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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Human Genome Epidemiology Literature Finder|Home|PHGKB
Human Genome Epidemiology Literature Finder
Last data update: Apr 25, 2024
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Seizures and UGT2B7[original query]
Early post-traumatic seizures are associated with valproic acid plasma concentrations and UGT1A6/CYP2C9 genetic polymorphisms in patients with severe traumatic brain injury.
Scandinavian journal of trauma, resuscitation and emergency medicine 2017 Aug 25 (1): 85.
Sun Yirui, Yu Jian, Yuan Qiang, Wu Xing, Wu Xuehai, Hu J
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Effects of UGT2B7, SCN1A and CYP3A4 on the therapeutic response of sodium valproate treatment in children with generalized seizures.
Seizure 2018 Apr 58 96-100.
Feng Weixing, Mei Shenghui, Zhu Leting, Yu Yazhen, Yang Weili, Gao Baoqin, Wu Xiaojuan, Zhao Zhigang, Fang Fa
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Effects of Comedication and Genetic Factors on the Population Pharmacokinetics of Lamotrigine: A Prospective Analysis in Chinese Patients With Epilepsy.
Frontiers in pharmacology 2019 8 10 832.
Wang Zhan-Zhang, Zhang Yue-Feng, Huang Wen-Can, Wang Xi-Pei, Ni Xiao-Jiao, Lu Hao-Yang, Hu Jin-Qing, Deng Shu-Hua, Zhu Xiu-Qing, Xie Huan-Shan, Chen Hong-Zhen, Zhang Ming, Qiu Chang, Wen Yu-Guan, Shang De-W
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Genetic polymorphisms of microsomal epoxide hydrolase and UDP-glucuronosyltransferase (UGT) and its effects on plasma carbamazepine levels and metabolic ratio in persons with epilepsy of South India: A cross-sectional genetic association study.
Indian journal of pharmacology 2023 8 55 (3): 149-154.
Shravan Venkatraman, Kesavan Ramasamy, Pradeep Pankajakshan Na
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Influence of EPHX1 c.337 T>C and UGT2B7*2 genetic polymorphisms on the requirement of carbamazepine maintenance dose in person with epilepsy (PWE) of Southern part of India: a cross-sectional genetic association study.
Drug metabolism and personalized therapy 2023 2 .
Venkatraman Shravan, Ramasamy Kesavan, Nair Pradeep P, Rajendran Priyadharsi
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 22, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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