Sporadic Creutzfeldt-Jakob disease with MM1-type prion protein and plaques - Reply

被引:0
|
作者
Ishida, C
Kitamoto, T
Yamada, M
机构
关键词
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
引用
收藏
页码:1239 / 1239
页数:1
相关论文
共 50 条
  • [21] An autopsy case of MM1-type sporadic Creutzfeldt-Jakob disease with 1-month total disease duration presenting with early disease pathology
    Iwasaki, Yasushi
    Kato, Hiroko
    Mimuro, Maya
    Ando, Tetsuo
    Yoshida, Mari
    PRION, 2016, 10 : S84 - S84
  • [22] Plaque-type deposition of prion protein in the damaged white matter of sporadic Creutzfeldt-Jakob disease MM1 patients
    Kobayashi, Atsushi
    Arima, Kunimasa
    Ogawa, Masafumi
    Murata, Miho
    Fukuda, Takahiro
    Kitamoto, Tetsuyuki
    ACTA NEUROPATHOLOGICA, 2008, 116 (05) : 561 - 566
  • [23] Plaque-type deposition of prion protein in the damaged white matter of sporadic Creutzfeldt-Jakob disease MM1 patients
    Atsushi Kobayashi
    Kunimasa Arima
    Masafumi Ogawa
    Miho Murata
    Takahiro Fukuda
    Tetsuyuki Kitamoto
    Acta Neuropathologica, 2008, 116 : 561 - 566
  • [24] Type of prion protein in UK farmers with Creutzfeldt-Jakob disease
    Hill, AF
    Will, RG
    Ironside, J
    Collinge, J
    LANCET, 1997, 350 (9072): : 188 - 188
  • [25] Spatial pattern of prion protein deposits in patients with sporadic Creutzfeldt-Jakob disease
    Armstrong, RA
    Cairns, NJ
    Lantos, PL
    NEUROPATHOLOGY, 2001, 21 (01) : 19 - 24
  • [26] Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease
    Zanusso, G
    Ferrari, S
    Cardone, F
    Zampieri, P
    Gelati, M
    Fiorini, M
    Farinazzo, A
    Gardiman, M
    Cavallaro, T
    Bentivoglio, M
    Righetti, PG
    Pocchiari, M
    Rizzuto, N
    Monaco, S
    NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (08): : 711 - 719
  • [27] Prion protein glycotype analysis in familial and sporadic Creutzfeldt-Jakob disease patients
    Cardone, F
    Liu, QG
    Petraroli, R
    Ladogana, A
    D'Alessandro, M
    Arpino, C
    Di Bari, M
    Macchi, G
    Pocchiari, M
    BRAIN RESEARCH BULLETIN, 1999, 49 (06) : 429 - 433
  • [28] Prion protein genotype and pathological phenotype studies in sporadic Creutzfeldt-Jakob disease
    MacDonald, ST
    Sutherland, K
    Ironside, JW
    NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 1996, 22 (04) : 285 - 292
  • [29] Prion protein accumulation in eyes of patients with sporadic and variant Creutzfeldt-Jakob disease
    Head, MW
    Northcott, V
    Rennison, K
    Ritchie, D
    McCardle, L
    Bunn, TJR
    McLennan, NF
    Ironside, JW
    Tullo, AB
    Bonshek, RE
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2003, 44 (01) : 342 - 346
  • [30] Comparison of the clinical course of Japanese MM1-type sporadic Creutzfeldt-Jakob disease between subacute spongiform encephalopathy and panencephalopathic-type
    Iwasaki, Yasushi
    Tatsumi, Shinsui
    Mimuro, Maya
    Kitamoto, Tetsuyuki
    Yoshida, Mari
    CLINICAL NEUROLOGY AND NEUROSURGERY, 2014, 121 : 59 - 63