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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Detalles Bibliográficos
Autores principales: Gushue, Danielle, Herbst, Allen, Sim, Valerie, McKenzie, Debbie, Aiken, Judd M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6277185/
https://www.ncbi.nlm.nih.gov/pubmed/30149773
http://dx.doi.org/10.1080/19336896.2018.1513317

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6277185/
https://www.ncbi.nlm.nih.gov/pubmed/30149773
http://dx.doi.org/10.1080/19336896.2018.1513317

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