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30Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiency, Journal of Inherited Metabolic Disease Biochemical studies in a patient with defects in the metabolism of acyl-CoA and sarcosine: Another possible case of glutaric aciduria type II, Journal of Inherited Metabolic Disease Possible deleterious effect ofL-carnitine supplementation in a patient with mild multiple acyl-CoA dehydrogenation deficiency (ethylmalonic-adipic aciduria), Journal of Inherited Metabolic Disease The occurrence of C6u2013C10-dicarboxylic acids, ethylmalonic acid, 5-hydroxycaproic acid, butyrylglycine, isovalerylglycine, isobutyrylglycine, 2-methylbutyrylglycine and glutaric acid in the urine of riboflavin deficient rats, Journal of Inherited Metabolic Disease A new patient with dicarboxylic aciduria suggestive of medium-chain acyl-CoA dehydrogenase deficiency presenting as Reye's syndrome, Journal of Inherited Metabolic Disease Generalised Dicarboxylic Aciduria: A Common Finding in Neonates, Journal of Inherited Metabolic Disease Gas Chromatographyu2014Mass Spectrometry (GCu2014MS) Diagnosis of Two Cases of Medium Chain Acyl-CoA Dehydrogenase Deficiency, Organic Acidurias Generalised Dicarboxylic Aciduria: A Common Finding in Neonates, Studies in Inherited Metabolic Disease Gas chromatography-mass spectrometry (GC-MS) diagnosis of two cases of medium chain Acyl-CoA dehydrogenase deficiency, Journal of Inherited Metabolic Disease