Impaired mitochondrial function in idiopathic dilated cardiomyopathy: Biochemical and molecular analysis
- 1 September 1995
- journal article
- research article
- Published by Elsevier in Journal of Cardiac Failure
- Vol. 1 (4) , 285-291
- https://doi.org/10.1016/1071-9164(95)90003-9
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Cardiomyopathy and abnormal mitochondrial functionCardiovascular Research, 1994
- Mitochondrial DNA deletions in dilated cardiomyopathy: A clinical study employing endomyocardial samplingJournal of the American College of Cardiology, 1994
- Endomyocardial biopsies for early detection of mitochondrial disorders in hypertrophic cardiomyopathiesThe Journal of Pediatrics, 1994
- Accumulation of deletions in human mitochondrial DNA during normal aging: analysis by quantitative PCRBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1992
- Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNAThe Lancet, 1992
- Age-dependent increase in deleted mitochondrial DNA in the human heart: Possible contributory factor to presbycardiaAmerican Heart Journal, 1991
- Mitochondrial mutation in fatal infantile cardiomyopathyThe Lancet, 1990
- Multiple mitochondrial DNA deletions exist in cardiomyocytes of patients with hypertrophic or dilated cardiomyopathyBiochemical and Biophysical Research Communications, 1990
- Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre SyndromeNew England Journal of Medicine, 1989
- Some biochemical studies on subcellular systems isolated from fresh recipient human cardiac tissue obtained during transplantationThe American Journal of Cardiology, 1971