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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Veröffentlicht in:Brain
Hauptverfasser: 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
Format: Artigo
Sprache:Inglês
Veröffentlicht: Oxford University Press 2019
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Original Articles
Online Zugang: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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