Carnitine prevents reye-like syndrome in atypical carnitine deficiency
- 30 April 1986
- journal article
- case report
- Published by Elsevier in Pediatric Neurology
- Vol. 2 (2) , 80-84
- https://doi.org/10.1016/0887-8994(86)90061-5
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndromeAnnals of Neurology, 1984
- Renal handling of free and acylcarnitine in secondary carnitine deficiencyNeurology, 1984
- Carnitine metabolism and inborn errorsJournal of Inherited Metabolic Disease, 1984
- Determination of pyruvate dehydrogenase in cultured human fibroblasts and amniotic fluid cellsClinica Chimica Acta; International Journal of Clinical Chemistry, 1982
- Systemic Carnitine Deficiency — A Treatable Inherited Lipid-Storage Disease Presenting as Reye's SyndromeNew England Journal of Medicine, 1980
- Successful carnitine treatment in a non-carnitine-deficient lipid storage myopathyEuropean Journal of Pediatrics, 1980
- The Syndrome of Carnitine Deficiency: Morphological and Metabolic Correlations in Two CasesCanadian Journal of Neurological Sciences, 1978
- The syndrome of systemic carnitine deficiencyNeurology, 1975
- Studies on Cytochrome a: XV. Cytochrome Oxidase Activity of the Okunuki Preparation and Its Activation by Heat, Alkali and Detergent Treatments*The Journal of Biochemistry, 1965
- [131] Cytochrome b (mammals)Published by Elsevier ,1955