Sporadic Creutzfeldt-Jakob Disease and Other Proteinopathies in Comorbidity

Sporadic Creutzfeldt-Jakob Disease and Other Proteinopathies in Comorbidity

Background: Sporadic Creutzfeldt–Jakob disease (sCJD) is the most common type of a group of transmissible spongiform encephalopathies (prion diseases). The etiology of the sporadic form of CJD is still unclear. sCJD can occur in combination with other neurodegenerative diseases, which further compli...

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Bibliographic Details
Main Authors: Eva Parobkova, Julie van der Zee, Lubina Dillen, Christine Van Broeckhoven, Robert Rusina, Radoslav Matej
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-11-01
Series:Frontiers in Neurology
Subjects:
Creutzfeldt-Jakob disease
Alzheimer's disease
β amyloid
tau protein
neurodegenerative disease
Online Access:https://www.frontiersin.org/articles/10.3389/fneur.2020.596108/full

Internet

https://www.frontiersin.org/articles/10.3389/fneur.2020.596108/full

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