Cerebral cortex swelling in V180I genetic Creutzfeldt–Jakob disease: comparative imaging study between sporadic and V180I genetic Creutzfeldt–Jakob disease in the early stage

The most common genetic Creutzfeldt-Jakob disease (gCJD) in Japan is caused by a point mutation in which isoleucine replaces valine at codon 180 of the prion protein (PrP) gene (V180I gCJD). Evidence suggests that cerebral cortex swelling, which appears as abnormal hyperintensities on diffusion-weig...

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Detalles Bibliográficos
Autores principales: Muroga, Yuki, Sugiyama, Atsuhiko, Mukai, Hiroki, Hashiba, Jun, Yokota, Hajime, Satoh, Katsuya, Kitamoto, Tetsuyuki, Wang, Jiaqi, Ito, Shoichi, Kuwabara, Satoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10075330/
https://www.ncbi.nlm.nih.gov/pubmed/37013454
http://dx.doi.org/10.1080/19336896.2023.2197809

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10075330/
https://www.ncbi.nlm.nih.gov/pubmed/37013454
http://dx.doi.org/10.1080/19336896.2023.2197809

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