Cargando…
White matter lesions in FTLD: distinct phenotypes characterize GRN and C9ORF72 mutations
Autores principales: | Ameur, Fatima, Colliot, Olivier, Caroppo, Paola, Ströer, Sebastian, Dormont, Didier, Brice, Alexis, Azuar, Carole, Dubois, Bruno, Le Ber, Isabelle, Bertrand, Anne |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4817905/ https://www.ncbi.nlm.nih.gov/pubmed/27066584 http://dx.doi.org/10.1212/NXG.0000000000000047 |
Ejemplares similares
-
Plasma NfL levels and longitudinal change rates in C9orf72 and GRN-associated diseases: from tailored references to clinical applications
por: Saracino, Dario, et al.
Publicado: (2021) -
White-matter abnormalities in presymptomatic GRN and C9orf72 mutation carriers
por: Lee, Hyunwoo, et al.
Publicado: (2022) -
Distinguishing post‐translational modifications in dominantly inherited frontotemporal dementias: FTLD‐TDP Type A (GRN) vs Type B (C9orf72)
por: Cracco, Laura, et al.
Publicado: (2022) -
Glia in FTLD-GRN: from supporting cast to leading role
por: Pinarbasi, Emile S., et al.
Publicado: (2023) -
Lateral Temporal Lobe: An Early Imaging Marker of the Presymptomatic GRN Disease?
por: Caroppo, Paola, et al.
Publicado: (2015)