Showing results (21-30 of 64) with videos related to

Sort By:
Pageof 7
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.
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.
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