Cerebral perfusion changes in presymptomatic genetic frontotemporal dementia: a GENFI study

Genetic forms of frontotemporal dementia are most commonly due to mutations in three genes, C9orf72, GRN or MAPT, with presymptomatic carriers from families representing those at risk. While cerebral blood flow shows differences between frontotemporal dementia and other forms of dementia, there is l...

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Detalles Bibliográficos
Autores principales: Mutsaerts, Henri J M M, Mirza, Saira S, Petr, Jan, Thomas, David L, Cash, David M, Bocchetta, Martina, de Vita, Enrico, Metcalfe, Arron W S, Shirzadi, Zahra, Robertson, Andrew D, Tartaglia, Maria Carmela, Mitchell, Sara B, Black, Sandra E, Freedman, Morris, Tang-Wai, David, Keren, Ron, Rogaeva, Ekaterina, van Swieten, John, Laforce, Robert, Tagliavini, Fabrizio, Borroni, Barbara, Galimberti, Daniela, Rowe, James B, Graff, Caroline, Frisoni, Giovanni B, Finger, Elizabeth, Sorbi, Sandro, de Mendonça, Alexandre, Rohrer, Jonathan D, MacIntosh, Bradley J, Masellis, Mario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6439322/
https://www.ncbi.nlm.nih.gov/pubmed/30847466
http://dx.doi.org/10.1093/brain/awz039

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6439322/
https://www.ncbi.nlm.nih.gov/pubmed/30847466
http://dx.doi.org/10.1093/brain/awz039

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