Epilepsy surgery as a treatment option for select patients with PCDH19-related epilepsy
Author:
Publisher
Elsevier BV
Subject
Behavioral Neuroscience,Neurology (clinical),Neurology
Reference23 articles.
1. Euro E-RESC, Epilepsy Phenome/Genome P EK. De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies. D Am J Hum Genet. 2014;95:360-370.
2. Effectiveness of antiepileptic therapy in patients with PCDH19 mutations;Lotte;Seizure,2016
3. Sporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects females;Depienne;PLoS Genet,2009
4. Mutations and deletions in PCDH19 account for various familial or isolated epilepsies in females;Depienne;Hum Mutat,2011
5. Defining the electroclinical phenotype and outcome of PCDH19-related epilepsy: A multicenter study;Trivisano;Epilepsia,2018
Cited by 4 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. Do germline genetic variants influence surgical outcomes in drug-resistant epilepsy?;Epilepsy Research;2024-10
2. Surgical outcomes of patients with genetically refractory epilepsy: A systematic review and meta-analysis;Seizure: European Journal of Epilepsy;2024-08
3. Epilepsy with PCDH19 mutation: polypharmacy as a consequence of the complexity and diversity of pathogenesis mechanisms;S.S. Korsakov Journal of Neurology and Psychiatry;2024
4. Evaluating Clinical Presentation and Long-Term Outcomes in Individuals with Genetic and Non-Genetic Epilepsy Treated with Epilepsy Surgery: A Single-Center Study;2023-12-04
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