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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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| Argitaratua izan da: | Lancet Neurol |
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| Egile Nagusiak: | , , , , , , , , , , , , , , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2021
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| Gaiak: | |
| Sarrera elektronikoa: | 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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