Distinct origins of dura mater graft-associated Creutzfeldt-Jakob disease: past and future problems

Dura mater graft-associated Creutzfeldt-Jakob disease (dCJD) can be divided into two subgroups that exhibit distinct clinical and neuropathological features, with the majority represented by a non-plaque-type of dCJD (np-dCJD) and the minority by a plaque-type of dCJD (p-dCJD). The two distinct phen...

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Detalles Bibliográficos
Autores principales: Kobayashi, Atsushi, Matsuura, Yuichi, Mohri, Shirou, Kitamoto, Tetsuyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3976164/
https://www.ncbi.nlm.nih.gov/pubmed/24685293
http://dx.doi.org/10.1186/2051-5960-2-32

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3976164/
https://www.ncbi.nlm.nih.gov/pubmed/24685293
http://dx.doi.org/10.1186/2051-5960-2-32

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