A female carrier of ornithine carbamoyltransferase deficiency masquerading as attention deficit-hyperactivity disorder-Reference-Cited by-同舟云学术

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A female carrier of ornithine carbamoyltransferase deficiency masquerading as attention deficit-hyperactivity disorder

Published:2014-09 Issue:8 Volume:36 Page:734-737
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Kim Se Hee,Lee Jin Sook,Lim Byung Chan,Kim Ki Joong,Hwang Yong Seoung,Park June Dong,Cheon Jung-Eun,Kim In-One,Kim Boong-Nyun,Chae Jong-Hee

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health

Reference14 articles.

1. Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea-cycle enzymopathies;Msall;N Engl J Med,1984

2. Risk of serious illness in heterozygotes for ornithine transcarbamylase deficiency;Batshaw;J Pediatr,1986

3. Under recognition of late onset ornithine transcarbamylase deficiency;Schultz;Arch Dis Child,2000

4. Neuropsychiatric manifestations in late-onset urea cycle disorder patients;Serrano;J Child Neurol,2010

5. Late-onset ornithine transcarbamylase deficiency: a potentially fatal yet treatable cause of coma;Crosbie;Crit Care Resusc,2009

Cited by 9 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. Health-related quality of life in a systematically assessed cohort of children and adults with urea cycle disorders;Molecular Genetics and Metabolism;2023-11

2. Delayed recognition of autism spectrum disorder and attention-deficit/hyperactivity disorder in a girl with ornithine transcarbamylase deficiency: A case report;Medicine;2023-02-22

3. Physical, cognitive, and social status of patients with urea cycle disorders in Japan;Molecular Genetics and Metabolism Reports;2021-06

4. Gene delivery corrects N-acetylglutamate synthase deficiency and enables insights in the physiological impact of L-arginine activation of N-acetylglutamate synthase;Scientific Reports;2021-02-11

5. Multimodal imaging in urea cycle-related neurological disease – What can imaging after hyperammonemia teach us?;Translational Science of Rare Diseases;2020-08-03

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