Back
Speaker illustration

Doctor Robert Sepp

University of Szeged, Szeged (Hungary)

Presentations

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

Access
Like
Thumbnail

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

Access
Like
Thumbnail

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

Access
Like
Thumbnail

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

Access
Like
Thumbnail

ESC 365 is supported by

logo Bristol Myers Squibb Explore sponsored resources
logo Novo Nordisk Explore sponsored resources