Novel Morphological Glial Alterations in the Spectrum of Prion Disease Types: A Focus on Common Findings

Human prion diseases are a group of rare fatal neurodegenerative diseases with sporadic, genetic, and acquired forms. They are neuropathologically characterized by pathological prion protein accumulation, neuronal death, and vacuolation. Classical immunological response has long been known not to pl...

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Detalles Bibliográficos
Autores principales: Garcés, Moisés, Guijarro, Isabel M., Ritchie, Diane L., Badiola, Juan J., Monzón, Marta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153175/
https://www.ncbi.nlm.nih.gov/pubmed/34068251
http://dx.doi.org/10.3390/pathogens10050596

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153175/
https://www.ncbi.nlm.nih.gov/pubmed/34068251
http://dx.doi.org/10.3390/pathogens10050596

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