In this paper the Working Group on Myocardial and Pericardial Disease proposes a revised
definition of dilated cardiomyopathy (DCM) in an attempt to bridge the gap between our …

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 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 characterized by left ventricular dilatation and,
consecutively, contractile dysfunction. The causes of DCM are heterogeneous. DCM often …

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 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 an umbrella term entailing a wide variety of genetic and
non-genetic etiologies, leading to left ventricular systolic dysfunction and dilatation, not …

Objectives. This study sought to determine whether early disease is identifiable in
asymptomatic relatives of patients with dilated cardiomyopathy (DCM) by means of …

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 …

Aim Contemporary survival trends in dilated cardiomyopathy (DCM) are largely unknown.
The aim of this study is to investigate clinical descriptors, survival trends and the prognostic …