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)
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)
Prior analytics Aristotle Commentaries Early works to 1800 : David the Invincible, commentary on Aristotle's Prior analytics : critical Old Armenian text / with an English translation, introduction, and notes by Aram Topchyan ; [edited] by Aram Topchyan
Here are entered works on knowledge acquired either formally or non-formally before entrance into a specific program, usually in the area of post-secondary education
Prior, Peter, 1905- : Straight from the Yudaman's mouth : the life story of Peter Prior before, during and after the Robert Curry days, never told before / by Renarta Prior