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Clinical Science (London, England : 1979)|September 27, 2005
A novel mutation in the cardiac myosin-binding protein C gene is responsible for hypertrophic cardiomyopathy with severe ventricular hypertrophy and sudden deathTetsuo Konno, Masami Shimizu, Hidekazu Ino, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|October 27, 2010
Impact of renin-angiotensin system polymorphisms on development of systolic dysfunction in hypertrophic cardiomyopathy. Evidence from a study of genotyped patientsAkira Funada, Tetsuo Konno, Noboru Fujino, et al.
Journal of Cardiology|December 3, 2014
Increased extent of myocardial fibrosis in genotyped hypertrophic cardiomyopathy with ventricular tachyarrhythmiasTakashi Fujita, Tetsuo Konno, Junichiro Yokawa, et al.
International Journal of Vascular Medicine|July 26, 2012
Expression and Function of Ephrin-B1 and Its Cognate Receptor EphB2 in Human Abdominal Aortic AneurysmAiji Sakamoto, Masaaki Kawashiri, Hatsue Ishibashi-Ueda, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|February 6, 2018
Late Gadolinium Enhancement for Prediction of Mutation-Positive Hypertrophic Cardiomyopathy on the Basis of Panel-Wide SequencingRyota Teramoto, Noboru Fujino, Tetsuo Konno, et al.
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