Hyperammonemic Encephalopathy in an Adolescent Patient of Citrullinemia Type 1 With an Atypical Presentation-Reference-Cited by-同舟云学术

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Hyperammonemic Encephalopathy in an Adolescent Patient of Citrullinemia Type 1 With an Atypical Presentation

Published:2021-05-19 Issue: Volume: Page:
ISSN:2168-8184
Container-title:Cureus
language:en
Short-container-title:

Author:

Ruxmohan Samir,Quinonez Jonathan,Choudhari Jinal,Poudel Sujan,Pandav Krunal

Publisher

Cureus, Inc.

Subject

Aerospace Engineering

Reference19 articles.

1. Urea cycle disorders. clinical features and diagnosis. (2021). Accessed: April 16, 2021: https://www.uptodate.com/contents/urea-cycle-disorders-clinical-features-and-diagnosis?search=Urea%20cycle%20disorder....

2. Citrullinemia Type I;Quinonez SC,2016

3. Hypomorphic citrullinaemia due to mutated ASS1 with episodic ataxia;Saini AG;BMJ Case Rep,2018

4. Citrullinemia type II. (2011). Accessed. April 26, 2021: https://rarediseases.info.nih.gov/diseases/10215/citrullinemia-type-ii.

5. Citrullinemias types 1 and 2. (1995). Accessed. April 26, 2021: https://www.medlink.com/article/citrullinemias_types_1_and_2.

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. Prenatal diagnosis of citrullinemia type 1; seven families with c.1168G>A mutation of Argininosuccinate synthetase 1 gene in Southwest Iran: A case series;International Journal of Reproductive BioMedicine (IJRM);2023-01-09

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