The genetic variant “C588T” of GABARG2 is linked to childhood idiopathic generalized epilepsy and resistance to antiepileptic drugs
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Neurology,General Medicine
Reference32 articles.
1. Epilepsy in children and adolescents;Whelees,2013
2. Sodium channel mutations in epilepsy and other neurological disorders;Meisler;J Clin Invest,2005
3. Mechanisms of genetic epilepsies;Hedrich;E-Neuroforum,2013
4. Mutation screening of the γ-aminobutyric acid type-A receptor subunit γ2 gene in Korean patients with childhood absence epilepsy;Kim;J Clin Neurol,2012
5. Association analysis of GABRG2 polymorphisms with febrile seizures;Chou;Pediatr Res,2003
Cited by 25 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Review of pharmacogenetics of antiseizure medications: focusing on genetic variants of mechanistic targets;Frontiers in Pharmacology;2024-08-20
2. Coexistence of temporal lobe epilepsy and idiopathic generalized epilepsy;Epilepsy & Behavior;2024-02
3. Association between the SLC6A11 rs2304725 and GABRG2 rs211037 polymorphisms and drug-resistant epilepsy: a meta-analysis;Frontiers in Physiology;2023-05-19
4. On Complexity and Emergence: Linking the Hypotheses of Pharmacoresistance in Epilepsy;Pharmacoresistance in Epilepsy;2023
5. GABRG2 C588T Polymorphism Is Associated with Idiopathic Generalized Epilepsy but Not with Antiepileptic Drug Resistance in Pakistani Cohort;BioMed Research International;2022-11-15
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3