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Annals of Human Genetics|November 4, 2005
Possible association of the human KCNE1 (minK) gene and QT interval in healthy subjects: evidence from association and linkage analyses in Israeli familiesY Friedlander, M Vatta, N Sotoodehnia, et al.Journal of Cardiac Failure|March 8, 2006
Outpatient continuous parenteral inotropic therapy as bridge to transplantation in children with advanced heart failureJack F Price, Jeffrey A Towbin, William J Dreyer, et al.Genes|January 23, 2024
Exploring the Regulation and Function of Rpl3l in the Development of Early-Onset Dilated Cardiomyopathy and Congestive Heart Failure Using Systems Genetics ApproachAkhilesh K Bajpai, Qingqing Gu, Buyan-Ochir Orgil, et al.The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|January 22, 2004
Late pacemaker requirement after pediatric orthotopic heart transplantation may predict the presence of transplant coronary artery diseaseBryan C Cannon, Susan W Denfield, Richard A Friedman, et al.Circulation|June 22, 1999
Familial hypertrophic cardiomyopathy in maine coon cats: an animal model of human diseaseM D Kittleson, K M Meurs, M J Munro, et al.Blood|May 17, 2017
Association between diffuse myocardial fibrosis and diastolic dysfunction in sickle cell anemiaOmar Niss, Robert Fleck, Fowe Makue, et al.Molecular Genetics and Metabolism|August 24, 2010
Milder clinical course of Type IV 3-methylglutaconic aciduria due to a novel mutation in TMEM70Oleg A Shchelochkov, Fang-Yuan Li, Jing Wang, et al.Circulation|March 3, 2004
Arrhythmogenic right ventricular cardiomyopathy causing sudden cardiac death in boxer dogs: a new animal model of human diseaseCristina Basso, Philip R Fox, Kathryn M Meurs, et al.Circulation|June 1, 1993
X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locusJ A Towbin, J F Hejtmancik, P Brink, et al.JAMA|November 17, 2001
Postmortem molecular analysis of SCN5A defects in sudden infant death syndromeM J Ackerman, B L Siu, W Q Sturner, et al.Pageof 44