Number of the records: 1
prionózy
Record number d017096 Date 06.06.2025 Type M Topical term prionózy Other term English (Pseudonym) Dementias, Transmissible
English (Pseudonym) Spongiform Encephalopathies, Transmissible
English (Pseudonym) Transmissible Dementias
Slovak (Pseudonym) choroby priónové
Slovak (Pseudonym) encefalopatie spongiformné prenosné
Slovak (Pseudonym) encefalopatie spongioformné prenosné
Slovak (Pseudonym) encefalopatie špongioformné prenosné
Slovak (Pseudonym) demencie prenosné
See also (Later heading) scrapie
(Later heading) infekcie pomalé vírusové
UDC C01.207.800C10.228.228.800C10.574.843 Note A 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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Number of the records: 1