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 |
Number | Citing Articles |
1 |
Loredana Arhip, Javier Agreda, Clara Serrano-Moreno, Marta Motilla de la Cámara, María Luisa Carrascal Fabián, Atocha Bielza, Cristina Velasco Gimeno, Miguel Camblor, Irene Bretón, Cristina Cuerda. Two pregnancies of an ornithine carbamoyltransferase deficiency disease carrier and review of the literature. Nutrición Hospitalaria 2024; doi: 10.20960/nh.04867
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2 |
Yasuharu Ueno, Takuji Maeda, Satoshi Okamoto, Hideki Taniguchi. Hepatocytes. Methods in Molecular Biology 2022; 2544: 129 doi: 10.1007/978-1-0716-2557-6_9
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3 |
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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4 |
Ruoyi Ishikawa, Takamichi Sugimoto, Takafumi Abe, Narumi Ohno, Taku Tazuma, Mayumi Giga, Hiroyuki Naito, Tomoyuki Kono, Eiichi Nomura, Keiichi Hara, Tohru Yorifuji, Takemori Yamawaki. A 36-year-old Man with Repeated Short-term Transient Hyperammonemia and Impaired Consciousness with a Confirmed <i>Carbamoyl Phosphate Synthase 1</i> Gene Monoallelic Mutation. Internal Medicine 2022; 61(9): 1387 doi: 10.2169/internalmedicine.7961-21
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5 |
Yun-Xia Li, Xiao-Hong Gong, Mei-Chen Liu, Cheng Peng, Peng Li, Yi-Tao Wang. Investigation of Liver Injury of Polygonum multiflorum Thunb. in Rats by Metabolomics and Traditional Approaches. Frontiers in Pharmacology 2017; 8 doi: 10.3389/fphar.2017.00791
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6 |
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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7 |
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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8 |
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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9 |
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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