Genetic screening and diagnosis in epilepsy?
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Neurology (clinical),Neurology
Reference50 articles.
1. Epi4K Consortium; Epilepsy PhenomeGenome Project. De novo mutations in epileptic encephalopathies.;Allen;Nature,2013
2. Antiepileptic drugs for the treatment of severe myoclonic epilepsy in infancy.;Brigo;Cochrane Database Syst Rev,2013
3. De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome.;Suls;Am J Hum Genet,2013
4. De novo mutations in HCN1 cause early infantile epileptic encephalopathy.;Nava;Nat Genet,2014
5. GABRA1 and STXBP1: novel genetic causes of Dravet syndrome.;Carvill;Neurology,2014
Cited by 9 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. Whole Exome Sequencing in South Africa: Stakeholder Views on Return of Individual Research Results and Incidental Findings;Frontiers in Genetics;2022-06-08
2. Experience in the management of patients with genetic epilepsies and epileptic encephalopathies in the outpatient practice;Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova;2021
3. Diagnostic Testing in Epilepsy Genetics Clinical Practice;Seizures;2018-05-02
4. Diagnostic exome sequencing of syndromic epilepsy patients in clinical practice;Clinical Genetics;2018-03-23
5. Recent advances in epilepsy genetics;Neuroscience Letters;2018-02
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