• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[Creutzfeldt-Jakob disease in France. Value of familial forms. Is there a gene controlling the length of the incubation period?].

作者信息

Cathala F, Brown P, Chatelain J, Castaigne P, Gajdusek C

出版信息

Presse Med. 1986 Feb 22;15(8):379-82.

PMID:2938156
Abstract

An extensive search for patients who died of Creutzfeld-Jakob disease in France between 1968 and 1982 resulted in the discovery of 327 cases, 233 of which were histologically proven and 29 transmitted to animals; 17 patients belonged to 6 families. Further investigations among members of these 6 families yielded 21 additional cases, i.e. a total of 38 familial cases. Studies among sibships suggested an autosomal dominant pattern of transmission but did not exclude lateral contamination infancy. The patients' age at death was 10 to 15 years lower than that of the total of French cases and seemed to be a characteristic of each individual family. This suggests that, as in scrapie, a gene may control the length of the incubation period.

摘要

相似文献

1
[Creutzfeldt-Jakob disease in France. Value of familial forms. Is there a gene controlling the length of the incubation period?].
Presse Med. 1986 Feb 22;15(8):379-82.
2
Familial Creutzfeldt-Jakob disease in France: epidemiological implications.法国的家族性克雅氏病:流行病学意义
Eur J Epidemiol. 1986 Dec;2(4):252-64. doi: 10.1007/BF00419489.
3
Familial Creutzfeldt-Jakob disease in Chile.智利的家族性克雅氏病
J Neurol Sci. 1983 Apr;59(1):139-47. doi: 10.1016/0022-510x(83)90087-4.
4
The familial occurrence of Creutzfeldt-Jakob disease and Alzheimer's disease.克雅氏病和阿尔茨海默病的家族性发病情况。
Brain. 1981 Sep;104(3):535-58. doi: 10.1093/brain/104.3.535.
5
Familial Creutzfeldt-Jakob disease. Autosomal dominance in 14 members over 3 generations.
J Neurol Sci. 1980 Sep;47(3):343-51. doi: 10.1016/0022-510x(80)90087-8.
6
Creutzfeldt-Jakob disease in France: III. Epidemiological study of 170 patients dying during the decade 1968--1977.法国的克雅氏病:III. 对1968年至1977年这十年间死亡的170例患者的流行病学研究
Ann Neurol. 1979 Nov;6(5):438-46. doi: 10.1002/ana.410060511.
7
The French surveillance network of Creutzfeldt-Jakob disease. Epidemiological data in France and worldwide.法国克雅氏病监测网络。法国及全球的流行病学数据。
Transfus Clin Biol. 2013 Sep;20(4):395-7. doi: 10.1016/j.tracli.2013.02.029. Epub 2013 Apr 12.
8
The epidemiology of Creutzfeldt-Jakob disease: conclusion of a 15-year investigation in France and review of the world literature.克雅氏病的流行病学:法国一项为期15年的调查结论及全球文献综述
Neurology. 1987 Jun;37(6):895-904. doi: 10.1212/wnl.37.6.895.
9
[Familial Creutzfeldt-Jakob disease. A clinical and pathological study of three cases in a family with eight affected members in three generations (author's transl)].[家族性克雅氏病。对一个三代中有八名患者的家族中的三例病例的临床和病理学研究(作者译)]
Rev Neurol (Paris). 1978 Mar;134(3):165-81.
10
Genetic control of scrapie and Creutzfeldt-Jakob disease in mice.小鼠中羊瘙痒病和克雅氏病的遗传控制。
J Immunol. 1983 Jul;131(1):491-6.

引用本文的文献

1
Prion protein gene analysis in three kindreds with fatal familial insomnia (FFI): codon 178 mutation and codon 129 polymorphism.三个致命性家族性失眠症(FFI)家系的朊蛋白基因分析:密码子178突变与密码子129多态性
Am J Hum Genet. 1993 Oct;53(4):822-7.
2
Creutzfeldt-Jakob disease in England and Wales, 1980-1984: a case-control study of potential risk factors.1980 - 1984年英格兰和威尔士的克雅氏病:潜在风险因素的病例对照研究
J Neurol Neurosurg Psychiatry. 1988 Sep;51(9):1113-9. doi: 10.1136/jnnp.51.9.1113.