Background β blockers reduce mortality in patients who have chronic heart failure, systolic
dysfunction, and are on background treatment with diuretics and angiotensin-converting …

Background Dilated cardiomyopathy and hypertrophic cardiomyopathy arise from mutations
in many genes. TTN, the gene encoding the sarcomere protein titin, has been insufficiently …

Aspirin and P2Y 12 receptor antagonists are widely used across the spectrum of cardiovascular
and cerebrovascular diseases. Gastrointestinal complications, including ulcer and …

Objectives : We evaluated the role of Cypher/ZASPin the pathogenesis of dilated cardiomyopathy
(DCM) with or without isolated non-compaction of the left ventricular myocardium (…

Objectives : We examined the prevalence, genotype-phenotype correlation, and natural
history of lamin A/C gene (LMNA) mutations in subjects with dilated cardiomyopathy (DCM). …

Objectives. This study was undertaken to evaluate the frequency of restrictive left ventricular
filling pattern in dilated cardiomyopathy, as well as its clinical and hemodynamic …

OBJECTIVES This study was performed to evaluate the characteristics, mode of inheritance
and etiology of familial dilated cardiomyopathy (FDC). BACKGROUND A genetic form of …

Objectives : The purpose of this study was to determine the prevalence and prognostic role
of left ventricular reverse remodeling (LVRR) in idiopathic dilated cardiomyopathy (IDCM). …

The coronavirus disease 2019 (COVID-19), a deadly pandemic that has affected millions of
people worldwide, is associated with cardiovascular complications, including venous and …

To clarify the clinical and prognostic value of the ECG, an ECG review was undertaken in 45
consecutive patients with a histologic diagnosis of active myocarditis (29 men and boys and …