Interpretation ofNOTCH3mutations in the diagnosis of CADASIL-Reference-Cited by-同舟云学术

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Interpretation ofNOTCH3mutations in the diagnosis of CADASIL

Published:2014-05-21 Issue:5 Volume:14 Page:593-603
ISSN:1473-7159
Container-title:Expert Review of Molecular Diagnostics
language:en
Short-container-title:Expert Review of Molecular Diagnostics

Author:

Rutten Julie W,Haan Joost,Terwindt Gisela M,van Duinen Sjoerd G,Boon Elles MJ,Lesnik Oberstein Saskia AJ

Publisher

Informa UK Limited

Subject

Genetics,Molecular Biology,Molecular Medicine,Pathology and Forensic Medicine

Link

http://www.tandfonline.com/doi/pdf/10.1586/14737159.2014.922880

Reference94 articles.

1. Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy.

2. Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study.

3. Clinical spectrum of CADASIL: a study of 7 families

4. Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

5. The minimum prevalence of CADASIL in northeast England

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1. Clinical and neuroradiological spectrum of biallelic variants in NOTCH3;eBioMedicine;2024-09

2. Association of NOTCH3 Variant Risk Category With 2-Year Clinical and Radiologic Small Vessel Disease Progression in Patients With CADASIL;Neurology;2024-05-28

3. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy presenting as recurrent stroke and ataxia;BMJ Case Reports;2024-05

4. Progress in the Study of the Role and Mechanism of HTRA1 in Diseases Related to Vascular Abnormalities;International Journal of General Medicine;2024-04

5. Stroke genetics and how it Informs novel drug discovery;Expert Opinion on Drug Discovery;2024-03-04

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