Desmoplakin (DSP) is a desmosomal protein that plays an essential role for cell-to-cell
adhesion within the cardiomyocytes. The first association between DSP genetic variants and …

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

Sudden cardiac death (SCD) prevention in cardiomyopathies such as hypertrophic (HCM),
dilated (DCM), non-dilated left ventricular (NDLCM), and arrhythmogenic right ventricular …

Prolonged and intensive exercise induces remodeling of all four cardiac chambers, a
physiological process which is coined as the “athlete's heart”. This cardiac adaptation …

Dilated cardiomyopathy (DCM) represents one of the most common causes of non-ischemic
heart failure, characterised by ventricular dilation alongside systolic dysfunction. Despite …

Arrhythmogenic cardiomyopathy (ACM) is a genetic heart muscle disease, structurally
characterized by progressive fibro‐fatty replacement of the normal myocardium and …

Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited disease
characterized by the progressive replacement of the normal myocardium by fibroadipocytic …

Arrhythmogenic cardiomyopathy (ACM) is a genetic disease characterized by replacement
of ventricular myocardium with fibrofatty tissue, predisposing the patient to ventricular …

Arrhythmogenic cardiomyopathy (ACM) is a heart disease characterized by a fibrotic
replacement of myocardial tissue and a consequent predisposition to ventricular arrhythmic …

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 …