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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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Podrobná bibliografie
Vydáno v:Prion
Hlavní autoři: Saito, Natsumi, Ishihara, Tomohiko, Kasuga, Kensaku, Nishida, Mana, Ishiguro, Takanobu, Nozaki, Hiroaki, Shimohata, Takayoshi, Onodera, Osamu, Nishizawa, Masatoyo
Médium: Artigo
Jazyk:Inglês
Vydáno: Taylor & Francis 2018
Témata:
On-line přístup: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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