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12Biochemical 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 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 The Diagnosis and Treatment of a Patient with Medium-chain Acyl-CoA Dehydrogenase Deficiency: Overnight Fasting Does Not Result in the Expected Urinary Metabolite Profile, Practical Developments in Inherited Metabolic Disease: DNA Analysis, Phenylketonuria and Screening for Congenital Adrenal Hyperplasia Vitreous humour organic acids in medium chain acyl-CoA dehydrogenase deficiency, Journal of Inherited Metabolic Disease The diagnosis and treatment of a patient with medium-chain acyl-CoA dehydrogenase deficiency: Overnight fasting does not result in the expected urinary meta10545te profile, 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 Gas Chromatographyu2014Mass Spectrometry (GCu2014MS) Diagnosis of Two Cases of Medium Chain Acyl-CoA Dehydrogenase Deficiency, Organic Acidurias Gas chromatography-mass spectrometry (GC-MS) diagnosis of two cases of medium chain Acyl-CoA dehydrogenase deficiency, Journal of Inherited Metabolic Disease Riboflavin-responsive ethylmalonicu2014adipic aciduria, Journal of Inherited Metabolic Disease Adult presentation of MCAD deficiency revealed by coma and severe arrythmias., Intensive Care Medicine