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- [21] A Novel Heterozygous Variant in Exon 19 of NOTCH3 in a Saudi Family with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy JOURNAL OF STROKE & CEREBROVASCULAR DISEASES, 2020, 29 (07):
- [23] Effects of Lacunar Infarctions on Cognitive Impairment in Patients with Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy JOURNAL OF CLINICAL NEUROLOGY, 2011, 7 (04): : 210 - 214
- [25] Evaluation of NOTCH3 Pro167Ser Variation in a Japanese Family with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy DEMENTIA AND GERIATRIC COGNITIVE DISORDERS EXTRA, 2016, 6 (02): : 183 - +
- [26] Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementia CEREBROVASCULAR PATHOLOGY IN ALZHEIMER'S DISEASE, 1997, 826 : 213 - 217
- [28] Transgenic mice expressing mutant Notch3 develop vascular alterations characteristic of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy AMERICAN JOURNAL OF PATHOLOGY, 2003, 162 (01): : 329 - 342
- [30] Genetically proven cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) in a 3-year-old Pediatric Radiology, 2013, 43 : 1227 - 1230