The phenotypic expression of different mutations in transmissible familial Creutzfeldt-Jakob disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Epidemiology
Link
http://link.springer.com/content/pdf/10.1007/BF00143124.pdf
Reference24 articles.
1. BrownP., CathalaF., CastaigneP. and GajdusekD. (1986): Creutzfeldt-Jakob disease: clinical analysis of a consecutive series of 230 neuropathologically verified cases. - Ann. Neurol. 20: 597–602.
2. BrownP., GoldfarbL.G., BrownW.T., GoldgaberD., RubensteinR., KascsakR.J., GuiroyD. C., PiccardoP., BoellaardJ.W. and GajdusekD.C. (1991): Clinical and molecular genetic study of a large German kindred with Gerstmann-Strůssler-Scheinker syndrome. - Neurology 41: 375–379.
3. BrownP., GoldfarbL.G., CathalaF., VrbovskáA., SulimaM., NietoA., GibbsC.J. Jr and GajdusekD. C. (1991): The molecular genetics of familial Creutzfeldt-Jakob disease in France. - J. Neurol. Sci 105: 240–246.
4. Brown P.. Goldfarb L.G., McCombie W.R., Nieto A., Trapp S., Squillacote D.. Sheremata W.. Godec M.S., Gibbs C.J. Jr and Gajdusek D.C. (1992): Atypical Creutzfeldt-Jakob disease in an American family with an insert mutation in the PRNP amyloid precursor gene. - Neurology, in press.
5. CollingeJ., HardingA.E., OwenF., PoulterM., LofthouseR., BougheyA.M., ShahT. and CrowT.J. (1989): Diagnosis of Gerstmann-Straussler syndrome in familial dementia with prion protein gene analysis.- Lancet ii: 15–17.
Cited by 54 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. Analysis of non-human primate models for evaluating prion disease therapeutic efficacy;PLOS Pathogens;2022-08-22
2. Epilepsy in neurodegenerative diseases;Epileptic Disorders;2022-04
3. Prion Diseases;Viral Infections of Humans;2022
4. Phenotypic diversity of genetic Creutzfeldt–Jakob disease: a histo-molecular-based classification;Acta Neuropathologica;2021-07-29
5. Early sensory disturbances and seizures are common manifestations of familial Creutzfeldt-Jakob disease due to E200K PRNP mutation: Case report from two Peruvian families;Clinical Neurology and Neurosurgery;2021-03
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