• 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

Genetic Creutzfeldt-Jakob disease mimicking chronic inflammatory demyelinating polyneuropathy.

作者信息

Weckhuysen Dorien, Schrooten Maarten, Demaerel Philippe, Van Broeckhoven Christine, Tousseyn Thomas, Kovacs Gabor G, Van Damme Philip

机构信息

Departments of Neurology (D.W., M.S., P.V.D.), Radiology (P.D.), and Pathology (T.T.), University Hospitals Leuven; KU Leuven (M.S.), University of Leuven, Department of Neurosciences, Experimental Neurology, Laboratory for Cognitive Neurology, Leuven; Neurodegenerative Brain Diseases Group (C.V.B.), Department of Molecular Genetics, VIB, Antwerp; Laboratory of Neurogenetics (C.V.B.), Institute Born-Bunge, University of Antwerp, Belgium; Institute of Neurology (G.G.K.), Medical University of Vienna, Austria; KU Leuven (P.V.D.), University of Leuven, Department of Neurosciences, Experimental Neurology and Leuven Research Institute for Neuroscience and Disease, Leuven; and VIB (P.V.D.), Vesalius Research Center, Laboratory of Neurobiology, Leuven, Belgium.

出版信息

Neurol Neuroimmunol Neuroinflamm. 2015 Oct 29;2(6):e173. doi: 10.1212/NXI.0000000000000173. eCollection 2015 Dec.

DOI:10.1212/NXI.0000000000000173
PMID:26568971
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4630682/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f52/4630682/c3436f0c2637/NEURIMMINFL2015006775FF1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f52/4630682/c3436f0c2637/NEURIMMINFL2015006775FF1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f52/4630682/c3436f0c2637/NEURIMMINFL2015006775FF1.jpg

相似文献

1
Genetic Creutzfeldt-Jakob disease mimicking chronic inflammatory demyelinating polyneuropathy.酷似慢性炎症性脱髓鞘性多发性神经病的遗传性克雅氏病。
Neurol Neuroimmunol Neuroinflamm. 2015 Oct 29;2(6):e173. doi: 10.1212/NXI.0000000000000173. eCollection 2015 Dec.
2
Childhood chronic inflammatory demyelinating polyneuropathy: an overview of 10 cases in the modern era.儿童慢性炎症性脱髓鞘性多发性神经病:现代10例病例概述
J Child Neurol. 2014 Jan;29(1):43-8. doi: 10.1177/0883073812471719. Epub 2013 Jan 29.
3
White matter involvement in sporadic Creutzfeldt-Jakob disease.散发性克雅氏病的白质受累。
Brain. 2014 Dec;137(Pt 12):3339-54. doi: 10.1093/brain/awu298. Epub 2014 Nov 2.
4
[Human prion diseases: the Hungarian experience].[人类朊病毒病:匈牙利的经验]
Ideggyogy Sz. 2007 Nov 30;60(11-12):447-52.
5
Demyelinating peripheral neuropathy in Creutzfeldt-Jakob disease.克雅氏病中的脱髓鞘性周围神经病
Muscle Nerve. 1992 Nov;15(11):1234-9. doi: 10.1002/mus.880151103.
6
Prospective 10-year surveillance of human prion diseases in Japan.日本朊病毒病前瞻性 10 年监测。
Brain. 2010 Oct;133(10):3043-57. doi: 10.1093/brain/awq216. Epub 2010 Sep 20.
7
Sporadic Creutzfeldt-Jakob disease mimicking variant Creutzfeldt-Jakob disease.酷似变异型克雅氏病的散发性克雅氏病
Arch Neurol. 2003 May;60(5):767-70. doi: 10.1001/archneur.60.5.767.
8
Segmental somatosensory-evoked potentials as a diagnostic tool in chronic inflammatory demyelinating polyneuropathies, and other sensory neuropathies.节段性体感诱发电位作为慢性炎症性脱髓鞘性多发性神经病及其他感觉神经病的诊断工具。
Neurophysiol Clin. 2014 Sep;44(3):267-80. doi: 10.1016/j.neucli.2014.08.006. Epub 2014 Aug 23.
9
Chronic Inflammatory Demyelinating Polyneuropathy Manifesting as Neuropathy With Liability to Pressure Palsies: A Case Report.表现为易患压迫性麻痹的神经病变的慢性炎症性脱髓鞘性多发性神经病:一例报告
J Clin Neuromuscul Dis. 2015 Dec;17(2):78-83. doi: 10.1097/CND.0000000000000094.
10
Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: UK cases 1991-2002.散发性而非变异型克雅氏病中的朊病毒蛋白异质性:1991 - 2002年英国病例
Ann Neurol. 2004 Jun;55(6):851-9. doi: 10.1002/ana.20127.

引用本文的文献

1
Demyelinating neuropathy as the initial presentation of familial E200K Creutzfeldt-Jakob disease in two patients.脱髓鞘性神经病作为两例家族性E200K型克雅氏病的首发表现
Ann Clin Transl Neurol. 2025 Mar;12(3):653-658. doi: 10.1002/acn3.52296. Epub 2025 Jan 12.
2
Prion type 2 selection in sporadic Creutzfeldt-Jakob disease affecting peripheral ganglia.朊病毒 2 型在影响周围神经节的散发性克雅氏病中的选择。
Acta Neuropathol Commun. 2021 Nov 24;9(1):187. doi: 10.1186/s40478-021-01286-4.
3
Creutzfeldt-Jakob disease with unusual presentation of peripheral neuropathy and ophthalmoplegia.

本文引用的文献

1
Genetic Creutzfeldt-Jakob disease associated with the E200K mutation: characterization of a complex proteinopathy.与 E200K 突变相关的遗传 Creutzfeldt-Jakob 病:一种复杂的蛋白病特征。
Acta Neuropathol. 2011 Jan;121(1):39-57. doi: 10.1007/s00401-010-0713-y. Epub 2010 Jul 1.
2
Severe and rapidly evolving peripheral neuropathy revealing sporadic Creutzfeldt-Jakob disease.
J Neurol. 2009 Jan;256(1):134-6. doi: 10.1007/s00415-009-0037-9. Epub 2009 Feb 7.
3
Creutzfeldt-Jakob disease with amyotrophy and demyelinating polyneuropathy.伴有肌萎缩和脱髓鞘性多发性神经病的克雅氏病
具有周围神经病变和眼肌麻痹异常表现的克雅氏病
Avicenna J Med. 2018 Oct-Dec;8(4):153-156. doi: 10.4103/ajm.AJM_77_18.
Arch Neurol. 2002 Nov;59(11):1811-4. doi: 10.1001/archneur.59.11.1811.
4
Impairment of the peripheral nervous system in Creutzfeldt-Jakob disease.克雅氏病患者周围神经系统的损伤
Arch Neurol. 2002 Sep;59(9):1430-6. doi: 10.1001/archneur.59.9.1430.
5
Diffusion-weighted magnetic resonance imaging in Creutzfeldt-Jakob disease.
Lancet. 1997 Mar 22;349(9055):847-8. doi: 10.1016/s0140-6736(05)61750-3.
6
Peripheral neuropathy in Creutzfeldt-Jakob disease.
Neurology. 1997 Mar;48(3):784. doi: 10.1212/wnl.48.3.784.
7
Demyelinating peripheral neuropathy with Creutzfeldt-Jakob disease and mutation at codon 200 of the prion protein gene.
Neurology. 1996 Apr;46(4):1123-7. doi: 10.1212/wnl.46.4.1123.