Human Prion Disorders: Review of the Current Literature and a Twenty-Year Experience of the National Surveillance Center in the Czech Republic

Human prion disorders (transmissible spongiform encephalopathies, TSEs) are unique, progressive, and fatal neurodegenerative diseases caused by aggregation of misfolded prion protein in neuronal tissue. Due to the potential transmission, human TSEs are under active surveillance in a majority of coun...

Descripción completa

Detalles Bibliográficos
Autores principales: Jankovska, Nikol, Rusina, Robert, Bruzova, Magdalena, Parobkova, Eva, Olejar, Tomas, Matej, Radoslav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8534461/
https://www.ncbi.nlm.nih.gov/pubmed/34679519
http://dx.doi.org/10.3390/diagnostics11101821

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8534461/
https://www.ncbi.nlm.nih.gov/pubmed/34679519
http://dx.doi.org/10.3390/diagnostics11101821

Ejemplares similares