Page 152 - Read Online
P. 152

Zhao et al.                                                                                                                                                             Developments in auxiliary examination of CJD

           65.  Young GS, Geschwind MD, Fischbein NJ, Martindale JL, Henry RG,   Criteria  for Creutzfeldt-Jakob  Disease (CJD), 2010.  Available
               Liu S, Lu Y, Wong S, Liu H, Miller BL, Dillon WP. Diffusion-weighted   from:  http://www.cdc.gov/prions/cjd/diagnostic-criteria.html.  [Last
               and fluid-attenuated inversion recovery imaging in Creutzfeldt-Jakob   accessed on June 21, 2017]
               disease:  high  sensitivity  and  specificity  for  diagnosis.  AJNR  Am  J   68.  Nagoshi K, Sadakane A, Nakamura Y, Yamada, Mizusawa H. Duration
               Neuroradiol 2005;26:1551-62.
           66.  Meissner B, Körtner K, Bartl M, Jastrow U, Mollenhauer B, Schröter   of prion disease is longer in Japan than in other countries. J Epidemiol
               A, Finkenstaedt  M,  Windl  O, Poser S, Kretzschmar  HA, Zerr  I.   2011;21:255-62.
               Sporadic Creutzfeldt-Jakob disease: magnetic resonance imaging and   69.  Atalay FÖ, Tolunay Ş, Özgün G, Bekar A, Zarifoğlu M. Creutzfeldt-
               clinical findings. Neurology 2004;63:450-6.       Jakob disease: report of four cases and review of the literature. Turk
           67.  Centers for Disease Control and Prevention.  CDC’s Diagnostic   Patoloji Derg 2015;31:148-52.







































































            144                                                                        Neuroimmunology and Neuroinflammation ¦ Volume 4 ¦ July 21, 2017
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