Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob disease

Sporadic Creutzfeldt-Jakob disease (sCJD) is a fatal and potentially transmissible neurodegenerative disease caused by misfolded prion proteins (PrP(Sc)). To date, effective therapeutics are not available and accurate diagnosis can be challenging. Clinical diagnostic criteria employ a combination of...

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Vydáno v:Lancet Neurol
Hlavní autoři: Hermann, Peter, Appleby, Brian, Brandel, Jean-Philippe, Caughey, Byron, Collins, Steven, Geschwind, Michael, Green, Alison, Haïk, Stephane, Kovacs, Gabor G, Ladogana, Anna, Llorens, Franc, Mead, Simon, Nishida, Noriyuki, Pal, Suvankar, Parchi, Piero, Pocchiari, Maurizio, Satoh, Katsuya, Zanusso, Gianluigi, Zerr, Inga
Médium: Artigo
Jazyk:Inglês
Vydáno: 2021
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Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC8285036/
https://ncbi.nlm.nih.gov/pubmed/33609480
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/S1474-4422(20)30477-4
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