Applicability of long-term electroencephalography in pre-mortem diagnosis of Creutzfeldt–Jakob disease: A case report

Creutzfeldt–Jakob disease accounts for more than 90% of all sporadic prion disease cases. The molecular MM2 genotype has been divided into cortical and thalamic subtypes based on structures involved and is characterized clinically by progressive dementia without ataxia or typical electroencephalogra...

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Detalles Bibliográficos
Autores principales: Attaripour Isfahani, Sanaz, Dougherty, Michelle, Gliebus, Gediminas Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5734438/
https://www.ncbi.nlm.nih.gov/pubmed/29276596
http://dx.doi.org/10.1177/2050313X17744482

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5734438/
https://www.ncbi.nlm.nih.gov/pubmed/29276596
http://dx.doi.org/10.1177/2050313X17744482

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