An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes
- 1 December 1983
- journal article
- research article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 62 (1-3) , 327-355
- https://doi.org/10.1016/0022-510x(83)90209-5
Abstract
No abstract availableThis publication has 33 references indexed in Scilit:
- Systemic Carnitine Deficiency Presenting as Familial Endocardial FibroelastosisNew England Journal of Medicine, 1981
- Variation in plasma ketone bodies during a 24-hour fast in normal and in hypoglycemic children: Relationship to ageThe Journal of Pediatrics, 1981
- Multisystem triglyceride storage disorder with impaired long‐chain fatty acid oxidationAnnals of Neurology, 1980
- Glucagon treatment stimulates the oxidation of durohydroquinone by rat liver mitochondriaFEBS Letters, 1979
- Systemic carnitine deficiencyThe Journal of Pediatrics, 1978
- Cardiac biopsy in skeletal myopathy: Report of a case with myocardial mitochondrial abnormalitiesThe Journal of Pathology, 1976
- Congenital cataract and mitochondrial myopathy of skeletal and heart muscle associated with lactic acidosis after exerciseThe Journal of Pediatrics, 1975
- The quantitative estimation of cytochrome b in sub-mitochondrial particles from beef heartBiochemical and Biophysical Research Communications, 1962
- The extinction coefficient of cytochrome cBiochimica et Biophysica Acta, 1962
- Enzymic Activities of Human Skeletal Muscle Mitochondria: A Tool in Clinical Metabolic ResearchNature, 1959