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14-3-3 and enolase abundances in the CSF of Prion diseased rats
Creutzfeldt-Jakob disease (CJD) is characterized by an extended asymptomatic preclinical phase followed by rapid neurodegeneration. There are no effective treatments. CJD diagnosis is initially suspected based upon the clinical presentation of the disease and the exclusion of other etiologies. Neuro...
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| Pubblicato in: | Prion |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Taylor & Francis
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6277185/ https://ncbi.nlm.nih.gov/pubmed/30149773 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/19336896.2018.1513317 |
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