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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Sparad:
Bibliografiska uppgifter
I publikationen:Front Neurol
Huvudupphovsmän: Parobkova, Eva, van der Zee, Julie, Dillen, Lubina, Van Broeckhoven, Christine, Rusina, Robert, Matej, Radoslav
Materialtyp: Artigo
Språk:Inglês
Publicerad: Frontiers Media S.A. 2020
Ämnen:
Neurology
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC7735378/
https://ncbi.nlm.nih.gov/pubmed/33329348
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2020.596108
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