Cargando…
Systematic Review of Cerebral Phenotypes Associated With Monogenic Cerebral Small‐Vessel Disease
BACKGROUND: Cerebral small‐vessel disease (cSVD) is an important cause of stroke and vascular dementia. Most cases are multifactorial, but an emerging minority have a monogenic cause. While NOTCH3 is the best‐known gene, several others have been reported. We aimed to summarize the cerebral phenotype...
Autores principales: | Whittaker, Ed, Thrippleton, Sophie, Chong, Liza Y. W., Collins, Victoria G., Ferguson, Amy C., Henshall, David E., Lancastle, Emily, Wilkinson, Tim, Wilson, Blair, Wilson, Kirsty, Sudlow, Cathie, Wardlaw, Joanna, Rannikmäe, Kristiina |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9238640/ https://www.ncbi.nlm.nih.gov/pubmed/35699195 http://dx.doi.org/10.1161/JAHA.121.025629 |
Ejemplares similares
-
Frequency and Phenotype Associations of Rare Variants in 5 Monogenic Cerebral Small Vessel Disease Genes in 200,000 UK Biobank Participants
por: Ferguson, Amy Christina, et al.
Publicado: (2022) -
Benchmarking network-based gene prioritization methods for cerebral small vessel disease
por: Zhang, Huayu, et al.
Publicado: (2021) -
Advanced Neuroimaging of Cerebral Small Vessel Disease
por: Blair, Gordon W., et al.
Publicado: (2017) -
Enlarged perivascular spaces and cerebral small vessel disease
por: Potter, Gillian M, et al.
Publicado: (2015) -
Stem cell treatment and cerebral palsy: Systemic review and meta-analysis
por: Eggenberger, Simone, et al.
Publicado: (2019)