Cargando…
Resting State Functional Connectivity Is Decreased Globally Across the C9orf72 Mutation Spectrum
A repeat expansion mutation in the C9orf72 gene causes amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTD), or symptoms of both, and has been associated with gray and white matter changes in brain MRI scans. We used graph theory to examine the network properties of brain function at r...
Autores principales: | Smallwood Shoukry, Rachel F., Clark, Michael G., Floeter, Mary Kay |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710968/ https://www.ncbi.nlm.nih.gov/pubmed/33329355 http://dx.doi.org/10.3389/fneur.2020.598474 |
Ejemplares similares
-
Longitudinal changes in resting state networks in early presymptomatic carriers of C9orf72 expansions
por: Shoukry, Rachel Smallwood, et al.
Publicado: (2020) -
Biomarkers for Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Associated With Hexanucleotide Expansion Mutations in C9orf72
por: Floeter, Mary Kay, et al.
Publicado: (2018) -
The repeat length of C9orf72 is associated with the survival of amyotrophic lateral sclerosis patients without C9orf72 pathological expansions
por: Tang, Lu, et al.
Publicado: (2022) -
Analysis of Heritability Across the Clinical Phenotypes of Frontotemporal Dementia and the Frequency of the C9ORF72 in a Colombian Population
por: López-Cáceres, Andrea, et al.
Publicado: (2021) -
Longitudinal imaging in C9orf72 mutation carriers: Relationship to phenotype
por: Floeter, Mary Kay, et al.
Publicado: (2016)