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CADASIL

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
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Review Articles from PubMed

Review articles summarize what is currently known about a disease. They discuss research previously published by others. The terms "CADASIL" returned 12 free, full-text review articles. First few results:
CADASIL.
Last Updated: Aug 10, 2018

Cerebral small-vessel disease is a prevalent condition that is strongly associated with ischemic stroke and dementia. The most prevalent inherited cause of cerebral small-vessel disease is CADASIL, cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy, ...

Systematic Review of Cysteine-Sparing NOTCH3 Missense Mutations in Patients with Clinical Suspicion of CADASIL.
Last Updated: Dec 02, 2018

CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy) is caused by mutations in the gene, affecting the number of cysteines in the extracellular domain of the receptor, causing protein misfolding and receptor aggregation. The pathogenic ...

Recognizing CADASIL: a Secondary Cause of Migraine with Aura.
Last Updated: Nov 13, 2018

CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy) is an important disease to consider in the differential diagnosis of migraine with aura. This review examines current literature regarding migraine in CADASIL, as well as diagnostic ...

Full PubMed Review articles matches at NCBI:
12 Free Review Articles 53 Review Articles

Editorials from PubMed

Editorial articles describe the outcome of a single study. They are the published results of original research. The terms "CADASIL" returned 2 free, full-text editorial articles. First 2 results:
Full PubMed Editorials matches at NCBI:
2 Free Editorials 8 Editorials

Research Articles from PubMed

Research articles describe the outcome of a single study. They are the published results of original research. The terms "CADASIL" returned 136 free, full-text research articles. First few results:
The CADASIL Scale-J, A Modified Scale to Prioritize Access to Genetic Testing for Japanese CADASIL-Suspected Patients.
Last Updated: Jun 13, 2019

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is definitely diagnosed by genetic testing. Such testing involves the analysis of exons 2-24 of NOTCH3, which encode the epidermal growth factor-like repeat domain, where CADASIL mutations ...

A Novel NOTCH3 Gene Mutation in a Polish CADASIL Family.
Last Updated: Mar 14, 2019

Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) is a genetically determined disease of the cerebral vessels, characterized by recurrent ischemic strokes, dementia, and degeneration of the cerebral white matter. The condition is ...

3T MRI study discloses high intrafamilial variability in CADASIL due to a novel NOTCH3 mutation.
Last Updated: Dec 31, 2018

In order to evaluate the usefulness of presymptomatic MRI, we performed 3T brain MRI and Sanger gene sequencing in a proband with suspected but not confirmed CADASIL and her apparently asymptomatic father. The 35-year-old proband presented with migraine with visual aura. Brain MRI ...

Full PubMed Research articles matches at NCBI:
136 Free Research Articles 537 Research Articles