Quantitative analysis of urinary acylglycines for the diagnosis of β-oxidation defects using GC-NCI-MS

This publication has 19 references indexed in Scilit:

• 3-, 6- and 7-Hydroxyoctanoic Acids are Metabolites of Medium-Chain Triglycerides and Excreted in Urine as Glucuronides
  Journal of Mass Spectrometry, 1996
• Clinical and biochemical characterization of short-chain acyl-coenzyme A dehydrogenase deficiency
  The Journal of Pediatrics, 1995
• Population Screening for Medium-Chain Acyl-CoA Dehydrogenase Deficiency: Analysis of Medium-Chain Fatty Acids and Acylglyeines in Blood Spots
  Annals of Clinical Biochemistry: International Journal of Laboratory Medicine, 1994
• Tandem mass spectrometry: A new method for acylcarnitine profiling with potential for neonatal screening for inborn errors of metabolism
  Journal of Inherited Metabolic Disease, 1990
• Medium-Chain Acyl-CoA Dehydrogenase Deficiency
  New England Journal of Medicine, 1988
• Pulse oximetry for continuous oxygen monitoring in sick newborn infants
  The Journal of Pediatrics, 1986
• Acyl-CoA: Glycine N-acyltransferase: Organelle localization and affinity toward straight-and branched-chained acyl-CoA esters in rat liver
  Biochemical Medicine and Metabolic Biology, 1986
• A SIMPLE SCREENING TEST FOR MEDIUM-CHAIN ACYL CoA DEHYDROGENASE DEFICIENCY
  The Lancet, 1986
• Suberylglycine excretion in the urine from a patient with dicarboxylic aciduria
  Clinica Chimica Acta, 1976
• The specificity of glycine-N-acylase and acylglycine excretion in the organicacidaemias
  Biochemical Medicine, 1974