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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Bibliographic Details
Published in:Prion
Main Authors: Gushue, Danielle, Herbst, Allen, Sim, Valerie, McKenzie, Debbie, Aiken, Judd M.
Format: Artigo
Language:Inglês
Published: Taylor & Francis 2018
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Research Paper
Online Access: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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