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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Detalhes bibliográficos
Publicado no:Brain
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2019
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6439322/
https://ncbi.nlm.nih.gov/pubmed/30847466
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awz039
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