Dilated cardiomyopathy is conventionally defined as the presence of left ventricular or
biventricular dilatation or systolic dysfunction in the absence of abnormal loading conditions …

There is increasing evidence regarding the prevalence of genetic cardiomyopathies, for
which arrhythmias may be the first presentation. Ventricular and atrial arrhythmias …

Mutations in genes encoding proteins associated with the linker of nucleoskeleton and
cytoskeleton (LINC) complex within the nuclear envelope cause different diseases with …

Genetic cardiomyopathies are disorders of the cardiac muscle, most often explained by
pathogenic mutations in genes encoding sarcomere, cytoskeleton, or ion channel proteins …

There is increasing understanding of the genetic basis to dilated cardiomyopathy and in this
review, we offer a practical primer for the practising clinician. We aim to help all clinicians …

Atrial cardiomyopathy refers to structural and electrical remodelling of the atria, which can
lead to impaired mechanical function. While historical studies have implicated atrial …

In recent years a phenotypic variant of Arrhythmogenic cardiomyopathy has been described,
characterized by predominant left ventricular (LV) involvement with no or minor right …

BACKGROUND: LMNA (lamin A/C)-related dilated cardiomyopathy is a rare genetic cause
of heart failure. In a phase 2 trial and long-term extension, the selective p38αあるふぁ MAPK …

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

Mutations in the LMNA gene (encoding lamin A/C) are a significant cause of familial
arrhythmogenic cardiomyopathy. Although the penetrance is high, there is considerable …