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Journal of Medical Genetics|February 9, 2000
First description of germline mosaicism in familial hypertrophic cardiomyopathyJ F Forissier, P Richard, S Briault, et al.Journal of the American College of Cardiology|January 15, 2000
Lack of association between polymorphisms of eight candidate genes and idiopathic dilated cardiomyopathy: the CARDIGENE studyL Tiret, C Mallet, O Poirier, et al.Circulation|October 23, 1997
Prognostic value of bisoprolol-induced hemodynamic effects in heart failure during the Cardiac Insufficiency BIsoprolol Study (CIBIS)P Lechat, S Escolano, J L Golmard, et al.Heart (British Cardiac Society)|July 16, 2004
Danon's disease as a cause of hypertrophic cardiomyopathy: a systematic surveyP Charron, E Villard, P Sébillon, et al.Clinical Research in Cardiology : Official Journal of the German Cardiac Society|October 27, 2018
Mode of presentation and mortality amongst patients hospitalized with heart failure? A report from the First Euro Heart Failure SurveyAhmad Shoaib, M Farag, J Nolan, et al.Journal of Molecular and Cellular Cardiology|July 20, 2000
Homozygotes for a R869G mutation in the beta -myosin heavy chain gene have a severe form of familial hypertrophic cardiomyopathyP Richard, P Charron, C Leclercq, et al.Heart (British Cardiac Society)|March 8, 2011
Plakophilin 2A is the dominant isoform in human heart tissue: consequences for the genetic screening of arrhythmogenic right ventricular cardiomyopathyE Gandjbakhch, P Charron, V Fressart, et al.Circulation|December 29, 2005
Deficiency of the 5-hydroxytryptamine transporter gene leads to cardiac fibrosis and valvulopathy in miceA Mekontso-Dessap, F Brouri, O Pascal, et al.Deutsche Medizinische Wochenschrift (1946)|September 29, 2005
[Adherence to guidelines in CHF therapy in Germany]M Flesch, M Komajda, P Lapuerta, et al.Archives of Cardiovascular Diseases|July 29, 2008
Treatment of heart failure with preserved systolic functionP de Groote, D Herpin, F Diévart, et al.Pageof 36