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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Detalhes bibliográficos
Publicado no:Neuroimage Clin
Main Authors: 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.
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2019
Assuntos:
Regular Article
Acesso em linha: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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