Associated Papers
CADASIL: A NOTCH3-associated cerebral small vessel disease.
Yuan L et al.
Journal of Advanced Research, 2024
38176524 (PubMed )
Supplement: mmc1.doc
Systematic Review of Cerebral Phenotypes Associated With Monogenic Cerebral Small-Vessel Disease.
Whittaker E et al.
Journal of the American Heart Association, 2022
Whole-exome sequencing reveals a role of HTRA1 and EGFL8 in brain white matter hyperintensities.
Malik R et al.
Brain : a Journal of Neurology, 2021
Heterozygous mutations of HTRA1 gene in patients with familial cerebral small vessel disease.
Di Donato I et al.
Cns Neuroscience & Therapeutics, 2017
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