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The American Journal of Medicine|May 4, 2004
Effects of ACE gene insertion/deletion polymorphism on response to spironolactone in patients with chronic heart failureMariantonietta Cicoira, Andrea Rossi, Stefano Bonapace, et al.The Journal of Invasive Cardiology|June 2, 2007
Recurrent in-stent restenosis is not associated with the angiotensin-converting enzyme D/I, angiotensinogen Thr174Met and Met235Thr, and the angiotensin-II receptor 1 A1166C polymorphismC Michael Gross, Andreas Perrot, Christian Geier, et al.International Journal of Cardiology|December 22, 2009
Mutational analysis of the PITX2 and NKX2-5 genes in patients with idiopathic atrial fibrillationLeif-Hendrik Boldt, Maximilian G Posch, Andreas Perrot, et al.Pediatric Cardiology|October 31, 2006
Mutations in the EGF-CFC gene cryptic are an infrequent cause of congenital heart diseaseCemil Ozcelik, Nana Bit-Avragim, Anna Panek, et al.Human Mutation|May 18, 2006
Novel sequence variants in dysferlin-deficient muscular dystrophy leading to mRNA decay and possible C2-domain misfoldingKatrin Wenzel, Miriam Carl, Andreas Perrot, et al.International Journal of Cardiology|June 23, 2009
Plasma HER2 levels are not associated with cardiac function or hypertrophy in control subjects and heart failure patientsMaximilian G Posch, Anna Panek, Andrea Kersten, et al.Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|March 29, 2006
Hypertrophic cardiomyopathy in a Portuguese population: mutations in the myosin-binding protein C geneNuno Cardim, Andreas Perrot, Susana Santos, et al.Cardiovascular Research|August 12, 2003
Expression profiling of human idiopathic dilated cardiomyopathyRafal Grzeskowiak, Henning Witt, Mario Drungowski, et al.Heart Rhythm|March 28, 2009
Genetic deletion of arginine 14 in phospholamban causes dilated cardiomyopathy with attenuated electrocardiographic R amplitudesMaximilian G Posch, Andreas Perrot, Christian Geier, et al.European Journal of Human Genetics : EJHG|October 31, 2002
Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathyZhyldyz T Kabaeva, Andreas Perrot, Bastian Wolter, et al.Pageof 7