1Mabbott NA, MacPherson GG. Prions and their lethal journey to t he brain[J]. Nat Rev Mierobiol,2006,4 ( 3 ) :201-211.
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 PrPsc type 2 in Japan [ J ]. J Neurol Neurosurg Psychiatry, 2004,75:485.
3Pereira E. Diffusion. weighted sequence on MRI for the diagnosis of Creutzfeldt-Jakob disease [ J ]. Arq Neurepsiquiatr, 2002,60:906-908.
4Shiga Y, Miyazawa K, Sato S, et al. Diffusion weighted MRIAbnormalities as an early diagnostic marker for Creutzfeldt-Jakob disease [J]. Neurology ,2004,63:443-449.
2Parchi P,Giese A,Capellari S,et al. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Am Neurol,1999,46:224-233.
3Rao CV,Brennan TG,Garcia JH. Computed tomography in the diagnosis of Creutzfeldt-Jakob disease. J Comput Assist Tomogr,1977,211-215.
4Kawai M,Twata M,Takatsu M,et al. When does the brain atrophy in Creutzfeldt-Jakob disease? Rinsho Shinkeigaku,1981,21:691-697.
5Galves S,Cartier L. Computed tomography findings in 15 cases of Creutzfeldt-Jakob disease with histological verification. J Neurol Neurosurg Psychiatry,1984,47:1244-1246.
6Berciano J,Diez C,Polo JM,et al. CT appearance of panencephalopathic and ataxic type of Creutzfeldt-Jakob disease. J Comput Assist Tomogr,1991,15:332-334.