Variant Creutzfeldt-Jakob disease

被引：0
|
作者：
Will, RG [1 ]
机构：
[1] Western Gen Hosp, Natl CJD Surveillance Unit, Edinburgh EH4 2XU, Midlothian, Scotland
来源：
ACTA NEUROBIOLOGIAE EXPERIMENTALIS | 2002年 / 62卷 / 03期
关键词：
variant Creutzfeldt-Jakob disease; clinical features; investigations; epidemiology;
D O I：
暂无
中图分类号：
Q189 [神经科学];
学科分类号：
071006 ;
摘要：
Variant Creutzfeldt-Jakob disease is caused by the transmission of bovine spongiform encephalopathy to humans. The clinical and investigative features of variant OD are relatively distinct from sporadic CJD. The number of cases of vCJD are increasing with time in the UK, but the total future number of cases of vCJD is uncertain.
引用
收藏
页码：167 / 173
页数：7
相关论文
共 50 条
  • [41] Assessing the risk of transfusion-transmitted variant Creutzfeldt-Jakob disease: a European perspective
    Domanovic, Dragoslav
    Lewin, Antoine
    O'Leary, Peter
    Janner-Jametti, Tiziana
    El Dusouqui, Soraya Amar
    Sousa, Ana Paula
    Zaaije, Hans
    Roberts, Barnaby
    Bougard, Daisy
    Prati, Daniele
    Nordberg, Jonas
    Erikstrup, Christian
    Janssen, Mart
    Lieshout-Krikke, Ryanne
    Gubbe, Knut
    O'Flaherty, Niamh
    Mathy, Genevieve
    Chantillon, Andree-Marie
    Lehtisalo, Riikka
    Sorensen, Ofsteng H.
    Tiberghien, Pierre
    Thomas, Stephen
    BLOOD TRANSFUSION, 2024, 22 (05)
  • [42] Unusual Dopaminergic Depletion in Variant Creutzfeldt-Jakob Disease with Early and Rapid Cognitive Decline
    Magnin, Eloi
    Chopard, Gilles
    Galmiche, Jean
    Brandel, Jean-Philippe
    Rumbach, Lucien
    EUROPEAN NEUROLOGY, 2011, 65 (06) : 368 - 368
  • [43] Transmissible spongiform encephalopathies: Creutzfeldt-Jakob disease
    Rabenau, HF
    Preiser, W
    Doerr, HW
    CHIRURG, 1998, 69 (05): : 511 - 521
  • [44] Dealing with the uncertain risk of variant Creutzfeldt-Jakob disease transmission by coagulation replacement products
    Millar, Carolyn M.
    Makris, Mike
    BRITISH JOURNAL OF HAEMATOLOGY, 2012, 158 (04) : 442 - 452
  • [45] Both murine host and inoculum modulate expression of experimental variant Creutzfeldt-Jakob disease
    Bett, Cyrus
    Piccardo, Pedro
    Cervenak, Juraj
    Torres, Juan-Maria
    Asher, David M.
    Gregori, Luisa
    JOURNAL OF GENERAL VIROLOGY, 2018, 99 (03): : 422 - 433
  • [46] Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfeldt-Jakob disease
    Bishop, Matthew T.
    Diack, Abigail B.
    Ritchie, Diane L.
    Ironside, James W.
    Will, Robert G.
    Manson, Jean C.
    BRAIN, 2013, 136 : 1139 - 1145
  • [47] Bovine spongiform encephalopathy in cattle and the new variant form of Creutzfeldt-Jakob disease in humans.
    Groschup, MH
    DEUTSCHE TIERARZTLICHE WOCHENSCHRIFT, 1999, 106 (08): : 329 - 331
  • [48] Variant Creutzfeldt-Jakob disease strain is identical in individuals of two PRNP codon 129 genotypes
    Diack, Abigail B.
    Boyle, Aileen
    Plinston, Christopher
    Hunt, Emma
    Bishop, Matthew T.
    Will, Robert G.
    Manson, Jean C.
    BRAIN, 2019, 142 : 1416 - 1428
  • [49] Recent findings in the epidemiology of Creutzfeldt-Jakob disease in Hungary
    Majtenyi, C
    TRANSMISSIBLE SUBACUTE SPONGIFORM ENCEPHALOPATHIES: PRION DISEASES, 1996, : 399 - 403
  • [50] Epidemiology of Creutzfeldt-Jakob disease - Past and present uncertainties
    Alperovitch, A
    EUROPEAN JOURNAL OF NEUROLOGY, 1996, 3 (06) : 500 - 506
12345