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Article

A novel CADASIL-causing mutation in a stroke patient.

Swiss medical weekly - 2 Jun 2007

Vikelis Michail, Papatriantafyllou John, Karageorgiou Clementine E

Abstract excerpt

BACKGROUND: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) is an uncommon autosomal dominant genetic disease due to mutations in the Notch3 gene on chromosome 19. The major clinical characteristics of CADASIL are migraine, recurrent ischaemic strokes and dementia. CASE REPORT: We describe the case of a 58-year old man who presented with a minor stroke that...

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Source

Identifiers

PMID: 17629811
DOI: 10.4414/smw.2007.11816

Provenance

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

Source receipt: pubmed, retrieved 7 Sept 2026.

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A novel CADASIL-causing mutation in a stroke patient.PMID 17629811Read ↗

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