Dilated cardiomyopathy (DCM) is a clinical diagnosis characterized by left ventricular or
biventricular dilation and impaired contraction that is not explained by abnormal loading …

Dilated cardiomyopathy (DCM) is characterized by left ventricular dilatation and,
consecutively, contractile dysfunction. The causes of DCM are heterogeneous. DCM often …

Despite recent advances in the management of patients with heart failure, morbidity and
mortality rates remain high. Common causes of heart failure are ischaemic heart disease …

Dilated cardiomyopathy (DCM) is an important cause of sudden cardiac death (SCD) and
heart failure (HF) and is the leading indication for cardiac transplantation in children and …

Dilated cardiomyopathy (DCM) is a common cardiac diagnosis that may result as a
consequence of a variety of pathologies. The differential diagnosis remains quite broad …

Dilated cardiomyopathy (DCM) is an umbrella term entailing a wide variety of genetic and
non-genetic etiologies, leading to left ventricular systolic dysfunction and dilatation, not …

Dilated cardiomyopathy (DCM) represents a particular aetiology of systolic heart failure that
frequently has a genetic background and usually affects young patients with few co …

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

Dilated cardiomyopathy (DCM) is best understood as the final common response of
myocardium to diverse genetic and environmental insults. A rigorous work-up can exclude …

Dilated cardiomyopathy is defined by the presence of left ventricular dilatation and
contractile dysfunction. Genetic mutations involving genes that encode cytoskeletal …