When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference12 articles.
1. Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease;Hara;N Engl J Med,2009
2. A novel mutation of the high temperature requirement: a serine peptidase 1(HTRA1) gene in a Chinese family with cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL);Chen;J Int Med Res,2013
3. HTRA1-related cerebral small vessel disease: a review of the literature;Uemura;Front Neurol,2020
4. Shifting the CARASIL paradigm: report of a non-Asian family and literature review;Menezes Cordeiro;Stroke,2015
5. Two novel HTRA1 mutations in a European CARASIL patient;Bianchi;Neurology,2014
Cited by 1 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. Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy;Frontiers in Genetics;2023-09-18
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