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Feb 28, 2017 (publication date) through Dec 2, 2023
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Publication Name
World Journal of Hepatology
ISSN
1948-5182
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Kido J, Kawasaki T, Mitsubuchi H, Kamohara H, Ohba T, Matsumoto S, Endo F, Nakamura K. Hyperammonemia crisis following parturition in a female patient with ornithine transcarbamylase deficiency. World J Hepatol 2017; 9(6): 343-348 [PMID: 28293384 DOI: 10.4254/wjh.v9.i6.343] |
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| URL: | https://www.wjgnet.com/1948-5182/full/v9/i6/343.htm |
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| 2 |
Mehnoosh Torkzaban, Andrew Haddad, Jason K. Baxter, Vincenzo Berghella, William A. Gahl, Huda B. Al‐Kouatly. Maternal ornithine transcarbamylase deficiency, a genetic condition associated with high maternal and neonatal mortality every clinician should know: A systematic review. American Journal of Medical Genetics Part A 2019; 179(10): 2091 doi: 10.1002/ajmg.a.61329
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MariaAnna Messina, Federica Raudino, Riccardo Iacobacci, Concetta Meli, Agata Fiumara. New ratio as a useful marker for early diagnosis of proximal urea cycle disorders. Clinica Chimica Acta 2021; 520: 154 doi: 10.1016/j.cca.2021.06.011
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Dan Yu, Guoyan Lu, Rajah Mowshica, Yan Cheng, Fumin Zhao. Clinical and cranial MRI features of female patients with ornithine transcarbamylase deficiency. Medicine 2019; 98(33): e16827 doi: 10.1097/MD.0000000000016827
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Jun Kido, Shirou Matsumoto, Tetsuya Ito, Shinichi Hirose, Kaori Fukui, Kanako Kojima-Ishii, Yuichi Mushimoto, Shinobu Yoshida, Mika Ishige, Norio Sakai, Kimitoshi Nakamura. Physical, cognitive, and social status of patients with urea cycle disorders in Japan. Molecular Genetics and Metabolism Reports 2021; 27: 100724 doi: 10.1016/j.ymgmr.2021.100724
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Jun Kido, Shirou Matsumoto, Hiroshi Mitsubuchi, Fumio Endo, Kimitoshi Nakamura. Early liver transplantation in neonatal-onset and moderate urea cycle disorders may lead to normal neurodevelopment. Metabolic Brain Disease 2018; 33(5): 1517 doi: 10.1007/s11011-018-0259-6
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