology : JASN|March 23, 2007
Association between angiotensin-converting enzyme gene polymorphisms and diabetic nephropathy: case-control, haplotype, and family-based study in three European populationsSamy Hadjadj, Lise Tarnow, Carol Forsblom, et al.Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|October 12, 2021
Incremental value of left atrial booster and reservoir strain in predicting atrial fibrillation in patients with hypertrophic cardiomyopathy: a cardiovascular magnetic resonance studyBetty Raman, Robert W Smillie, Masliza Mahmod, et al.Cardiovascular Research|April 16, 2008
The molecular phenotype of human cardiac myosin associated with hypertrophic obstructive cardiomyopathyAdam M Jacques, Natalia Briceno, Andrew E Messer, et al.Diabetes|October 27, 2006
Analysis of 14 candidate genes for diabetic nephropathy on chromosome 3q in European populations: strongest evidence for association with a variant in the promoter region of the adiponectin geneNathalie Vionnet, David Tregouët, Gbenga Kazeem, et al.Circulation Research|January 18, 2013
Living without creatine: unchanged exercise capacity and response to chronic myocardial infarction in creatine-deficient miceCraig A Lygate, Dunja Aksentijevic, Dana Dawson, et al.Journal of Medical Genetics|June 15, 2007
Genetic association analysis of inositol polyphosphate phosphatase-like 1 (INPPL1, SHIP2) variants with essential hypertensionAna Carolina Braga Marçano, Beverley Burke, Johannie Gungadoo, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|September 18, 2010
Coronary artery disease-related genetic variant on chromosome 10q11 is associated with carotid intima-media thickness and atherosclerosisStefan Kiechl, Ross C Laxton, Qingzhong Xiao, et al.Pageof 43