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...

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Hlavní autoři:	Nikol Jankovska, Robert Rusina, Magdalena Bruzova, Eva Parobkova, Tomas Olejar, Radoslav Matej
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	MDPI AG 2021-10-01
Edice:	Diagnostics
Témata:	transmissible spongiform encephalopathies prion protein Creutzfeldt–Jakob disease Gerstmann–Sträussler–Scheinker syndrome corneal donor
On-line přístup:	https://www.mdpi.com/2075-4418/11/10/1821
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