Results 231 to 240 of about 69,694 (262)
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Arrhythmias in Dilated Cardiomyopathy

Cardiac Electrophysiology Clinics, 2015
Patients with dilated cardiomyopathies (DCM) face a significant burden of arrhythmias, including conduction defects such as atrioventricular block and interventricular delay in the form of left bundle branch block, resulting in altered electromechanical coupling that can exacerbate heart failure.
Saurabh, Kumar   +2 more
openaire   +2 more sources

Dilated cardiomyopathy: an update

Veterinary Clinics of North America: Small Animal Practice, 2004
Despite many advances in he diagnosis and treatment of DCM, it continues to be an important cause of cardiovascular morbidity and mortality in large-breed dogs. In the coming years, it is hoped and anticipated tht further discoveries will be made in the areas of etiology, therapy, and assessment of prognosis, ultimately with a view to having a greater ...
Michael R, O'Grady, M Lynne, O'Sullivan
openaire   +2 more sources

Pharmacotherapy of Dilated Cardiomyopathy

Current Pharmaceutical Design, 2014
The pharmacological treatment of dilated cardiomyopathy overlaps with the treatment of heart failure. The primary objective of this treatment is to slow the progression of disease and improve quality and length of life. All patients, including those with asymptomatic dysfunction of the left ventricle, ought to receive angiotensin converting enzyme ...
Lenka, Spinarova, Jindrich, Spinar
openaire   +2 more sources

Immunosuppression for Dilated Cardiomyopathy

New England Journal of Medicine, 1989
The diagnosis of dilated cardiomyopathy is made when left ventricular dilatation and systolic dysfunction, with normal wall thickness, occur in the absence of coronary artery, valvular, or pericardial disease.1 The right ventricle is also often involved.
openaire   +2 more sources

[Etiopathogenesis of dilated cardiomyopathies].

Cardiologia (Rome, Italy), 1993
This study was carried out on 43 patients affected by dilated cardiomyopathy to investigate some of the etiopathological hypotheses on this illness. The Authors investigated: the persistence of virus genoma (coxsackie, HBV) on endomyocardial biopsies; the pattern of the II class major histocompatibility complex (MHC) were in the blood lymphocytes; the ...
PETRONIO, ANNA   +7 more
openaire   +2 more sources

Dilated cardiomyopathy: causes, mechanisms, and current and future treatment approaches

Lancet, The, 2023
Carsten Tschope   +2 more
exaly  

Rare Variant Genetics and Dilated Cardiomyopathy Severity: The DCM Precision Medicine Study

Circulation, 2023
Ray E Hershberger   +2 more
exaly  

The genetics of dilated cardiomyopathy

Heart Rhythm, 2012
English, Flack, Prince J, Kannankeril
openaire   +2 more sources

The Frequency of Familial Dilated Cardiomyopathy in a Series of Patients with Idiopathic Dilated Cardiomyopathy

New England Journal of Medicine, 1992
Henry Tazelaar   +2 more
exaly  

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