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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Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5759893/
https://www.ncbi.nlm.nih.gov/pubmed/29172163
http://dx.doi.org/10.1016/j.neurobiolaging.2017.10.008

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5759893/
https://www.ncbi.nlm.nih.gov/pubmed/29172163
http://dx.doi.org/10.1016/j.neurobiolaging.2017.10.008

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