At the intersection of toxicology, psychiatry, and genetics: a diagnosis of ornithine transcarbamylase deficiency-Reference-Cited by-同舟云学术

At the intersection of toxicology, psychiatry, and genetics: a diagnosis of ornithine transcarbamylase deficiency

Published:2013-09 Issue:9 Volume:31 Page:1420.e5-1420.e6
ISSN:0735-6757
Container-title:The American Journal of Emergency Medicine
language:en
Short-container-title:The American Journal of Emergency Medicine

Author:

Sloas Harold Andrew,Ence Thomas C.,Mendez Donna R.,Cruz Andrea T.

Publisher

Elsevier BV

Subject

Emergency Medicine,General Medicine

Reference11 articles.

1. Urea cycle enzymes;Brusilow,2001

2. Urea cycle disorders;Leonard;Semin Neonatol,2002

3. Roth KS, Steiner RD. “Ornithine Transcarbamylase Deficiency”. 2012. MS. Creighton University School of Medicine, Omaha. Ornithine Transcabamylase Deficiency. EMedicine, 2 Apr. 2012. Web

4. Ammonia toxicity and its prevention in inherited defects of the urea cycle;Walker;Diabetes Obes Metab,2009

5. “X-chromosome Inactivation”. - Glossary Entry. Genetics Home Reference, 2012. Web. 23 Apr. 2012.

Cited by 6 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. Patients with Genetic Syndromes;Massachusetts General Hospital Comprehensive Clinical Psychiatry;2025

2. Challenges in diagnosing and managing adult patients with urea cycle disorders;Journal of Inherited Metabolic Disease;2019-05-08

3. Inborn Errors of Metabolism with Hyperammonemia;Pediatric Clinics of North America;2018-04

4. Liver involvement in urea cycle disorders: a review of the literature;Journal of Inherited Metabolic Disease;2017-09-12

5. Psychiatric adult-onset of urea cycle disorders: A case-series;Molecular Genetics and Metabolism Reports;2017-09