Patterns of gray matter atrophy in genetic frontotemporal dementia: results from the GENFI study

Frontotemporal dementia (FTD) is a highly heritable condition with multiple genetic causes. In this study, similarities and differences of gray matter (GM) atrophy patterns were assessed among 3 common forms of genetic FTD (mutations in C9orf72, GRN, and MAPT). Participants from the Genetic FTD Init...

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Publicat a:Neurobiol Aging
Autors principals: Cash, David M., Bocchetta, Martina, Thomas, David L., Dick, Katrina M., van Swieten, John C., Borroni, Barbara, Galimberti, Daniela, Masellis, Mario, Tartaglia, Maria Carmela, Rowe, James B., Graff, Caroline, Tagliavini, Fabrizio, Frisoni, Giovanni B., Laforce, Robert, Finger, Elizabeth, de Mendonça, Alexandre, Sorbi, Sandro, Rossor, Martin N., Ourselin, Sebastien, Rohrer, Jonathan D.
Format: Artigo
Idioma:Inglês
Publicat: Elsevier 2018
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5759893/
https://ncbi.nlm.nih.gov/pubmed/29172163
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neurobiolaging.2017.10.008
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