MeSH 搜索器

Prion Diseases

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)
推出的年份: 1993
副标题
树号: C01.207.800, C10.228.228.800, C10.574.843
MeSH 单一 ID: D017096
进入的组:
  • Dementias, Transmissible
  • Dementia, Transmissible
  • Transmissible Dementia
  • Transmissible Dementias
  • Encephalopathies, Spongiform, Transmissible
  • Prion-Induced Disorders
  • Prion-Induced Disorder
  • Disorder, Prion-Induced
  • Disorders, Prion-Induced
  • Prion Induced Disorder
  • Transmissible Spongiform Encephalopathies
  • Prion Disease
  • Prion-Associated Disorders
  • Spongiform Encephalopathies, Transmissible
  • Encephalopathies, Transmissible Spongiform
  • Encephalopathy, Transmissible Spongiform
  • Spongiform Encephalopathy, Transmissible
  • Transmissible Spongiform Encephalopathy
  • Prion Protein Diseases
  • Prion Protein Disease
  • Human Transmissible Spongiform Encephalopathies, Inherited
  • Inherited Human Transmissible Spongiform Encephalopathies
早前的内容:
  • Slow Virus Diseases (1966-1992)

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