Dicarboxylic aminoaciduria: An inborn error of amino acid conservation

This publication has 14 references indexed in Scilit:

• Branched-chain alpha-keto acids isolated as oxime derivatives: Relationship to the corresponding hydroxy acids and amino acids in Maple Syrup Urine Disease
  Metabolism, 1974
• Dicarboxylic aminoaciduria: An inborn error of glutamate and aspartate transport with metabolic implications, in combination with a hyperprolinemia
  Metabolism, 1974
• Use of a "Heparin Lock" in the Intermittent Adminstration of Intravenous Drugs
  Clinical Pediatrics, 1972
• Urinary phenolic acids in tyrosinemia. identification and quantitation by gas chromatographymass spectrometry
  Clinica Chimica Acta; International Journal of Clinical Chemistry, 1971
• Microinjections of L-Leucine into Tubules and Peritubular Capillaries of the Rat
  Nephron, 1971
• A defect in pyruvate decarboxylase in a child with an intermittent movement disorder
  Journal of Clinical Investigation, 1970
• The Renal Clearance of Amino Acids in Cystinuria*
  Journal of Clinical Investigation, 1967
• THE FREE AMINO ACIDS OF HUMAN SPINAL FLUID DETERMINED BY ION EXCHANGE CHROMATOGRAPHY
  Journal of Neurochemistry, 1966
• “Hyperfolic-acidemia with Formiminoglutamic-acjduria Following Histidine Loading”
  The Tohoku Journal of Experimental Medicine, 1963
• Effect of Infusion of Single Amino Acids Upon Excretion of Other Amino Acids
  American Journal of Physiology-Legacy Content, 1951