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Creutzfeldt-Jakob病诊断标准的探讨 被引量:8

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摘要 1996年3月20日英国海绵状脑病顾问委员会向世界公告:英国已发现10例变异型Creutzfeldt-Jakob病(CJD),立即引起全世界极大关注[1]。至2006年全世界已发现变异型CJD140例。因此,世界卫生组织要求有条件的国家立即行动起来,对CJD进行全球性监测。中国卫生部与国家疾病控制中心决定,自2003年起在全国范围内有计划、
作者 林世和
出处 《中华神经科杂志》 CAS CSCD 北大核心 2008年第4期223-225,共3页 Chinese Journal of Neurology
基金 国家自然科学基金资助项目(30470589)
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参考文献20

  • 1林世和.对Creutzfeldt-Jakob病的思考与展望[J].临床神经病学杂志,2005,18(1):1-3. 被引量:19
  • 2林世和,王为民,赵节绪,江新梅,宋晓南.颅脑眼手术后的Creutzfeldt-Jakob病[J].中国神经精神疾病杂志,2000,26(4):193-195. 被引量:4
  • 3Brandel JP, Delasnerie-Laupretre N, Laplanche JL, et al. Diagnosis of Creutzieldt-Jakob disease : effect of clinical criteria on incidence estimates. Neurology ,2000,54 : 1095-1099.
  • 4林世和,赵节绪,江新梅,宋晓南,王为民,徐惠芹,王跃山.我国Creutzfeldt-Jakob病的若干特殊性[J].中华神经科杂志,1998,31(6):330-332. 被引量:15
  • 5林世和,赵节绪,江新梅,宋晓南.70岁以上老年Creutzfeldt-Jakob病三例报告[J].中华神经科杂志,2003,36(5):399-400. 被引量:4
  • 6Lemstra AW, Schoenmaker N, Rozemuller-Kwakkel AJ, et al. The association of neuroleptic sensitivity in Lewy body diseases with a false positive clinical diagnosis of Creutzfeldt-Jakob disease, Int J Geriatr Psychiatry ,2006,21:1031-1035.
  • 7Sanchez-Valle R, Santamaria J, Rey MJ, et al. MM1 variant of sporadic Creutzfeldt-Jakob disease with long duration akinetic mutism state. Neurologia ,2006,21:444-446.
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  • 9Kawamoto Y, Akiguchi I, Jarius C, et al. Enhanced expression of 14-3-3 proteins in reactive in Creutzfeldt-Jakob disease brains. Acta Neuropathol,2004, 108:302-308.
  • 10林世和,赵节绪,于雪凡,张俊格,杨蕴天.Creutzfeldt-Jakob病脑组织14-3-3蛋白表达及其意义[J].中华神经科杂志,2007,40(5):295-297. 被引量:4

二级参考文献38

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共引文献45

同被引文献52

  • 1李硕,赵节绪.Creutzfeldt-Jakob病的诊断新进展[J].临床神经病学杂志,2004,17(4):309-310. 被引量:8
  • 2林世和.对Creutzfeldt-Jakob病的思考与展望[J].临床神经病学杂志,2005,18(1):1-3. 被引量:19
  • 3于雪凡,林世和,赵珩.脑脊液14-3-3蛋白对不同类型Creutzfeldt-Jakob病的诊断价值[J].临床神经病学杂志,2006,19(1):77-78. 被引量:15
  • 4林世和,于雪凡,孙瑞红,高金立.脑脊液神经蛋白质对临床拟诊Creutzfeldt—Jakob病的早期诊断价值[J].中华神经科杂志,2007,40(4):253-256. 被引量:9
  • 5Hort J, Valis M, Waberzinek G, et al. Proportion oftau protein to phosphorylated tau protein CSF levels in differential diagnosis of dementia. Nervenarzt, 2008, 79: 891-892, 894-896, 898.
  • 6Satoh K, Shirabe S, Tsujino A, et al. Total tan protein in cerebrospinal fluid and diffusion-weighted MRI as an early diagnostic marker for Creutzfeldt-Jakob disease. Dement Geriatr Cogn Disord, 2007, 24: 207-212.
  • 7Sanchez-Juan P, Sanchez-Valle R, Green A, et al. Influence of timing on CSF tests value for Creutzfeldt-Jakob disease diagnosis. J Neurol, 2007, 254: 901-906.
  • 8Castellani RJ, Colueci M, Xie Z, et al. Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt-Jakob disease. Neurology, 2004, 63: 436-442.
  • 9Hung CI, Wang PS, Soong BW, et al. Blind source separation of concurrent disease related patterns from EEG in Creutzfeldt-Jakob disease for assisting early diagnosis. Ann Biomed Eng, 2007, 35 : 2168-2179.
  • 10Eggenberger E. Prion disease. Neurol Clin, 2007, 25: 833-842.

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