A case of leukoencephalopathy and small vessels disease caused by a novel HTRA1 homozygous mutation

T Gündüz, Y Demirkol, Ö Doğan, S Demir… - Journal of Stroke and …, 2019 - Elsevier
Cerebral autosomal recessive arteriopathy with subcortical infarcts and
leukoencephalopathy (CARASIL) is a heritable, rare small vessel disease, which is caused …

[HTML][HTML] A novel mutation in the HTRA1 gene identified in Chinese CARASIL pedigree

XL Wang, CF Li, HW Guo, BZ Cao - CNS neuroscience & …, 2012 - ncbi.nlm.nih.gov
Cerebral autosomal recessive arteriopathy with subcortical infarcts and
leukoencephalopathy (CARASIL) is an inherited autosomal recessive vascular diseases …

Cerebral small vessel disease due to a unique heterozygous HTRA1 mutation in an African man

OJ Oluwole, H Ibrahim, D Garozzo… - Neurology …, 2019 - AAN Enterprises
Objective To describe the case of an African patient who was diagnosed with cerebral
autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy …

Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy

YM Li, W Jia, T Xin, YQ Fang - Frontiers in Genetics, 2023 - frontiersin.org
Background: Cerebral autosomal recessive arteriopathy with subcortical infarcts and
leukoencephalopathy (CARASIL) is an autosomal recessive disorder characterized by …

Shifting the CARASIL paradigm: report of a non-Asian family and literature review

I Menezes Cordeiro, H Nzwalo, F Sá, RB Ferreira… - Stroke, 2015 - Am Heart Assoc
Background and Purpose—Cerebral autosomal recessive arteriopathy with subcortical
infarcts and leukoencephalopathy (CARASIL) is a rare form of nonhypertensive cerebral …

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): from discovery to gene identification

T Fukutake - Journal of Stroke and Cerebrovascular Diseases, 2011 - Elsevier
Cerebral autosomal recessive arteriopathy with subcortical infarcts and
leukoencephalopathy (CARASIL) is a single-gene disorder directly affecting the cerebral …

Genetically confirmed CARASIL: Case report with novel HTRA1 mutation and literature review

Z Yu, S Cao, A Wu, H Yue, C Zhang, J Wang, M Xia… - World neurosurgery, 2020 - Elsevier
Background Cerebral autosomal recessive arteriopathy with subcortical infarcts and
leukoencephalopathy (CARASIL) is an extremely rare monogenic autosomal disease …

Histopathologic analysis of cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): a report of a new genetically …

S Ito, M Takao, T Fukutake, H Hatsuta… - … of Neuropathology & …, 2016 - academic.oup.com
Cerebral autosomal recessive arteriopathy with subcortical infarcts and
leukoencephalopathy (CARASIL) is a nonhypertensive hereditary cerebral small vessel …

Novel mutation of HTRA1 gene causes cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy: one case

W LI, D Zhao, Z Wang, D Hong… - Chinese Journal of …, 2012 - pesquisa.bvsalud.org
ObjectiveTo report a novel HTRA1 gene mutation caused cerebral autosomal recessive
arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL) with migraine …

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): A challenging diagnosis and a rare multiple sclerosis mimic

B Shirah, H Algahtani, R Algahtani, A Alfares… - Journal of Stroke and …, 2023 - Elsevier
Cerebral autosomal recessive arteriopathy with subcortical infarcts and
leukoencephalopathy (CARASIL) is an extremely rare hereditary cerebral small vessel …