Mechanisms regulating cerebral hypoperfusion in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

Cerebral small vessel disease (CSVD) is a leading cause of stroke and dementia. As the most common type of inherited CSVD, cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is characterized by the NOTCH3 gene mutation which leads to Notch3 ectodomai...

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Detalles Bibliográficos
Autores principales: Yan, Xi, Shang, Junkui, Wang, Runrun, Wang, Fengyu, Zhang, Jiewen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial Department of Journal of Biomedical Research 2022
Materias:
Mini-Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9548441/
https://www.ncbi.nlm.nih.gov/pubmed/36165325
http://dx.doi.org/10.7555/JBR.36.20220208

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9548441/
https://www.ncbi.nlm.nih.gov/pubmed/36165325
http://dx.doi.org/10.7555/JBR.36.20220208

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