Medium chain acyl CoA dehydrogenase deficiency
- 31 August 1991
- journal article
- editorial
- Published by Elsevier in The Lancet
- Vol. 338 (8766) , 544-545
- https://doi.org/10.1016/0140-6736(91)91105-4
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
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- Frequency of the G985 MCAD mutation in the general populationThe Lancet, 1991
- Mutations in medium chain acyl-CoA dehydrogenase deficiencyThe Lancet, 1990
- Diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiency in the neonatal period by measurement of medium-chain fatty acids in plasma and filter paper blood samplesThe Journal of Pediatrics, 1990
- Medium-chain acyl-CoA dehydrogenase deficiency: a useful diagnosis five years after deathClinical Chemistry, 1990
- Tandem mass spectrometry: A new method for acylcarnitine profiling with potential for neonatal screening for inborn errors of metabolismJournal of Inherited Metabolic Disease, 1990
- Cis-4-decenoic acid in plasma: a characteristic metabolite in medium-chain acyl-CoA dehydrogenase deficiency.Clinical Chemistry, 1988
- Purification and characterization of short-chain, medium-chain, and long-chain acyl-CoA dehydrogenases from rat liver mitochondria. Isolation of the holo- and apoenzymes and conversion of the apoenzyme to the holoenzyme.Journal of Biological Chemistry, 1985
- General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three casesClinica Chimica Acta; International Journal of Clinical Chemistry, 1983