Articles with "patients cadasil" as a keyword



Abstract TMP67: Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy May Affect Large Cerebral Arteries

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Published in 2024 at "Stroke"

DOI: 10.1161/str.55.suppl_1.tmp67

Abstract: Introduction: CADASIL is the most common monogenic small-vessel disease (SVD) form. Large and small brain arteries are intimately related, but it is unclear whether people with CADASIL have changes in their large arteries as a… read more here.

Keywords: tmp67 cerebral; abstract tmp67; large arteries; patients cadasil ... See more keywords

Prevalence and Predictors of Vascular Cognitive Impairment in Patients With CADASIL

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Published in 2022 at "Neurology"

DOI: 10.1212/wnl.0000000000200607

Abstract: Background and Objectives Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most common monogenic form of stroke and early-onset dementia. We determined the prevalence of vascular cognitive impairment (VCI) in a… read more here.

Keywords: vci; patients cadasil; prevalence; vascular cognitive ... See more keywords

Determining Clinical Disease Progression in Symptomatic Patients With CADASIL

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Published in 2024 at "Neurology"

DOI: 10.1212/wnl.0000000000210193

Abstract: Background and Objectives Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most frequent small artery brain disease caused by pathogenic variants of the NOTCH3 gene. During the disease, we still do… read more here.

Keywords: disease; determining clinical; progression; clinical disease ... See more keywords

Reduced macular vessel density and inner retinal thickness correlate with the severity of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

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Published in 2022 at "PLoS ONE"

DOI: 10.1371/journal.pone.0268572

Abstract: Background Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), caused by mutations in NOTCH3, is the most common cause of hereditary cerebral small vessel disease. Whether it will involve systemic vasculopathy such as… read more here.

Keywords: patients cadasil; density; retinal thickness; vessel density ... See more keywords