Two Siblings with Complete Carbamyl Phosphate Synthetase I Deficiency-Reference-Cited by-同舟云学术

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Two Siblings with Complete Carbamyl Phosphate Synthetase I Deficiency

Published:1984-03 Issue:1 Volume:26 Page:16-19
ISSN:1328-8067
Container-title:Pediatrics International
language:en
Short-container-title:Pediatr Int

Author:

Kakinuma Hiroaki,Ohtake Akira,Ogura Namiko,Takayanagi Masaki,Nakajima Hironori,Nishioka Tadashi,Matsuura Yoko,Takeuchi Yutaka,Asanuma Katsumi

Publisher

Wiley

Subject

Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1442-200X.1984.tb02182.x/fullpdf

Reference12 articles.

1. Treatment of Inborn Errors of Urea Synthesis

2. Lethal Neonatal Deficiency of Carbamyl Phosphate Synthetase

3. Increased excretion of N-carbamoyl compounds in patients with urea cycle defects

4. Massive pulmonary hemorrhage as a presenting feature in congenital hyperammonemia

Cited by 5 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. Amino Acids;Volpe's Neurology of the Newborn;2018

2. Hyperammonemia and Other Disorders of Amino Acid Metabolism;Neurology of the Newborn;2008

3. Hereditary disorders of the urea cycle in man: Biochemical and molecular approaches;Reviews of Physiology, Biochemistry and Pharmacology;1987

4. A Carbamyl Phosphate Synthetase I Deficiency with No Detectable Messenger RNA Activity;Pediatrics International;1984-06

5. A female case of ornithine transcarbamylase deficiency with marked computed tomographic abnormalities of the brain;Brain and Development;1984-01

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