Criteria for diagnosis of arrhythmogenic cardiomyopathy (ACM) were first proposed in 1994
and revised in 2010 by a Task Force. Although the Task Force criteria demonstrated a good …

Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare, heritable myocardial
disease associated with the development of ventricular arrhythmias, heart failure, and …

Arrhythmogenic cardiomyopathy (ACM) is a heart muscle disease characterized by
prominent “non-ischemic” myocardial scarring predisposing to ventricular electrical …

Arrhythmogenic cardiomyopathy (ACM) is a genetically determined heart muscle disease
characterized by fibro-fatty myocardial replacement, clinically associated with malignant …

Arrhythmogenic Cardiomyopathy (ACM) is a heredo-familial cardiac disease characterized
by fibro-fatty myocardial replacement and increased risk of sudden cardiac death. The …

Cardiomyopathies are a heterogeneous group of structural, mechanical, and electrical heart
muscle disorders which often correlate with life-threatening arrhythmias and progressive …

Objectives The present study aimed to investigate the incremental prognostic value of the
right ventricular fractal dimension (FD), a novel marker of myocardial trabecular complexity …

Arrhythmogenic cardiomyopathy (ACM) is a rare heart muscle disease characterized by a
progressive fibro-fatty myocardial replacement, ventricular arrhythmias, and increased risk of …

Arrhythmogenic Cardiomyopathy (ACM) is a cardiac disorder characterized by non-ischemic
myocardial scarring, which may lead to ventricular electrical instability and systolic …

Arrhythmogenic cardiomyopathy (ACM) is a cardiac disease featured by non-ischemic
myocardial scarring linked to ventricular electrical instability. As there is no single gold …