Late-onset and Slow-progressing Lafora Disease in Four Siblings with EPM2B Mutation-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Late-onset and Slow-progressing Lafora Disease in Four Siblings with EPM2B Mutation

Published:2005-10 Issue:10 Volume:46 Page:1695-1697
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:Epilepsia

Author:

Baykan Betul,Striano Pasquale,Gianotti Stefania,Bebek Nerses,Gennaro Elena,Gurses Candan,Zara Federico

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2005.00272.x/fullpdf

Reference8 articles.

1. A novel protein tyrosine phosphatase gene is mutated in progressive myoclonus epilepsy of the Lafora type (EPM2)

2. Mutations in NHLRC1 cause progressive myoclonus epilepsy

3. Lafora disease due to EPM2B mutations: A clinical and genetic study

4. Antimyoclonic Effect of Levetiracetam in 13 Patients with Unverricht-Lundborg Disease: Clinical Observations

Cited by 64 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. Lafora disease: A rare case report;Indian Journal of Pathology and Oncology;2024-09-15

2. Lafora progressive myoclonus epilepsy: Disease mechanism and therapeutic attempts;Journal of Biosciences;2024-01-20

3. Developmental and Inherited Liver Disease;MacSween's Pathology of the Liver;2024

4. ILAE Genetics Literacy series: Progressive myoclonus epilepsies;Epileptic Disorders;2023-09-06

5. Prognostic value of pathogenic variants in Lafora Disease: systematic review and meta-analysis of patient-level data;Orphanet Journal of Rare Diseases;2023-09-02

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