CADASIL
Author:
Publisher
Elsevier
Reference99 articles.
1. New mutations in the Notch3 gene in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL);Abramycheva;J Neurol Sci,2015
2. Clinical spectrum of CADASIL and the effect of cardiovascular risk factors on phenotype: study in 200 consecutively recruited individuals;Adib-Samii;Stroke,2010
3. Hypomorphic Notch 3 alleles link Notch signaling to ischemic cerebral small-vessel disease;Arboleda-Velasquez;Proc Natl Acad Sci U S A,2011
4. Differential lesion patterns in CADASIL and sporadic subcortical arteriosclerotic encephalopathy: MR imaging study with statistical parametric group comparison;Auer;Radiology,2001
5. First deep intronic mutation in the NOTCH3 gene in a family with late-onset CADASIL;Bianchi;Neurobiology of Aging,2013
Cited by 53 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Novel mutation of NOTCH3 gene in a Chinese Patient with CADASIL: A case report;2024-08-26
2. Distinct neurological phenotypes associated with biallelic loss of NOTCH3 function: evidence for recessive inheritance;Molecular Biology Reports;2024-06-01
3. SNP and Structural Study of the Notch Superfamily Provides Insights and Novel Pharmacological Targets against the CADASIL Syndrome and Neurodegenerative Diseases;Genes;2024-04-23
4. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with multiple different onset forms of frequent recurrent attacks: A case report and literature review;Medicine;2024-03-15
5. Zerebrale Mikroangiopathien;InFo Neurologie + Psychiatrie;2024-03
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