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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Regular Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6911860/
https://www.ncbi.nlm.nih.gov/pubmed/31835286
http://dx.doi.org/10.1016/j.nicl.2019.102077

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6911860/
https://www.ncbi.nlm.nih.gov/pubmed/31835286
http://dx.doi.org/10.1016/j.nicl.2019.102077

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