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Case Report: A patient with spinocerebellar ataxia type 31 and sporadic Creutzfeldt-Jakob disease

We report a Japanese patient with spinocerebellar ataxia type 31 (SCA31) and sporadic Creutzfeldt-Jakob disease (sCJD). A 52-year-old man developed progressive cognitive impairment after the appearance of cerebellar symptoms. Brain MR diffusion-weighted imaging (DWI) demonstrated a slowly expanding...

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Bibliografski detalji
Izdano u:Prion
Glavni autori: Saito, Natsumi, Ishihara, Tomohiko, Kasuga, Kensaku, Nishida, Mana, Ishiguro, Takanobu, Nozaki, Hiroaki, Shimohata, Takayoshi, Onodera, Osamu, Nishizawa, Masatoyo
Format: Artigo
Jezik:Inglês
Izdano: Taylor & Francis 2018
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6016509/
https://ncbi.nlm.nih.gov/pubmed/29411683
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/19336896.2018.1436926
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