Altered Default Mode Network Is Associated With Cognitive Impairment in CADASIL as Revealed by Multimodal Neuroimaging

Background and Purpose: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy caused by mutations in the NOTCH3 gene is a hereditary cerebral small vessel disease, manifesting with stroke, cognitive impairment, and mood disturbances. Functional or structural chan...

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Detalles Bibliográficos
Autores principales: Li, Panlong, Huang, Qi, Ban, Shiyu, Qiao, Yuan, Wu, Jing, Zhai, Yu, Du, Xiaoxia, Hua, Fengchun, Su, Jingjing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8685443/
https://www.ncbi.nlm.nih.gov/pubmed/34938255
http://dx.doi.org/10.3389/fneur.2021.735033

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8685443/
https://www.ncbi.nlm.nih.gov/pubmed/34938255
http://dx.doi.org/10.3389/fneur.2021.735033

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