선택 - 화살표키/엔터키 닫기 - ESC

 
"prion diseases"에 대한 세부 검색 결과입니다
MeSH(Medical Subject Headings) 맞춤 검색 (http://www.nlm.nih.gov) 결과 : 1 페이지: 1
  • Prion Diseases - 새창 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)
    Synonyms : Encephalopathies, Spongiform, Transmissible, Human Transmissible Spongiform Encephalopathies, Inherited, Inherited Human Transmissible Spongiform Encephalopathies, Prion Protein Diseases, Prion-Induced Disorder, Transmissible Spongiform Encephalopathies
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MeSH(Medical Subject Headings) 유사 검색 (http://www.nlm.nih.gov) 결과 : 0 페이지: 1
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