Clinical heterogeneity of frontotemporal dementia and Parkinsonism linked to chromosome 17 caused by MAPT N279K mutation in relation to tau positron emission tomography features

BACKGROUND: While mechanistic links between tau abnormalities and neurodegeneration have been proven in frontotemporal dementia and parkinsonism linked to chromosome 17 caused by MAPT mutations, variability of the tau pathogenesis and its relation to clinical progressions in the same MAPT mutation c...

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Detalles Bibliográficos
Autores principales: Ikeda, Aya, Shimada, Hitoshi, Nishioka, Kenya, Takanashi, Masashi, Hayashida, Arisa, Li, Yuanzhe, Yoshino, Hiroyo, Funayama, Manabu, Ueno, Yuji, Hatano, Taku, Sahara, Naruhiko, Suhara, Tetsuya, Higuchi, Makoto, Hattori, Nobutaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Brief Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6593784/
https://www.ncbi.nlm.nih.gov/pubmed/30773680
http://dx.doi.org/10.1002/mds.27623

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6593784/
https://www.ncbi.nlm.nih.gov/pubmed/30773680
http://dx.doi.org/10.1002/mds.27623

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