Doctor Robert Sepp
University of Szeged, Szeged (Hungary)
Identification of a novel actin gene mutation, ACTC1 p.Asn94Ile, in a family with cardiomyopathy and conduction disease
Event: Heart Failure 2024
Topic: Hypertrophic Cardiomyopathy
Session: Myocardial disease - clinical 7
Direct abnormal communications between septal perforator arteries and cardiac chambers: a potential source of serious complications during alcohol septal ablation in hypertrophic cardiomyopathy
Event: Heart Failure 2024
Topic: Hypertrophic Cardiomyopathy
Session: ePosters in myocardial disease 4
Extreme myocardial fibrosis caused by a novel cardiac actin gene (ACTC1) p.Asn94Ile mutation leading to hypertrophic cardiomyopathy and progressive conduction disease
Event: Heart Failure 2024
Topic: Clinical
Session: Cardiomyopathies - hypertrophic cardiomyopathy and amyloidosis
Glycogen storage disease of unknown origin causing hypertrophic cardiomyopathy phenocopy and conduction disorder
Event: Heart Failure 2024
Topic: Clinical
Session: Cardiomyopathies - hypertrophic cardiomyopathy and amyloidosis
