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. 1969 Apr;44(234):152–161. doi: 10.1136/adc.44.234.152

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

B Levin, J M Abraham, V G Oberholzer, E A Burgess
PMCID: PMC2020046  PMID: 5779426

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. ALLAN J. D., CUSWORTH D. C., DENT C. E., WILSON V. K. 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. doi: 10.1016/s0140-6736(58)90666-4. [DOI] [PubMed] [Google Scholar]
  2. BROWN G. W., Jr, COHEN P. P. 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] [Google Scholar]
  3. Bürgi W., Richterich R., Colombo J. P. L-Lysine dehydrogenase deficiency in a patient with congenital lysine intolerance. Nature. 1966 Aug 20;211(5051):854–855. doi: 10.1038/211854a0. [DOI] [PubMed] [Google Scholar]
  4. FENTON J. C. The estimation of plasma ammonia by ion exchange. Clin Chim Acta. 1962 Mar;7:163–175. doi: 10.1016/0009-8981(62)90004-9. [DOI] [PubMed] [Google Scholar]
  5. LEVIN B., MACKAY H. M., OBERHOLZER V. G. Argininosuccinic aciduria, an inborn error of amino acid metabolism. Arch Dis Child. 1961 Dec;36:622–632. doi: 10.1136/adc.36.190.622. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Levin B. Arginosuccine aciduria. Am J Dis Child. 1967 Jan;113(1):162–165. [PubMed] [Google Scholar]
  7. Levin B., Dobbs R. H., Burgess E. A., Palmer T. Hyperammonaemia. A variant type of deficiency of liver ornithine transcarbamylase. Arch Dis Child. 1969 Apr;44(234):162–169. doi: 10.1136/adc.44.234.162. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Levin B., Russell A. Treatment of hyperammonemia. Am J Dis Child. 1967 Jan;113(1):142–145. doi: 10.1001/archpedi.1967.02090160192031. [DOI] [PubMed] [Google Scholar]
  9. MCMURRAY W. C., RATHBUN J. C., MOHYUDDIN F., KOEGLER S. J. CITRULLINURIA. Pediatrics. 1963 Sep;32:347–357. [PubMed] [Google Scholar]
  10. PEONIDES A., LEVIN B., YOUNG W. F. THE RENAL EXCRETION OF HYDROGEN IONS IN INFANTS AND CHILDREN. Arch Dis Child. 1965 Feb;40:33–39. doi: 10.1136/adc.40.209.33. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Perheentupa J., Visakorpi J. K. Protein intolerance with deficient transport of basic aminoacids. Another inborn error of metabolism. Lancet. 1965 Oct 23;2(7417):813–816. doi: 10.1016/s0140-6736(65)92446-3. [DOI] [PubMed] [Google Scholar]
  12. RINDERKNECHT H., RINDERKNECHT J. F. 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] [Google Scholar]
  13. RUSSELL A., LEVIN B., OBERHOLZER V. G., SINCLAIR L. Hyperammonaemia. A new instance of an inborn enzymatic defect of the biosynthesis of urea. Lancet. 1962 Oct 6;2(7258):699–700. doi: 10.1016/s0140-6736(62)90508-1. [DOI] [PubMed] [Google Scholar]
  14. STEIN W. H., MOORE S. The free amino acids of human blood plasma. J Biol Chem. 1954 Dec;211(2):915–926. [PubMed] [Google Scholar]

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