Idiopathic dilated cardiomyopathy (IDCM) is a primary myocardial disease of unknown cause characterized by ventricular chamber enlargement with impaired contractile function. In familial forms of IDCM, mutations of genes coding for cytoskeletal proteins related to force transmission, such as dystrophin, cardiac actin, desmin, and delta-sarcoglycan, have been identified. Here, we report the data of a retrospective investigation carried out to evaluate the expression of atrial natriuretic peptide (ANP), CD34, troponin T and nestin in the myocardium of patients affected with IDCM. Formalin-fixed and paraffin-embedded consecutive tissue sections from the ventricular wall of 10 human normal hearts (NH) following forensic autopsy and 22 IDCM (liv...
Objective: To investigate the global changes accompanying human dilated cardiomyopathy (DCM) we perf...
Cardiac autoantibodies play a pathogenic role in dilated cardiomyopathy (DCM). Removal of antibodies...
Background and aims Myotonic dystrophy type 1 (DM1) and type 2 (DM2) are dominant inherited muscular...
Idiopathic dilated cardiomyopathy (IDCM) is a primary myocardial disease of unknown cause characteri...
Objectives.This study was designed to determine whether atrial natriuretic peptide and skeletal alph...
Nitric oxide is known to exert negative inotropic effects on myocytes. Initial reports using activit...
RATIONALE: Idiopathic dilated cardiomyopathy (DCM) is inherited in approximately one third of cases,...
Key points: Mutations in genes encoding cardiac troponin I (TNNI3) and cardiac troponin T (TNNT2) ca...
Rationale: Idiopathic dilated cardiomyopathy (DCM) is inherited in approximately one third of cases,...
Dilated cardiomyopathy (DCM), a leading cause of heart failure and heart transplantation in younger ...
BACKGROUND AND AIMS: While the molecular basis of dilated cardiomyopathy (DCM) remains uncertain, co...
AbstractObjectives. We examined the mRNA expression and protein localization of inducible nitric oxi...
Objective: To investigate the global changes accompanying human dilated cardiomyopathy (DCM) we perf...
Background: We investigated changes in genetic expression of atrial and brain natriuretic peptides (...
<div><p>Background</p><p>The atrium is the major site of ANP synthesis, which has been said to incre...
Objective: To investigate the global changes accompanying human dilated cardiomyopathy (DCM) we perf...
Cardiac autoantibodies play a pathogenic role in dilated cardiomyopathy (DCM). Removal of antibodies...
Background and aims Myotonic dystrophy type 1 (DM1) and type 2 (DM2) are dominant inherited muscular...
Idiopathic dilated cardiomyopathy (IDCM) is a primary myocardial disease of unknown cause characteri...
Objectives.This study was designed to determine whether atrial natriuretic peptide and skeletal alph...
Nitric oxide is known to exert negative inotropic effects on myocytes. Initial reports using activit...
RATIONALE: Idiopathic dilated cardiomyopathy (DCM) is inherited in approximately one third of cases,...
Key points: Mutations in genes encoding cardiac troponin I (TNNI3) and cardiac troponin T (TNNT2) ca...
Rationale: Idiopathic dilated cardiomyopathy (DCM) is inherited in approximately one third of cases,...
Dilated cardiomyopathy (DCM), a leading cause of heart failure and heart transplantation in younger ...
BACKGROUND AND AIMS: While the molecular basis of dilated cardiomyopathy (DCM) remains uncertain, co...
AbstractObjectives. We examined the mRNA expression and protein localization of inducible nitric oxi...
Objective: To investigate the global changes accompanying human dilated cardiomyopathy (DCM) we perf...
Background: We investigated changes in genetic expression of atrial and brain natriuretic peptides (...
<div><p>Background</p><p>The atrium is the major site of ANP synthesis, which has been said to incre...
Objective: To investigate the global changes accompanying human dilated cardiomyopathy (DCM) we perf...
Cardiac autoantibodies play a pathogenic role in dilated cardiomyopathy (DCM). Removal of antibodies...
Background and aims Myotonic dystrophy type 1 (DM1) and type 2 (DM2) are dominant inherited muscular...