FATAL FAMILIAL INSOMNIA AND THE WIDENING SPECTRUM OF PRION DISEASES

被引:30
作者
GAMBETTI, P [1 ]
PETERSEN, R [1 ]
MONARI, L [1 ]
TABATON, M [1 ]
AUTILIOGAMBETTI, L [1 ]
CORTELLI, P [1 ]
MONTAGNA, P [1 ]
LUGARESI, E [1 ]
机构
[1] UNIV BOLOGNA,INST NEUROL,I-40126 BOLOGNA,ITALY
关键词
D O I
10.1093/oxfordjournals.bmb.a072657
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
[No abstract available]
引用
收藏
页码:980 / 994
页数:15
相关论文
共 58 条
  • [1] THE SEARCH FOR SCRAPIE AGENT NUCLEIC-ACID
    AIKEN, JM
    MARSH, RF
    [J]. MICROBIOLOGICAL REVIEWS, 1990, 54 (03) : 242 - 246
  • [2] ALPER T, 1987, P113
  • [3] BEESEN RA, 1992, J VIROL, V66, P2096
  • [4] FAMILIAL CREUTZFELDT-JAKOB DISEASE (CODON-200 MUTATION) WITH SUPRANUCLEAR PALSY
    BERTONI, JM
    BROWN, P
    GOLDFARB, LG
    RUBENSTEIN, R
    GAJDUSEK, DC
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1992, 268 (17): : 2413 - 2415
  • [5] SUPRANUCLEAR GAZE PALSY IN FAMILIAL CREUTZFELDT-JAKOB DISEASE
    BERTONI, JM
    LABEL, LS
    SACKELLERES, JC
    HICKS, SP
    [J]. ARCHIVES OF NEUROLOGY, 1983, 40 (10) : 618 - 622
  • [6] A PRP GENE CODON-178 BASE SUBSTITUTION AND A 24-BP INTERSTITIAL DELETION IN FAMILIAL CREUTZFELDT-JAKOB DISEASE
    BOSQUE, PJ
    VNENCAKJONES, CL
    JOHNSON, MD
    WHITLOCK, JA
    MCLEAN, MJ
    [J]. NEUROLOGY, 1992, 42 (10) : 1864 - 1870
  • [7] BOUDOURESQUES J, 1976, REV NEUROL-FRANCE, V132, P623
  • [8] PHENOTYPIC CHARACTERISTICS OF FAMILIAL CREUTZFELDT-JAKOB DISEASE ASSOCIATED WITH THE CODON-178ASN PRNP MUTATION
    BROWN, P
    GOLDFARB, LG
    KOVANEN, J
    HALTIA, M
    CATHALA, F
    SULIMA, M
    GIBBS, CJ
    GAJDUSEK, DC
    [J]. ANNALS OF NEUROLOGY, 1992, 31 (03) : 282 - 285
  • [9] BROWN P, 1992, REV NEUROL, V148, P317
  • [10] THE MOLECULAR-GENETICS OF FAMILIAL CREUTZFELDT-JAKOB DISEASE IN FRANCE
    BROWN, P
    GOLDFARB, LG
    CATHALA, F
    VRBOVSKA, A
    SULIMA, M
    NIETO, A
    GIBBS, CJ
    GAJDUSEK, DC
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1991, 105 (02) : 240 - 246