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Article

A case report about CADASlL: mutation in the NOTCH 3 receptor.

Acta neurologica Taiwanica - 1 Dec 2009

Delibas Sennur, Guven Hayat, Comoglu Selim Selcuk

Abstract excerpt

CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy) is a rare autosomal dominant genetic disease characterized with recurrent stroke, migrainous headache, cognitive deficits, and psychiatric symptoms associated with mutations in the NOTCH 3 gene on chromosome 19. Here, we report a case of CADASIL who presented with migrainous headache, behavioral disorder, and...

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PMID: 20329594

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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A case report about CADASlL: mutation in the NOTCH 3 receptor.PMID 20329594Read ↗

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

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A new de novo Notch3 mutation causing CADASIL.Semantic proximity Read ↗

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Unusual clinical presentations in subjects carrying novel NOTCH3 gene mutations.Semantic proximity Read ↗

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