Hyperammonemia in a Woman with Late-onset Ornithine Transcarbamylase Deficiency-Reference-Cited by-同舟云学术

Hyperammonemia in a Woman with Late-onset Ornithine Transcarbamylase Deficiency

Published:2019-04-01 Issue:7 Volume:58 Page:937-942
ISSN:0918-2918
Container-title:Internal Medicine
language:en
Short-container-title:Intern. Med.

Author:

Koya Yudai¹,Shibata Michihiko¹,Senju Michio¹,Honma Yuichi¹,Hiura Masaaki¹,Ishii Masahiro²,Matsumoto Shirou³,Harada Masaru¹

Affiliation:

1. Third Department of Internal Medicine, School of Medicine, University of Occupational and Environmental Health, Japan

2. Department of Pediatrics, School of Medicine, University of Occupational and Environmental Health, Japan

3. Department of Pediatrics, Graduate School of Medical Sciences, Kumamoto University, Japan

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine,Internal Medicine

Link

https://www.jstage.jst.go.jp/article/internalmedicine/58/7/58_1851-18/_pdf

Reference26 articles.

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2. 2. Walker V. Severe hyperammonemia in adults not explained by liver disease. Ann Clin Biochem 49: 1-15, 2012.

3. 3. Treem WR. Inherited and acquired syndromes of hyperammonemia and encephalopathy in children. Semin Liver Dis 14: 236-258, 1994.

4. 4. De Jonghe B, Janier V, Abderrahim N, Hillion D, Lacherade JC, Outin H. Urinary tract infection and coma. Lancet 360: 996, 2002.

5. 5. Lora-Tamayo J, Palom X, Sarrá J, et al. Multiple myeloma and hyperammonemic encephalopathy: review of 27 cases. Clin Lymphoma Myeloma 8: 363-369, 2008.

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