Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Hyperammonemia and CPS1[original query] |
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4217C>A polymorphism in carbamoyl-phosphate synthase 1 gene may not associate with hyperammonemia development during valproic acid-based therapy. Epilepsy research 2014 Aug 108 (6): 1046-51. Inoue Kazuyuki, Suzuki Eri, Takahashi Toshiki, Yamamoto Yoshiaki, Yazawa Rei, Takahashi Yukitoshi, Imai Katsumi, Miyakawa Kou, Inoue Yushi, Tsuji Daiki, Hayashi Hideki, Itoh Kunihi |
Is there any relationship between mutation in CPS1 Gene and pregnancy loss? International journal of reproductive biomedicine 2019 8 17 (5): 371-4. Talebi Mehrdad, Yahya Vahidi Mehrjardi Mohammad, Kalhor Kambiz, Dehghani Mohammadre |
CPS1 T1405N polymorphism, HDL cholesterol, homocysteine and renal function are risk factors of VPA induced hyperammonemia among epilepsy patients. Epilepsy research 2019 May 154 139-143. Chen Lanlan, Tian Qiuxiang, Zhang Miaoran, Chen Deyu, Gao Xue, Yang Hongqun, Li Haitao, Li Chengnan, Wen Jianping, Li Yulin, Tian Xin, Chen Pe |
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