Associated Papers
Exploring the genetic frontier: Unraveling ANRIL, PAI-1, and HNF1α in stroke progression.
Hamadi A et al.
Plos One, 2025
Phenotypes Associated with NOTCH3 Cysteine-Sparing Mutations in Patients with Clinical Suspicion of CADASIL: A Systematic Review.
Cao Y et al.
International Journal of Molecular Sciences, 2024
Genetic Factors of Cerebral Small Vessel Disease and Their Potential Clinical Outcome.
Giau VV et al.
International Journal of Molecular Sciences, 2019
Vascular cognitive impairment associated with NOTCH3 Exon 33 mutation: A case report.
Sun Y et al.
Medicine, 2019
Systematic Review of Cysteine-Sparing NOTCH3 Missense Mutations in Patients with Clinical Suspicion of CADASIL.
Muiño E et al.
International Journal of Molecular Sciences, 2017
The Association Between the Genetic Variants of the NOTCH3 Gene and Ischemic Stroke Risk.
Yuan X et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research, 2016
Two novel mutations and a previously unreported intronic polymorphism in the NOTCH3 gene.
Roy B et al.
Mutation Research, 2012
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