Sporadic occurrence of fatal thalamic insomnia without a prion protein gene mutation.

被引：0
|
作者：
Nixon, R [1 ]
Mastrianni, J [1 ]
Roberts, J [1 ]
Prusiner, S [1 ]
DeArmond, S [1 ]
机构：
[1] UNIV CALIF SAN FRANCISCO,SAN FRANCISCO,CA 94143
来源：
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY | 1996年 / 55卷 / 05期
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：225 / 225
页数：1
相关论文
共 50 条
  • [1] Fatal sporadic insomnia (FSI): Fatal familial insomnia (FFI) phenotype without a mutation of the prion protein (PrP) gene
    Mastrianni, JA
    Nixon, R
    Layzer, R
    DeArmond, SJ
    Prusiner, SB
    [J]. NEUROLOGY, 1997, 48 (03) : 5036 - 5036
  • [2] Prion protein conformation in a patient with sporadic fatal insomnia
    Mastrianni, JA
    Nixon, R
    Layzer, R
    Telling, GC
    Han, D
    DeArmond, SJ
    Prusiner, SB
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (21): : 1630 - 1638
  • [3] FATAL FAMILIAL INSOMNIA, A PRION DISEASE WITH A MUTATION AT CODON-178 OF THE PRION PROTEIN GENE
    MEDORI, R
    TRITSCHLER, HJ
    LEBLANC, A
    VILLARE, F
    MANETTO, V
    CHEN, HY
    XUE, R
    LEAL, S
    MONTAGNA, P
    CORTELLI, P
    TINUPER, P
    AVONI, P
    MOCHI, M
    BARUZZI, A
    HAUW, JJ
    OTT, J
    LUGARESI, E
    AUTILIOGAMBETTI, L
    GAMBETTI, P
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1992, 326 (07): : 444 - 449
  • [4] FATAL FAMILIAL INSOMNIA (FFI) - A PRION DISEASE WITH A MUTATION AT CODON-178 OF THE PRION PROTEIN GENE
    GAMBETTI, P
    MEDORI, R
    TRITSCHLER, H
    LEBLANC, A
    MONTAGNA, P
    CORTELLI, P
    TINUPER, P
    MONARI, L
    TABATON, M
    PETERSEN, R
    AUTILIOGAMBETTI, L
    LUGARESI, E
    [J]. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1992, 51 (03): : 353 - 353
  • [5] Sporadic fatal familial insomnia or thalamic dementia
    Moonis, M
    Smith, TW
    Mullins, T
    Capellari, S
    Petersen, R
    Gambetti, P
    [J]. NEUROLOGY, 1996, 46 (02) : 5089 - 5089
  • [6] Thalamic form of Creutzfeldt-Jakob disease or fatal insomnia? Report of a sporadic case with normal prion protein genotype
    Koichi Kawasaki
    Koichi Wakabayashi
    Akio Kawakami
    Masami Higuchi
    Tetsuyuki Kitamoto
    Shoji Tsuji
    H. Takahashi
    [J]. Acta Neuropathologica, 1997, 93 : 317 - 322
  • [7] Thalamic form of Creutzfeldt-Jakob disease or fatal insomnia? Report of a sporadic case with normal prion protein genotype
    Kawasaki, K
    Wakabayashi, K
    Kawakami, A
    Higuchi, M
    Kitamoto, T
    Tsuji, S
    Takahashi, H
    [J]. ACTA NEUROPATHOLOGICA, 1997, 93 (03) : 317 - 322
  • [8] Articles reviewed: 1. A subtype of sporadic prion disease mimicking fatal familial insomnia. 2. Prion protein conformation in a patient with sporadic fatal insomnia
    Allen, Richard P.
    [J]. SLEEP MEDICINE, 2000, 1 (01) : 69 - 70
  • [9] Fatal familial insomnia with a mutation at codon 178 of the prion protein gene: First report from Japan
    Nagayama, M
    Shinohara, Y
    Furukawa, H
    Kitamoto, T
    [J]. NEUROLOGY, 1996, 47 (05) : 1313 - 1316
  • [10] Fatal sporadic insomnia (thalamic form of sporadic Creutzfeldt-Jakob disease).
    Parchi, P
    Capellari, S
    Chin, S
    Powers, JM
    Schwarz, HB
    Burns, DK
    Gambetti, P
    [J]. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1998, 57 (05): : 518 - 518
12345