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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Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Τόπος έκδοσης:Brain
Κύριοι συγγραφείς: 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
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: Oxford University Press 2019
Θέματα:
Original Articles
Διαθέσιμο Online: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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