Evolution of dilated cardiomyopathy (DCM) from idiopathic hypertrophic cardiomyopathy (IHCM) vs. inflammatory dilated cardiomyopathy (DCMi): a rare case of sudden death in an 8-year-old boy by R. Dettmeyer, P. Schmidt, R. Kandolf and B. Madea, Pathol. Res. Pract. 200 (2004) 411

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Evolution of dilated cardiomyopathy (DCM) from idiopathic hypertrophic cardiomyopathy (IHCM) vs. inflammatory dilated cardiomyopathy (DCMi): a rare case of sudden death in an 8-year-old boy by R. Dettmeyer, P. Schmidt, R. Kandolf and B. Madea, Pathol. Res. Pract. 200 (2004) 411–415

Published:2004-06 Issue:5 Volume:200 Page:417-421
ISSN:0344-0338
Container-title:Pathology - Research and Practice
language:en
Short-container-title:Pathology - Research and Practice

Author:

Hort W,Schwartzkopff B

Publisher

Elsevier BV

Subject

Cell Biology,Pathology and Forensic Medicine

Reference29 articles.

1. Coexistence of mitochondrial DNA and beta myosin heavy chain mutations in hypertrophic cardiomyopathy with late congestive heart failure;Arbustini;Heart,1998

2. Pathology of cardiomyopathies;Becker,1998

3. Ischemic cardiomyopathy lack of clinical applicability of the WHO/ISFC classification of cardiomyopathies;Boffa;Ital. Heart J.,2001

4. Report of the WHO/ISFC task force on the definition and classification of cardiomyopathies;Brandenburg;Br. Heart J.,1980

5. Idiopathic myocardial hypertrophy without congestive heart failure or obstruction to blood flow;Braunwald;Am. J. Med.,1963

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