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prionózy

  1. Subject h.prionózy
    Subject h.Prion Diseases
    Entry termschoroby priónové
    encefalopatie spongiformné prenosné
    encefalopatie spongioformné prenosné
    encefalopatie špongioformné prenosné
    demencie prenosné
    English X referencesDementias, Transmissible
    Spongiform Encephalopathies, Transmissible
    Transmissible Dementias
    Scope note in EnglishA group of genetic, infectious, or sporadic degenerative human and animal nervous system disorders associated with abnormal PRIONS. These diseases are characterized by conversion of the normal prion protein to an abnormal configuration via a post-translational process. In humans, these conditions generally feature DEMENTIA; ATAXIA; and a fatal outcome. Pathologic features include a spongiform encephalopathy without evidence of inflammation. The older literature occasionally refers to these as unconventional SLOW VIRUS DISEASES. (From Proc Natl Acad Sci USA 1998 Nov 10;95(23):13363-83)
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    (2) - MeSH descriptor
    (15) - CiBaMed
    (1) - ELECTRONIC RESOURCES
    (11) - BOOKS
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Number of the records: 1  

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