Clonazepam is an effective treatment for hyperekplexia due to a SLC6A5 (GlyT2) mutation
Author:
Funder
Academical Medical Centre
Juliana Children's Hospital
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.22493/fullpdf
Reference7 articles.
1. Startle syndromes;Bakker;Lancet Neurol,2006
2. Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease;Rees;Nat Genet,2006
3. The anxiety disorders interview schedule for children;Silverman;Am Acad Child Adolesc Psychiatry,1988
4. A measure of anxiety symptoms among children;Spence;Behav Res Ther,1998
Cited by 14 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. Approach to exaggerated startle reflex: a case of hyperekplexia minor;BMJ Case Reports;2020-04
2. Novel mutations in SLC6A5 with benign course in hyperekplexia;Molecular Case Studies;2019-10-11
3. Hyperekplexia: Report on phenotype and genotype of 16 Jordanian patients;Brain and Development;2017-04
4. Synaptopathies: synaptic dysfunction in neurological disorders - A review from students to students;Journal of Neurochemistry;2016-09
5. Functional jerks, tics, and paroxysmal movement disorders;Handbook of Clinical Neurology;2016
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