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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...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
MDPI
2021
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| Materias: | |
| 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 |