Peptides are fragments of proteins that carry out biological functions. They act as signaling
entities via all domains of life and interfere with protein-protein interactions, which are …

Arrhythmogenic cardiomyopathy (ACM) is a primary disease of the myocardium,
predominantly caused by genetic defects in proteins of the cardiac intercalated disc …

Background: There is a paucity of data regarding the phenotype of dilated cardiomyopathy
(DCM) gene variants in the general population. We aimed to determine the frequency and …

Background Inherited cardiomyopathies present with broad variation of phenotype. Data are
limited regarding genetic screening strategies and outcomes associated with predicted …

Inherited cardiomyopathies are frequent causes of sudden cardiac death (SCD), especially
in young patients. Despite at the autopsy they usually have distinctive microscopic and/or …

Non-ischemic cardiomyopathy (NICM) is one of the most important entities for arrhythmias
and sudden cardiac death (SCD). Previous studies suggest a lower benefit of implantable …

Arrhythmogenic cardiomyopathy (ACM) is an inherited cardiomyopathy histologically
characterized by the replacement of myocardium by fibrofatty infiltration, cardiomyocyte loss …

Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiomyopathy
characterized by fibrofatty infiltration of predominantly the right ventricular (RV) myocardium …

Arrhythmogenic cardiomyopathy (ACM) is a cardiomyopathy characterized by the
occurrence of a high risk of life-threatening ventricular arrhythmias and sudden cardiac …

Inherited cardiovascular diseases are highly heterogeneous conditions with multiple genetic
loci involved. The application of advanced molecular tools, such as Next Generation …