Gerstmann-Sträussler-Scheinker disease: A case report
Author:
Publisher
Baishideng Publishing Group Inc.
Subject
General Medicine
Reference21 articles.
1. Pro→Leu change at position 102 of prinon protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome
2. Sporadic and familial CJD: classification and characterisation
3. Genetic prion disease: the EUROCJD experience
4. Gerstmann–Sträussler–Scheinker syndrome,fatal familial insomnia, and kuru: a review ofthese less common human transmissiblespongiform encephalopathies
5. Gerstmann-Straussler-Scheinker disease with mutation at codon 102 and methionine at codon 129 of PRNP in previously unreported patients
Cited by 6 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. Genetic forms of tauopathies: inherited causes and implications of Alzheimer’s disease-like TAU pathology in primary and secondary tauopathies;Journal of Neurology;2024-03-30
2. Case report: A Chinese patient with spinocerebellar ataxia finally confirmed as Gerstmann-Sträussler-Scheinker syndrome with P102L mutation;Frontiers in Neurology;2023-08-03
3. Miscellaneous CNS Viral Infections: Underappreciated Causes of Neurologic Disease;Viral and Fungal Infections of the Central Nervous System: A Microbiological Perspective;2023
4. Gerstmann—Sträussler disease: a familial case with common PRNP mutation and atypical features;Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova;2023
5. Gerstmann-Sträussler-Scheinker Disease: A Case Report;Journal of the Korean Society of Radiology;2023
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