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Arch Dis Child. 1969 April; 44(234): 143–148.
PMCID: PMC2020044

Hyperammonaemia Due to Ornithine Transcarbamylase Deficiency

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Selected References

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  • 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]
  • RICHTERICH R, DONATH A, SPAHR A, ROSSI E. CONGENITAL LYSINE INTOLERANCE WITH PERIODIC AMMONIA INTOXICATION. Lancet. 1964 May 9;1(7341):1014–1015. [PubMed]
  • Hadorn B, Hanimann F, Anders P, Curtius HC, Halverson R. Free amino-acids in human sweat from different parts of the body. Nature. 1967 Jul 22;215(5099):416–417. [PubMed]
  • Herrin JT, McCredie DA. Peritoneal dialysis in the reduction of blood ammonia levels in a case of hyperammonaemia. Arch Dis Child. 1969 Apr;44(234):149–151. [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]
  • 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]
  • WESTALL RG. Argininosuccinic aciduria: identification and reactions of the abnormal metabolite in a newly described form of mental disease, with some preliminary metabolic studies. Biochem J. 1960 Oct;77:135–144. [PubMed]

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