Anomia is present pre-symptomatically in frontotemporal dementia due to MAPT mutations

INTRODUCTION: A third of frontotemporal dementia (FTD) is caused by an autosomal-dominant genetic mutation in one of three genes: microtubule-associated protein tau (MAPT), chromosome 9 open reading frame 72 (C9orf72) and progranulin (GRN). Prior studies of prodromal FTD have identified impaired exe...

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Detalles Bibliográficos
Autores principales: Bouzigues, Arabella, Russell, Lucy L., Peakman, Georgia, Bocchetta, Martina, Greaves, Caroline V., Convery, Rhian S., Todd, Emily, Rowe, James B., Borroni, Barbara, Galimberti, Daniela, Tiraboschi, Pietro, Masellis, Mario, Tartaglia, Maria Carmela, Finger, Elizabeth, van Swieten, John C., Seelaar, Harro, Jiskoot, Lize, Sorbi, Sandro, Butler, Chris R., Graff, Caroline, Gerhard, Alexander, Langheinrich, Tobias, Laforce, Robert, Sanchez-Valle, Raquel, de Mendonça, Alexandre, Moreno, Fermin, Synofzik, Matthis, Vandenberghe, Rik, Ducharme, Simon, Le Ber, Isabelle, Levin, Johannes, Danek, Adrian, Otto, Markus, Pasquier, Florence, Santana, Isabel, Rohrer, Jonathan D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Original Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9294015/
https://www.ncbi.nlm.nih.gov/pubmed/35348856
http://dx.doi.org/10.1007/s00415-022-11068-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9294015/
https://www.ncbi.nlm.nih.gov/pubmed/35348856
http://dx.doi.org/10.1007/s00415-022-11068-0

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