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- W2774743961 abstract "Background: Cerebral autosomal dominant arteriopathy with subcortical infarcts (CADASIL) is a hereditary small-vessel disease attributed to NOTCH3 gene mutation. Symptoms of CADASIL, including subcortical dementia, lacunar infarction, and white matter lesions, are associated with small cerebral arteries. Intracranial arterial stenosis (ICAS) is occasionally observed in CADASIL patients, although its etiology remains unknown." @default.
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- W2774743961 date "2017-10-01" @default.
- W2774743961 modified "2023-09-25" @default.
- W2774743961 title "Intracranial artery stenosis in Japanese CADASIL patients" @default.
- W2774743961 doi "https://doi.org/10.1016/j.jns.2017.08.3161" @default.
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