Congenital Hyperammonemic Syndromes-Reference-Cited by-同舟云学术

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Congenital Hyperammonemic Syndromes

Published:1976-03 Issue:1 Volume:3 Page:3-14
ISSN:0095-5108
Container-title:Clinics in Perinatology
language:en
Short-container-title:Clinics in Perinatology

Author:

Shih Vivian E.

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology,Pediatrics, Perinatology, and Child Health

Reference46 articles.

1. Treatment of carbamyl phosphate synthetase deficiency with keto-analogues of essential amino acids;Batshaw;New Engl. J. Med,1975

2. Hereditary hyperammonaemia;Bruton;Brain,1970

3. Ornithine transcarbamylase deficiency;Campbell;A cause of lethal neonatal hyperammonemia in males. New Engl. J. Med,1973

4. X-linked transmission of structural ?ene mutations responsible for ornithine-transcarbamylase deficiencies;Cathelineau;Lancet,1973

5. Heterogenous mutations of the struc tural gene of human ornithine carbamyltransferase as observed in five personal cases;Cathelineau;Enzyme,1974

Cited by 21 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. Quo vadis ureagenesis disorders? A journey from 90 years ago into the future;Journal of Inherited Metabolic Disease;2024-06-04

2. Portosystemic Shunts;Small Animal Soft Tissue Surgery;2023-03-10

3. Urea cycle disorders;Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease;2020

4. Targeting CPS1 in the treatment of Carbamoyl phosphate synthetase 1 (CPS1) deficiency, a urea cycle disorder;Expert Opinion on Therapeutic Targets;2017-02-20

5. Portosystemic Shunts;Small Animal Soft Tissue Surgery;2014-07-18

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