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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 13 free, full-text review articles. First few results:
CADASIL: new advances in basic science and clinical perspectives.
Last Updated: Jul 02, 2020

Recent advances in genetic evaluation improved the identification of several variants in the NOTCH3 gene causing Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL). Despite improved diagnosis, the disease mechanism remains an elusive ...

Clinical and research applications of magnetic resonance imaging in the study of CADASIL.
Last Updated: Apr 17, 2020

Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) is an inherited small vessel disease that leads to early cerebrovascular events and functional disability. It is the most common single-gene disorder leading to stroke. Magnetic resonance ...

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, ...

Full PubMed Review articles matches at NCBI:
13 Free Review Articles 56 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 3 free, full-text editorial articles. First few results:
Full PubMed Editorials matches at NCBI:
3 Free Editorials 10 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 155 free, full-text research articles. First few results:
Homozygous NOTCH3 p.R587C mutation in Chinese patients with CADASIL: a case report.
Last Updated: Jul 23, 2020

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited small vessel disease caused by mutations in NOTCH3 gene with remarkable phenotypic heterogeneity. Cases of CADASIL associated with homozygous NOTCH3 mutations are rare ...

Reduced resting-state brain functional network connectivity and poor regional homogeneity in patients with CADASIL.
Last Updated: Feb 10, 2020

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) manifests principally as a suite of cognitive impairments, particularly in the executive domain. Executive functioning requires the dynamic coordination of neural activity over large-scale ...

A Cross-Sectional Analysis of Migraine-Related Disability in CADASIL: A Mayo Clinic Cohort.
Last Updated: May 01, 2020

Cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is inherited microangiopathy characterized by recurrent subcortical infarcts. A majority of those with CADASIL report coexistent migraine with aura. The authors aim to quantitatively ...

Full PubMed Research articles matches at NCBI:
155 Free Research Articles 581 Research Articles