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15Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiency, Journal of Inherited Metabolic Disease Medium-chain acyl-CoA dehydrogenase deficiency does not correlate with apparent life-threatening events and the sudden infant death syndrome: results from phenylpropionate loading tests and DNA analysis, European Journal of Pediatrics Early diagnosis and treatment of neonatal medium-chain acyl-CoA dehydrogenase deficiency: Report of two siblings, European Journal of Pediatrics 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 Use of Phenylpropionic Acid as a Loading Test for Medium-Chain Acyl-CoA Dehydrogenase Deficiency, Studies in Inherited Metabolic Disease The use of phenylpropionic acid as a loading test for medium-chain acyl-CoA dehydrogenase deficiency, Journal of Inherited Metabolic Disease Comparison of Urinary Acylglycines and Acylcarnitines as Diagnostic Markers of Medium-chain Acyl-CoA Dehydrogenase Deficiency, Studies in Inherited Metabolic Disease