White matter hyperintensities in progranulin-associated frontotemporal dementia: A longitudinal GENFI study

Frontotemporal dementia (FTD) is a heterogeneous group of neurodegenerative disorders with both sporadic and genetic forms. Mutations in the progranulin gene (GRN) are a common cause of genetic FTD, causing either a behavioural presentation or, less commonly, language impairment. Presence on T2-weig...

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Detaylı Bibliyografya
Yayımlandı:Neuroimage Clin
Asıl Yazarlar: Sudre, Carole H., Bocchetta, Martina, Heller, Carolin, Convery, Rhian, Neason, Mollie, Moore, Katrina M., Cash, David M., Thomas, David L., Woollacott, Ione O.C., Foiani, Martha, Heslegrave, Amanda, Shafei, Rachelle, Greaves, Caroline, van Swieten, John, Moreno, Fermin, Sanchez-Valle, Raquel, Borroni, Barbara, Laforce, Robert, Masellis, Mario, Tartaglia, Maria Carmela, Graff, Caroline, Galimberti, Daniela, Rowe, James B., Finger, Elizabeth, Synofzik, Matthis, Vandenberghe, Rik, de Mendonça, Alexandre, Tagliavini, Fabrizio, Santana, Isabel, Ducharme, Simon, Butler, Chris, Gerhard, Alex, Levin, Johannes, Danek, Adrian, Frisoni, Giovanni B., Sorbi, Sandro, Otto, Markus, Zetterberg, Henrik, Ourselin, Sebastien, Cardoso, M. Jorge, Rohrer, Jonathan D.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Elsevier 2019
Konular:
Regular Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6911860/
https://ncbi.nlm.nih.gov/pubmed/31835286
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nicl.2019.102077
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