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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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| Publicado no: | Neuroimage Clin |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2019
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| Assuntos: | |
| 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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