Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is an inherited
cardiomyopathy that can lead to sudden cardiac death and heart failure. Our understanding …

Aims We sought to determine the influence of genotype on clinical course and arrhythmic
outcome among arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) …

Arrhythmogenic cardiomyopathy (ACM) is an arrhythmogenic disorder of the myocardium
not secondary to ischemic, hypertensive, or valvular heart disease. ACM incorporates a …

Arrhythmogenic cardiomyopathy (AC) is a heart muscle disease clinically characterized by
life-threatening ventricular arrhythmias and pathologically by an acquired and progressive …

Arrhythmogenic cardiomyopathy (ACM) is a rare, heritable heart disease characterized by
fibro-fatty replacement of the myocardium and a high degree of electric instability. It was first …

Cardiac arrhythmias can follow disruption of the normal cellular electrophysiological
processes underlying excitable activity and their tissue propagation as coherent wavefronts …

Arrhythmogenic cardiomyopathy (ACM) is an inherited cardiac disease characterized by
myocardial atrophy, fibro‐fatty replacement, and a high risk of ventricular arrhythmias that …

Aim Arrhythmogenic cardiomyopathy (ACM) is a genetic disorder mainly due to mutations in
desmosomal genes, characterized by progressive fibro-adipose replacement of the …

Aims Arrhythmogenic cardiomyopathy (AC) shows large heterogeneity in its clinical, genetic,
and pathological presentation. This study aims to provide a comprehensive atlas of end …

Arrhythmogenic right ventricular cardiomyopathy (ARVC) is characterized by degeneration
of the right ventricle and ventricular tachycardia originating from the right ventricle …