Genetic and phenotypic heterogeneity in sporadic and familial forms of paroxysmal dyskinesia-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Genetic and phenotypic heterogeneity in sporadic and familial forms of paroxysmal dyskinesia

Published:2012-06-30 Issue:1 Volume:260 Page:93-99
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Groffen Alexander J. A.,Klapwijk Thom,van Rootselaar Anne-Fleur,Groen Justus L.,Tijssen Marina A. J.

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,Neurology

Link

http://link.springer.com/content/pdf/10.1007/s00415-012-6592-5

Reference33 articles.

1. Bhatia KP (2001) Familial (idiopathic) paroxysmal dyskinesias: an update. Semin Neurol 21:69–74

2. Demirkiran M, Jankovic J (1995) Paroxysmal dyskinesias: clinical features and classification. Ann Neurol 38:571–579

3. Mink JW (2007) Paroxysmal dyskinesias. Curr Opin Pediatr 19:652–656

4. Bruno MK, Hallett M, Gwinn-Hardy K, Sorensen B, Considine E, Tucker S, Lynch DR, Mathews KD, Swoboda KJ, Harris J, Soong BW, Ashizawa T, Jankovic J, Renner D, Fu YH, Ptacek LJ (2004) Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteria. Neurology 63:2280–2287

5. Lee WL, Tay A, Ong HT, Goh LM, Monaco AP, Szepetowski P (1998) Association of infantile convulsions with paroxysmal dyskinesias (ICCA syndrome): confirmation of linkage to human chromosome 16p12-q12 in a Chinese family. Hum Genet 103:608–612

Cited by 46 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. Identification of a de novo CACNA1B variant and a start-loss ADRA2B variant in paroxysmal kinesigenic dyskinesia;Heliyon;2024-04

2. PhenoExam: gene set analyses through integration of different phenotype databases;BMC Bioinformatics;2022-12-31

3. PRRT2 Mutation and Serum Cytokines in Paroxysmal Kinesigenic Dyskinesia;Current Medical Science;2022-04

4. PhenoExam: an R package and Web application for the examination of phenotypes linked to genes and gene sets;2021-06-30

5. PRRT2 Related Epilepsies: A Gene Review;Journal of Pediatric Neurology;2021-05-21

同舟云学术

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