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Arch Dis Child. 1969 April; 44(234): 152–161.
PMCID: PMC2020046

Hyperammonaemia: a deficiency of liver ornithine transcarbamylase. Occurrence in mother and child.

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Selected References

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  • ALLAN JD, CUSWORTH DC, DENT CE, WILSON VK. A disease, probably hereditary characterised by severe mental deficiency and a constant gross abnormality of aminoacid metabolism. Lancet. 1958 Jan 25;1(7013):182–187. [PubMed]
  • BROWN GW, Jr, COHEN PP. Comparative biochemistry of urea synthesis. I. Methods for the quantitative assay of urea cycle enzymes in liver. J Biol Chem. 1959 Jul;234(7):1769–1774. [PubMed]
  • Bürgi W, Richterich R, Colombo JP. L-Lysine dehydrogenase deficiency in a patient with congenital lysine intolerance. Nature. 1966 Aug 20;211(5051):854–855. [PubMed]
  • FENTON JC. The estimation of plasma ammonia by ion exchange. Clin Chim Acta. 1962 Mar;7:163–175. [PubMed]
  • Levin B. Arginosuccine aciduria. Am J Dis Child. 1967 Jan;113(1):162–165. [PubMed]
  • Levin B, Dobbs RH, Burgess EA, Palmer T. Hyperammonaemia. A variant type of deficiency of liver ornithine transcarbamylase. Arch Dis Child. 1969 Apr;44(234):162–169. [PMC free article] [PubMed]
  • LEVIN B, MACKAY HM, OBERHOLZER VG. Argininosuccinic aciduria, an inborn error of amino acid metabolism. Arch Dis Child. 1961 Dec;36:622–632. [PMC free article] [PubMed]
  • Levin B, Russell A. Treatment of hyperammonemia. Am J Dis Child. 1967 Jan;113(1):142–145. [PubMed]
  • MCMURRAY WC, RATHBUN JC, MOHYUDDIN F, KOEGLER SJ. CITRULLINURIA. Pediatrics. 1963 Sep;32:347–357. [PubMed]
  • PEONIDES A, LEVIN B, YOUNG WF. THE RENAL EXCRETION OF HYDROGEN IONS IN INFANTS AND CHILDREN. Arch Dis Child. 1965 Feb;40:33–39. [PMC free article] [PubMed]
  • Perheentupa J, Visakorpi JK. Protein intolerance with deficient transport of basic aminoacids. Another inborn error of metabolism. Lancet. 1965 Oct 23;2(7417):813–816. [PubMed]
  • RINDERKNECHT H, RINDERKNECHT JF. A SIMPLE METHOD FOR THE QUANTITATIVE DETERMINATION OF URINARY PSEUDOURIDINE AND SOME NEW ULTRAVIOLET-ABSORBING METABOLITES. J Lab Clin Med. 1965 Jun;65:1034–1040. [PubMed]
  • RUSSELL A, LEVIN B, OBERHOLZER VG, SINCLAIR L. Hyperammonaemia. A new instance of an inborn enzymatic defect of the biosynthesis of urea. Lancet. 1962 Oct 6;2(7258):699–700. [PubMed]
  • STEIN WH, MOORE S. The free amino acids of human blood plasma. J Biol Chem. 1954 Dec;211(2):915–926. [PubMed]

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