Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis

BACKGROUND: Frontotemporal dementia is a highly heritable neurodegenerative disorder. In about a third of patients, the disease is caused by autosomal dominant genetic mutations usually in one of three genes: progranulin (GRN), microtubule-associated protein tau (MAPT), or chromosome 9 open reading...

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Bibliografiset tiedot
Julkaisussa:Lancet Neurol
Päätekijät: Rohrer, Jonathan D, Nicholas, Jennifer M, Cash, David M, van Swieten, John, Dopper, Elise, Jiskoot, Lize, van Minkelen, Rick, Rombouts, Serge A, Jorge Cardoso, M, Clegg, Shona, Espak, Miklos, Mead, Simon, Thomas, David L, De Vita, Enrico, Masellis, Mario, Black, Sandra E, Freedman, Morris, Keren, Ron, MacIntosh, Bradley J, Rogaeva, Ekaterina, Tang-Wai, David, Carmela Tartaglia, Maria, Laforce, Robert, Tagliavini, Fabrizio, Tiraboschi, Pietro, Redaelli, Veronica, Prioni, Sara, Grisoli, Marina, Borroni, Barbara, Padovani, Alessandro, Galimberti, Daniela, Scarpini, Elio, Arighi, Andrea, Fumagalli, Giorgio, Rowe, James B, Coyle-Gilchrist, Ian, Graff, Caroline, Fallström, Marie, Jelic, Vesna, Ståhlbom, Anne Kinhult, Andersson, Christin, Thonberg, Håkan, Lilius, Lena, Frisoni, Giovanni B, Binetti, Giuliano, Pievani, Michela, Bocchetta, Martina, Benussi, Luisa, Ghidoni, Roberta, Finger, Elizabeth, Sorbi, Sandro, Nacmias, Benedetta, Lombardi, Gemma, Polito, Cristina, Warren, Jason D, Ourselin, Sebastien, Fox, Nick C, Rossor, Martin N
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2015
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6742501/
https://ncbi.nlm.nih.gov/pubmed/25662776
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/S1474-4422(14)70324-2
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