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Immunoadsorption in Dilated Cardiomyopathy
2006Dilated cardiomyopathy (DCM) is characterized by progressive reduction in contractile function and by dilatation of the right and left ventricles. Abnormalities of the cellular and humoral immune system are present in patients with myocarditis and DCM. Several antibodies against cardiac structures have been detected in DCM patients.
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Immunopathogenesis of dilated cardiomyopathies
Current Opinion in Cardiology, 1995Idiopathic dilated cardiomyopathy is a chronic heart muscle disorder of unknown etiology, but experimental and clinical evidence is accumulating that points to an immune pathogenesis in a subset of patients, and to the potential importance of myosin as an antigen. Most recent developments include evidence of cardiac- and disease-specific autoantibodies
J H, Goldman, W J, McKenna
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Genetics of dilated cardiomyopathy
2000Dilated cardiomyopathy (DCM) is a heart muscle disorder characterized by cardiac dilatation and impaired systolic function. In an increasing number of all DCM cases a specific etiology can be identified and in the remaining patients DCM is termed idiopathic. There is a wide variation of the clinical presentation in DCM.
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Rare Variant Genetics and Dilated Cardiomyopathy Severity: The DCM Precision Medicine Study
Circulation, 2023Ray E Hershberger +2 more
exaly
The genetics of dilated cardiomyopathy
Heart Rhythm, 2012English, Flack, Prince J, Kannankeril
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Genotype and Cardiac Outcomes in Pediatric Dilated Cardiomyopathy
Journal of the American Heart Association, 2022Alexander InG +2 more
exaly
Understanding the genetics of adult-onset dilated cardiomyopathy: what a clinician needs to know
European Heart Journal, 2021Neal K Lakdawala +2 more
exaly
Familial dilated cardiomyopathy
The American Journal of Cardiology, 1984E G, Voss +5 more
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