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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...
Autores principales: | Jankovska, Nikol, Rusina, Robert, Bruzova, Magdalena, Parobkova, Eva, Olejar, Tomas, Matej, Radoslav |
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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/PMC8534461/ https://www.ncbi.nlm.nih.gov/pubmed/34679519 http://dx.doi.org/10.3390/diagnostics11101821 |
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