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Prion propagation estimated from brain diffusion MRI is subtype dependent in sporadic Creutzfeldt–Jakob disease

Sporadic Creutzfeldt–Jakob disease (sCJD) is a transmissible brain proteinopathy. Five main clinicopathological subtypes (sCJD-MM(V)1, -MM(V)2C, -MV2K, -VV1, and -VV2) are currently distinguished. Histopathological evidence suggests that the localisation of prion aggregates and spongiform lesions va...

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Detalles Bibliográficos
Publicado en:Acta Neuropathol
Main Authors: Pascuzzo, Riccardo, Oxtoby, Neil P., Young, Alexandra L., Blevins, Janis, Castelli, Gianmarco, Garbarino, Sara, Cohen, Mark L., Schonberger, Lawrence B., Gambetti, Pierluigi, Appleby, Brian S., Alexander, Daniel C., Bizzi, Alberto
Formato: Artigo
Idioma:Inglês
Publicado: Springer Berlin Heidelberg 2020
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC7360647/
https://ncbi.nlm.nih.gov/pubmed/32535770
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00401-020-02168-0
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