Hyperammonemia caused by impaired mitochondrial ornithine transport in a patient with partial quantitative deficiency of ornithine carbamoyltransferase-Reference-Cited by-同舟云学术

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Hyperammonemia caused by impaired mitochondrial ornithine transport in a patient with partial quantitative deficiency of ornithine carbamoyltransferase

Published:1990-04 Issue:2 Volume:23 Page:143-147
ISSN:0009-9120
Container-title:Clinical Biochemistry
language:en
Short-container-title:Clinical Biochemistry

Author:

Kuno Tateo,Miyazaki Sumio,Inoue Ituro,Saheki Takeyori

Publisher

Elsevier BV

Subject

Clinical Biochemistry,General Medicine

Reference15 articles.

1. Hereditary disorders of the urea cycle in man: Biochemical and molecular approaches;Saheki;Rev Physiol Biochem Pharmacol,1987

2. Ornithine transcarbamylase deficiency: a cause of lethal neonatal hyperammonemia in males;Campbell;N Engl J Med,1973

3. Altered enzyme activities and citrulline synthesis in liver mitochondria from ornithine carbamoyltransferase-deficient sparsefur (ash) mice;Cohen;Biochem J,1989

4. The simulation of the urea cycle: Correlation of effects due to inborn errors in the catalytic properties of the enzymes with clinical-biochemical observations;Kuchel;Aust J Exp Biol Med Sci,1977

5. Role of argininosuccinate synthetase in the regulation of urea synthesis in the rat and argininosuccinate synthetase-associated metabolic disorder in man;Saheki;Adv Enzyme Regul,1980

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Novel aspects of glutamine synthetase in ammonia homeostasis;Neurochemistry International;2020-11

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