Skip to main content
Archives of Disease in Childhood logoLink to Archives of Disease in Childhood
. 1969 Dec;44(238):681–687. doi: 10.1136/adc.44.238.681

Periodic attacks of lethargy in a baby with ammonia intoxication due to a congenital defect in ureogenesis.

L M Corbeel, J P Colombo, M Van Sande, A Weber
PMCID: PMC2020339  PMID: 5356973

Full text

PDF
681

Selected References

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

  1. 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]
  2. Colombo J. P., Ungari S., Ferrazzini F., Richterich R., Rossi E. Periodischer Stupor und Ammoniakintoxikation bei einem Kind mit anikterischer, subakuter Hepatitis. Helv Paediatr Acta. 1967 Aug;22(4):331–341. [PubMed] [Google Scholar]
  3. DUDA G. D., HANDLER P. Kinetics of ammonia metabolism in vivo. J Biol Chem. 1958 May;232(1):303–314. [PubMed] [Google Scholar]
  4. Levin B., Abraham J. M., Oberholzer V. G., Burgess E. A. Hyperammonaemia: a deficiency of liver ornithine transcarbamylase. Occurrence in mother and child. Arch Dis Child. 1969 Apr;44(234):152–161. doi: 10.1136/adc.44.234.152. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. 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]
  6. 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]
  7. Rogers L. E., Porter F. S. Hereditary orotic aciduria. II. A urinary screening test. Pediatrics. 1968 Sep;42(3):423–428. [PubMed] [Google Scholar]
  8. SCHIMKE R. T. Adaptive characteristics of urea cycle enzymes in the rat. J Biol Chem. 1962 Feb;237:459–468. [PubMed] [Google Scholar]
  9. SELIGSON D., HIRAHARA K. The measurement of ammonia in whole blood, erythrocytes, and plasma. J Lab Clin Med. 1957 Jun;49(6):962–974. [PubMed] [Google Scholar]
  10. TOMLINSON S., WESTALL R. G. ARGININOSUCCINIC ACIDURIA. ARGININOSUCCINASE AND ARGINASE IN HUMAN BLOOD CELLS. Clin Sci. 1964 Apr;26:261–269. [PubMed] [Google Scholar]
  11. Tedesco T. A., Mellman W. J. Argininosuccinate synthetase activity and citrulline metabolism in cells cultured from a citrullinemic subject. Proc Natl Acad Sci U S A. 1967 Mar;57(3):829–834. doi: 10.1073/pnas.57.3.829. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. WEBER H. [A micromethod for determining ornithine carbamoyltransferase (OCT) in blood and cerebrospinal fluid]. Klin Wochenschr. 1963 Jan 1;41:37–40. doi: 10.1007/BF01478619. [DOI] [PubMed] [Google Scholar]

Articles from Archives of Disease in Childhood are provided here courtesy of BMJ Publishing Group

RESOURCES