Serum and urinary carnitine and organic acids in reye syndrome and Reye-like syndrome
Authors:
- 1 January 1986
- journal article
- research article
- Published by Elsevier in Brain and Development
- Vol. 8 (3) , 257-261
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Urinary dicarboxylic acids in Reye syndromeThe Journal of Pediatrics, 1985
- L-carnitine enhances excretion of propionyl coenzyme A as propionylcarnitine in propionic acidemia.Journal of Clinical Investigation, 1984
- Propionylcarnitine excretion in propionic and methylmalonic acidurias: a cause of carnitine deficiencyClinica Chimica Acta, 1984
- Application of high resolution fast atom bombardment and constant B/E ratio linked scanning to the identification and analysis of acylcarnitines in metabolic diseaseJournal of Mass Spectrometry, 1984
- HYPOCARNITINAEMIA IN DISORDERS OF ORGANIC ACID METABOLISMThe Lancet, 1982
- Systemic Carnitine Deficiency — A Treatable Inherited Lipid-Storage Disease Presenting as Reye's SyndromeNew England Journal of Medicine, 1980
- Serum Carnitine in Reye's SyndromeNew England Journal of Medicine, 1980
- Systemic carnitine deficiency simulating recurrent Reye syndromeThe Journal of Pediatrics, 1980
- Tissue carnitine in reye syndromeAnnals of Neurology, 1978
- ENCEPHALOPATHY AND FATTY DEGENERATION OF THE VISCERA A DISEASE ENTITY IN CHILDHOODThe Lancet, 1963