Chorea Associated with Genetic‐Confirmed CADASIL
Author:
Affiliation:
1. Department of Neurology, Parkinson Center Ajou University School of Medicine Suwon Republic of Korea
2. Department of Neurology Dongtan Sacred Heart Hospital Hallym University College of Medicine Hwaseong Republic of Korea
Funder
Ministry of Education
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Reference19 articles.
1. NOTCH3 Variants and Genotype-Phenotype Features in Chinese CADASIL Patients
2. Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: update on clinical, diagnostic, and management aspects
3. Vascular parkinsonism in a CADASIL case with an intact nigrostriatal dopaminergic system
4. First report of a pathogenic mutation on exon 24 of the NOTCH3 gene in a CADASIL family
5. Case Report: Progressive Asymmetric Parkinsonism Secondary to CADASIL Without Dementia
Cited by 3 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. Vascular Leukoencephalopathy Associated Chorea Due to A Heterozygous Htra 1 Variant: Novel Presentation of Cadasil Type II;Movement Disorders Clinical Practice;2024-08-06
2. Chorea Associated with Notch3 Gene Mutation;Movement Disorders Clinical Practice;2024-05-13
3. CADASIL: A NOTCH3-associated cerebral small vessel disease;Journal of Advanced Research;2024-01
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