The genetic spectrum and the evaluation of CADASIL screening scale in Chinese patients with NOTCH3 mutations-Reference-Cited by-同舟云学术

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The genetic spectrum and the evaluation of CADASIL screening scale in Chinese patients with NOTCH3 mutations

Published:2015-07 Issue:1-2 Volume:354 Page:63-69
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Liu Xiao,Zuo Yuehuan,Sun Wei,Zhang Wei,Lv He,Huang Yining,Xiao Jiangxi,Yuan Yun,Wang Zhaoxia

Funder

National Natural Science Foundation of China

Ministry of Science and Technology of China

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference28 articles.

1. CADASIL;Hervé;J Geriatr Psychiatry Neurol,2010

2. NOTCH3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia;Joutel;Nature,1996

3. CADASIL and CARASIL;Tikka;Brain Pathol,2014

4. Characteristics of CADASIL in Chinese mainland patients;Tan;Neurol India,2014

5. Peripheral artery disease as a manifestation of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) and practical implications;Briceno;Circulation,2013

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1. Phenotypes Associated with NOTCH3 Cysteine-Sparing Mutations in Patients with Clinical Suspicion of CADASIL: A Systematic Review;International Journal of Molecular Sciences;2024-08-13

2. Sex differences in frontotemporal atrophy in CADASIL revealed by 7-Tesla MRI;NeuroImage: Clinical;2023

3. Update on the Epidemiology, Pathogenesis, and Biomarkers of Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy;Journal of Clinical Neurology;2023

4. Three-tiered EGFr domain risk stratification for individualized NOTCH3-small vessel disease prediction;Brain;2022-12-20

5. Exome-based gene panel analysis in a cohort of acute juvenile ischemic stroke patients:relevance of NOTCH3 and GLA variants;Journal of Neurology;2022-11-21

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