Endomyocardial biopsies for early detection of mitochondrial disorders in hypertrophic cardiomyopathies
- 28 February 1994
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 124 (2) , 224-228
- https://doi.org/10.1016/s0022-3476(94)70308-6
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Mitochondrial Genetics: A Paradigm for Aging and Degenerative Diseases?Science, 1992
- Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR)The Lancet, 1991
- The measurement of the rotenone-sensitive NADH cytochrome c reductase activity in mitochondria isolated from minute amount of human skeletal muscleBiochemical and Biophysical Research Communications, 1990
- Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy.Journal of Clinical Investigation, 1990
- Mapping a Gene for Familial Hypertrophic Cardiomyopathy to Chromosome 14q1New England Journal of Medicine, 1989
- Respiratory chain defects in the mitochondria of cultured skin fibroblasts from three patients with lacticacidemia.Journal of Clinical Investigation, 1986
- Cytochrome c oxidase deficiencyBiochemical Society Transactions, 1985
- Deficiency of the iron-sulfur clusters of mitochondrial reduced nicotinamide-adenine dinucleotide-ubiquinone oxidoreductase (complex I) in an infant with congenital lactic acidosis.Journal of Clinical Investigation, 1984
- Techniques for right and left ventricular endomyocardial biopsyThe American Journal of Cardiology, 1978
- Cardiac structure growth pattern determined by echocardiography.Circulation, 1978