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中国克-雅病流行病学及临床特征文献分析 被引量:2

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摘要 克罗伊茨费尔特一雅各布病(Creutzfeldt-Jakob disease,CJD),国内学者简称克-雅病即皮质纹状体-脊髓变性,是一个罕见的疾患,在世界范围内的发病率大约是每年百万分之一,本病国外报道较多,国内首次报道为1980年[1]。
出处 《中华传染病杂志》 CAS CSCD 北大核心 2014年第3期190-192,共3页 Chinese Journal of Infectious Diseases
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参考文献15

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二级参考文献35

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共引文献14

同被引文献20

  • 1徐全刚,吴卫平,黄德晖,张家堂,郎森阳,蒲传强.MR扩散加权成像对Creutzfeldt-Jakob病的诊断意义[J].中华放射学杂志,2005,39(6):624-626. 被引量:12
  • 2叶静,刘峥,朴月善,卢德宏,李存江,贾建平,徐庚,谌燕飞,董秀敏.遗传性朊蛋白病一家系的临床、病理和基因突变分析[J].中华神经科杂志,2007,40(11):732-735. 被引量:3
  • 3Gao C, Shi Q, Tian C, et al. The Epidemiological, clinical, and laboratory features of sporadic Creutzfeldt-Jakob disease patients in China: surveillance data from 2006 to 2010[J]. PLoS One,2011,6(8):e24231.
  • 4Zhao W, Zhang JT, Xing XW, et al. Chinese specific characteristics of sporadic Creutzfeldt-Jakob disease: a retrospective analysis of 57 cases[J]. PLoS One,2013,8(3):e58442.
  • 5Kim MO, Geschwind MD. Clinical update of Jakob-Creutzfeldt disease [ J ]. Curt Opin Neurol, 2015,28 : 302-310.
  • 6Zerr I, Kallenberg K, Summers DM, et al. Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease [ J ]. Brain, 2009, 132 : 2659-2668.
  • 7Shiga Y, Miyazawa K, Sato S, et al. Diffusion-weighted MRIabnormalities as an early diagnostic marker for Creutzfeldt-Jakob disease I J ]. Neurology, 2004, 63 (3) : 443-449.
  • 8Vitali P, Maeeagnano E, Caverzasi E, et al. Diffilsion-weighted MIll hyperintensity patterns differentiate CJD from other rapid dementias [ J ]. Neurology, 2011,76(20) : 1711-1719.
  • 9Brandel JP, Delasnerie-Laupretre N, Laplanche JL, et al. Diagnosis of Creutzfeldt-Jakob disease : effect of clinical criteria on incidence estimates I J ]. Neurolo~~, 2000, 54 (5) : 1095-1099.
  • 10Appel S, Chapman J, Cohen OS, et al. Seizures in E200K familial and sporadic Creutzfeldt-Jakob disease [ J 1. Acta Neurol Seand, 2015, 131 (3) : 152-157.

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