Histotype-Dependent Oligodendroglial PrP Pathology in Sporadic CJD: A Frequent Feature of the M2C “Strain”

In sporadic Creutzfeldt-Jakob disease, molecular subtypes are neuropathologically well identified by the lesioning profile and the immunohistochemical PrP(d) deposition pattern in the grey matter (histotypes). While astrocytic PrP pathology has been reported in variant CJD and some less frequent his...

Descripción completa

Detalles Bibliográficos
Autores principales: Gelpi, Ellen, Klotz, Sigrid, Vidal-Robau, Nuria, Ricken, Gerda, Regelsberger, Günther, Ströbel, Thomas, Kalev, Ognian, Leoni, Marlene, Budka, Herbert, Kovacs, Gabor G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8473396/
https://www.ncbi.nlm.nih.gov/pubmed/34578377
http://dx.doi.org/10.3390/v13091796

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8473396/
https://www.ncbi.nlm.nih.gov/pubmed/34578377
http://dx.doi.org/10.3390/v13091796

Ejemplares similares