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Article

Childhood-onset CADASIL: clinical, imaging, and neurocognitive features.

Journal of child neurology - 1 May 2010

Hartley Jessica, Westmacott Robyn, Decker Jochen, Shroff Manohar, Yoon Grace

Abstract excerpt

CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy) is a progressive neurodegenerative condition, associated with mutations in the notch3 gene. Symptoms include migraine with aura, mood disorders, progressive cognitive decline, subcortical ischemic...

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Source

Identifiers

PMID: 20197270
DOI: 10.1177/0883073810361382

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20197270-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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Childhood-onset CADASIL: clinical, imaging, and neurocognitive features.PMID 20197270Read ↗

CADASIL: neuropsychological findings in three generations of an affected family.Semantic proximity Read ↗

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Genetically proven cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) in a 3-year-old.Semantic proximity Read ↗

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Comparison of clinical, familial, and MRI features of CADASIL and NOTCH3-negative patients.Semantic proximity Read ↗

CADASIL.Semantic proximity Read ↗

Early-Onset Vascular Leukoencephalopathy Caused by Bi-Allelic NOTCH3 Variants.Semantic proximity Read ↗

A Novel Heterozygous Variant in Exon 19 of NOTCH3 in a Saudi Family with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy.Semantic proximity Read ↗

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An unusual case of elderly-onset cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with multiple cerebrovascular risk factors.Semantic proximity Read ↗

Clinical presentation of CADASIL in an Italian patient with a rare Gly528Cys exon 10 NOTCH3 gene mutation.Semantic proximity Read ↗

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