Organic acid metabolism in a patient with ornithine transcarbamylase deficiency

Author:

Hiroko Kodama,Osamu Nose,Shintaro Okada,Ichiro Maki,Hitoshi Tajiri,Tetsuya Sano,Hyakuji Yabuuchi

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference18 articles.

1. Blood pyruvic-acid and α-keto-glutaric acid levels in liver disease and hepatic coma;Dawson;Lancet,1975

2. Acid-base and metabolic disturbances in fulminant hepatic failure;Record;Gut,1975

3. Plasma α-ketoglutarate in urea cycle enzymopathies and its role as a harbinger of hyperammonemic coma;Batshaw;Pediatr Res,1980

4. Hereditary orotic aciduria. II. A urinary screening test;Rogers;Pediatrics,1968

5. Adaptive characteristics of urea cycle enzymes in the rat;Schimke;J Biol Chem,1962

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