Disruptions in cardiac ion channels have shown to influence the impaired cardiac contraction in heart failure. We sought to determine the altered gene expression profile of this category in dilated cardiomyopathy (DCM) patients and relate the altered gene expression with the clinical signs present in our patients, such as ventricular dysfunction and sustained monomorphic ventricular tachycardia (SMVT).<0.05) in patients with SMVT. up-regulation and the presence of SMVT
Cardiomyopathies represent a wide and heterogeneous group of diseases wherein a genetic cause has be...
AbstractObjectivesWe evaluated the role of Cypher/ZASPin the pathogenesis of dilated cardiomyopathy ...
AbstractWe employed ABI high-density oligonucleotide microarrays containing 31,700 sixty-mer probes ...
Dilated cardiomyopathy (DCM) is characterized by idiopathic dilation and systolic contractile dysfun...
BACKGROUND: Dilated cardiomyopathy (DCM) is characterized by idiopathic dilation and systolic contra...
Dilated cardiomyopathy is characterised by left ventricular dilation that is associated with systoli...
Patients with inherited dilated cardiomyopathy (DCM) frequently die with severe heart failure (HF) o...
Dilated cardiomyopathy (DCM) is a multifactorial disease characterized by left ventricular dilation ...
Ventricular arrhythmias contribute significantly to morbidity and mortality in patients with heart f...
BACKGROUND: Patients with inherited dilated cardiomyopathy (DCM) frequently die with severe heart fa...
Objective: To investigate the global changes accompanying human dilated cardiomyopathy (DCM) we perf...
Dilated cardiomyopathy (DCM) is a major cause of cardiac death and heart transplantation. It has bee...
Objective: To investigate the global changes accompanying human dilated cardiomyopathy (DCM) we perf...
Dilated cardiomyopathy is a heart disease that causes a sudden weakening of the heart muscle in adul...
Dilated cardiomyopathy is a heart disease that causes a sudden weakening of the heart muscle in adul...
Cardiomyopathies represent a wide and heterogeneous group of diseases wherein a genetic cause has be...
AbstractObjectivesWe evaluated the role of Cypher/ZASPin the pathogenesis of dilated cardiomyopathy ...
AbstractWe employed ABI high-density oligonucleotide microarrays containing 31,700 sixty-mer probes ...
Dilated cardiomyopathy (DCM) is characterized by idiopathic dilation and systolic contractile dysfun...
BACKGROUND: Dilated cardiomyopathy (DCM) is characterized by idiopathic dilation and systolic contra...
Dilated cardiomyopathy is characterised by left ventricular dilation that is associated with systoli...
Patients with inherited dilated cardiomyopathy (DCM) frequently die with severe heart failure (HF) o...
Dilated cardiomyopathy (DCM) is a multifactorial disease characterized by left ventricular dilation ...
Ventricular arrhythmias contribute significantly to morbidity and mortality in patients with heart f...
BACKGROUND: Patients with inherited dilated cardiomyopathy (DCM) frequently die with severe heart fa...
Objective: To investigate the global changes accompanying human dilated cardiomyopathy (DCM) we perf...
Dilated cardiomyopathy (DCM) is a major cause of cardiac death and heart transplantation. It has bee...
Objective: To investigate the global changes accompanying human dilated cardiomyopathy (DCM) we perf...
Dilated cardiomyopathy is a heart disease that causes a sudden weakening of the heart muscle in adul...
Dilated cardiomyopathy is a heart disease that causes a sudden weakening of the heart muscle in adul...
Cardiomyopathies represent a wide and heterogeneous group of diseases wherein a genetic cause has be...
AbstractObjectivesWe evaluated the role of Cypher/ZASPin the pathogenesis of dilated cardiomyopathy ...
AbstractWe employed ABI high-density oligonucleotide microarrays containing 31,700 sixty-mer probes ...