1Ladogana A, Puopolo M, Croes EA, et al. Mortality from Creu -tzfeldt-Jakob disease and related disorders in Europe, Australia ,and Canada[J]. Neurology, 2005,64(9):1 586-1 591.
3Weissman C. Molecular genetics of transmissible spongiform en-cephalopathies[J]. J Biol Chem,1999,274(1):3--6.
4Prusiner SB. Prions[J]. Proc Natl Acad Sci USA, 1998, 95 (23):13 363-13 383
5Nakajima M, Yamada T, Kusuhara T, et al. Results of quinac -rine administration to patients with Creutzfeldt-Jakob disease[J]. Dement Geriatr Cogn Disord,2004,17(3):158-163.
2Fukushima R,Shiga Y,Nakamura M,et al. MRI characteristics of sporadic CJD with valine homozygosity at codon 129 of the prion protein gene and prp type 2 in Japan[J]. J Neurol Neurosurg Psychiatry,2004,75: 485.
3Cambier DM,Kantarci K,Werrell GA,et al.Lateralized and focal clinical,EEG,and FLAIR MRI abnormalities in Creutzfeldt-Jakob disease[J]. Clinical Neurophysiol,2003,114:1724.
4Lossu G,Melis M,Molari A,et al. Creutzfeldt-Jakob disease and literature review[J]. Neuro Sci,2003,24:138.
5Hill AF,Collinge J. Subclinical prion infection[J]. Trends Microbiol,2003,11:578.
6Amin SZ,Smith L,Luthert PJ,et al. minising the rist of prion transmission by contact tonometry[J]. Br Ophthalomol,2003,87:1360.?A
7van Evebroeck B,Quoilin S,Boons J,et al,A prospective study of CSF makers in 250 patients with possible Creutzfeldt-Jakob disease[J]. J Neurol Neurosurg Psychiatry,2003,74:1210.
8Narang HK. A clinical review of atypical cerebellum-type CJD and relationship to new varient CJD and bovine spongiform encetholopathy[J]. Exp Biol Med,2001,225:629.
9Kapure N,Ironside J,Abott P.Aneuropsychological-neuropathological case study of varient Creutzfeldt-Jakob disease[J]. Neurocase,2001,7:261.
10Collie DA,Summer DH,Sellar RJ,et al.Diagnosing varient Creutzfeldt-Jakob disease with pulvinar sign:MR imaging findings in 86 neuropathologically confirmed cases[J]. Am J Neuroradiol,2003,24:1561.
