Imaging and CSF analyses effectively distinguish CJD from its mimics

OBJECTIVE: To review clinical and investigation findings in patients referred to a specialist prion clinic who were suspected to have sporadic Creutzfeldt-Jakob disease (sCJD) and yet were found to have an alternative final diagnosis. METHODS: Review the clinical findings and investigations in 214 p...

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Detalles Bibliográficos
Autores principales: Rudge, Peter, Hyare, Harpreet, Green, Alison, Collinge, John, Mead, Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2018
Materias:
Neurodegeneration
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5909756/
https://www.ncbi.nlm.nih.gov/pubmed/29142140
http://dx.doi.org/10.1136/jnnp-2017-316853

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5909756/
https://www.ncbi.nlm.nih.gov/pubmed/29142140
http://dx.doi.org/10.1136/jnnp-2017-316853

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