Exogenous coenzyme Q (CoQ) fails to increase CoQ in skeletal muscle of two patients with mitochondrial myopathies
- 1 March 1990
- journal article
- research article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 95 (3) , 283-290
- https://doi.org/10.1016/0022-510x(90)90075-x
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Mitochondrial encephalomyopathy (MELAS): Pathological study and successful therapy with coenzyme Q10 and idebenoneJournal of the Neurological Sciences, 1989
- Long‐term coenzyme Q 10 therapy for a mitochondrial encephalomyopathy with cytochrome c oxidase deficiencyNeurology, 1989
- Clinical and biochemical correlations in mitochondrial myopathies treated with coenzyme Q 10Neurology, 1988
- Atypical Form of Menkes Kinky Hair Disease with Mitochondrial NADH-CoQ Reductase DeficiencyNeuropediatrics, 1988
- Mitochondrial Encephalomyopathy with Sleep ApneaEuropean Neurology, 1988
- Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes with recurrent abdominal symptoms and coenzyme Q10 administration.Journal of Neurology, Neurosurgery & Psychiatry, 1987
- Quantitative motor assessment in amyotrophic lateral sclerosisNeurology, 1986
- Treatment of Kearns‐Sayre syndrome with coenzyme Q 10Neurology, 1986
- Decreased activities in mitochondrial inner membrane electron transport system in muscle from patients with Kearns-Sayre syndromeJournal of the Neurological Sciences, 1985
- Improvement of abnormal pyruvate metabolism and cardiac conduction defect with coenzyme Q l0 in Kearns‐Sayre syndromeNeurology, 1985