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

Author:

Levin B.,Abraham J. M.,Oberholzer V. G.,Burgess E. A.

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference20 articles.

1. A disease, probably hereditary, characterized by severe mental deficiency and a constant gross abnormality of aminoacid metabolism;Allan, J.D.; Cusworth, D.C.; Dent, C.E.; Wilson, V.K.;Lancet,1958

2. Comparative biochemistry of urea synthesis. I. Methods for the quantitative assay of urea cycle enzymes in liver;Brown, Jr., G.W.; Cohen, P.P.;J. biol. Chem,1959

3. L-lysine dehydrogenase deficiency in a patient with congenital lysine intolerance;Burgi, W.; Richterich, R.; Colombo, J.P.;Nature (Lond.),1966

4. Congenital lysine intolerance with periodic ammonia intoxication: a defect in L-lysine degradation;Colombo, J.P.; Burgi, W.; Richterich, R.; Rossi, E.;Metabolism,1967

5. The estimation of plasma ammonia by ion exchange;Fenton, J.C.B.;Clin. chim. Acta,1962

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