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[Hereditary cerebral arteriopathy].

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke - 6 Nov 2003

Gustavsen W Rein, Eiklid Kristin

Abstract excerpt

CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy) is a neurovascular disease caused by mutations of the notch3 gene, manifesting with strokes or stroke-like episodes, psychiatric symptoms, migraine and dementia. The diagnosis can be confirmed by screening exons of this gene. Involvement of the anterior temporal lobe and external capsule on MRI and presence of...

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PMID: 14618173

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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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[Hereditary cerebral arteriopathy].PMID 14618173Read ↗

[The hereditary vessel disease CADASIL].Semantic proximity Read ↗

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[Clinical, radiological, histopathological and genetic findings in a Danish "CADASIL" family].Semantic proximity Read ↗

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CADASIL: hereditary disease of arteries causing brain infarcts and dementiaSemantic proximity Read ↗

[Clinical and neuroimaging findings in a family with CADASIL associated to C475T mutation].Semantic proximity Read ↗

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CADASIL.Semantic proximity Read ↗

[CADASIL].Semantic proximity Read ↗

[A study of subcortical infarcts and leukoencephalopathy (CADASIL) in a family with autosomal cerebral dominant arteriopathy].Semantic proximity Read ↗

[A new Spanish family with CADASIL associated with 346C>T mutation of NOTCH3 gene].Semantic proximity Read ↗

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

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