From Prion Diseases to Prion-Like Propagation Mechanisms of Neurodegenerative Diseases

Prion diseases are fatal neurodegenerative sporadic, inherited, or acquired disorders. In humans, Creutzfeldt-Jakob disease is the most studied prion disease. In animals, the most frequent prion diseases are scrapie in sheep and goat, bovine spongiform encephalopathy in cattle, and the emerging chro...

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Detalles Bibliográficos
Autores principales: Acquatella-Tran Van Ba, Isabelle, Imberdis, Thibaut, Perrier, Véronique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810426/
https://www.ncbi.nlm.nih.gov/pubmed/24222767
http://dx.doi.org/10.1155/2013/975832

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810426/
https://www.ncbi.nlm.nih.gov/pubmed/24222767
http://dx.doi.org/10.1155/2013/975832

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