The insomnia phenotype in genetic Creutzfeldt–Jakob disease based on the E200K mutation

The aim of the presented study was to reveal the frequency of insomnia spells in E200K genetic Creutzfeldt–Jakob disease (gCJD) patients. Clinical records of 22 subjects diagnosed with E200K gCJD were retrospectively reviewed. The patients w/wo insomnia (n = 4, 18%/n = 18, 82%) did not differ in age...

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Detalles Bibliográficos
Autores principales: Feketeova, Eva, Jarcuskova, Dominika, Janakova, Alzbeta, Vitkova, Marianna, Dragasek, Jozef, Gdovinova, Zuzana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Short Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000144/
https://www.ncbi.nlm.nih.gov/pubmed/30922182
http://dx.doi.org/10.1080/19336896.2019.1590938

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000144/
https://www.ncbi.nlm.nih.gov/pubmed/30922182
http://dx.doi.org/10.1080/19336896.2019.1590938

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