1Prince LA, Mann D, Reilly T. Creutzfeldt Jakob disease: an emergency department presentation of a rare disease [ J ]. J Emergency Medicine, 2006,31(1) :41-44.
2Onodera T, Sakudo A, Wu G, et al. Bovine spongiform encephalopathy in Japan:history and recent studies on oxidative stress in prion disease [ J]. Microbiol-Imunol, 2006,50 ( 8 ) : 565-578.
3Knight R. Creutzfeldt Jakob disease: a rare cause of dementia in elderly persons[J]. Clin Infect Disease,2006,43(3) :340-346.
4Cllins SJ, Sanehez JP, Masters CL, et al. Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt Jakob disease[J]. Brain,2006,129(Pt 9) :2 278-2 287.
5Shiga Y, Wakabayashi H, Miyazawa K, et al. 14-3-3 protein levels and isoform patterns in the eerebrospinal fluid of Creutzfeldt Jakob disease patiens in the progressive and terminal stages[J]. J Clin Neurosci, 2006, 13 (6) : 661.665.
6Zerr I, Bodemer M, Gefller O, et al. Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt Jakob disease [J] .Ann Neurol, 1998,43 ( 1 ) : 32-40.
