Cargando…
The Role of White Matter Dysfunction and Leukoencephalopathy/Leukodystrophy Genes in the Aetiology of Frontotemporal Dementias: Implications for Novel Approaches to Therapeutics
Frontotemporal dementia (FTD) is a common cause of presenile dementia and is characterized by behavioural and/or language changes and progressive cognitive deficits. Genetics is an important component in the aetiology of FTD, with positive family history of dementia reported for 40% of cases. This r...
Autores principales: | Lok, Hiu Chuen, Kwok, John B. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7961524/ https://www.ncbi.nlm.nih.gov/pubmed/33802612 http://dx.doi.org/10.3390/ijms22052541 |
Ejemplares similares
-
Profiles of white matter tract pathology in frontotemporal dementia
por: Mahoney, Colin J., et al.
Publicado: (2014) -
Elevated GRO-α and IL-18 in serum and brain implicate the NLRP3 inflammasome in frontotemporal dementia
por: Lok, Hiu Chuen, et al.
Publicado: (2023) -
ATP-binding cassette transporter expression is widely dysregulated in frontotemporal dementia with TDP-43 inclusions
por: Katzeff, Jared S., et al.
Publicado: (2022) -
Longitudinal Grey and White Matter Changes in Frontotemporal Dementia and Alzheimer’s Disease
por: Frings, Lars, et al.
Publicado: (2014) -
Functional connectivity and microstructural white matter changes in phenocopy frontotemporal dementia
por: Meijboom, R., et al.
Publicado: (2016)