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Prion Diseases

"Prion Diseases" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information
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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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This graph shows the total number of publications written about "Prion Diseases" by people in Harvard Catalyst Profiles by year, and whether "Prion Diseases" was a major or minor topic of these publication.
Bar chart showing 56 publications over 21 distinct years, with a maximum of 7 publications in 2020
To see the data from this visualization as text, click here.
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