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Article

Investigating the association between Notch3 polymorphism and migraine.

Headache - 1 Feb 2006

Borroni Barbara, Brambilla Cristina, Liberini Paolo, Rao Renata, Archetti Silvana, Venturelli Elisabetta, Gipponi Stefano, Caimi Luigi, Padovani Alessandro

Abstract excerpt

OBJECTIVE: The aim of the present study was to evaluate whether the functional Notch3 polymorphism T6746C, which is not causative for cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), might be a risk factor for migraine. BACKGROUND: It has been recently demonstrated that migraine is characterized by subclinical brain infarctions and white matter lesions. Several...

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Source

Identifiers

PMID: 16492242
DOI: 10.1111/j.1526-4610.2006.00344.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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Investigating the association between Notch3 polymorphism and migraine.PMID 16492242Read ↗

Association of a Notch 3 gene polymorphism with migraine susceptibility.Semantic proximity Read ↗

Genetic variants of the NOTCH3 gene in migraine--a mutation analysis and association study.Semantic proximity Read ↗

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Clinical presentation of Y189C mutation of the NOTCH3 gene in the Polish family with CADASIL.Semantic proximity Read ↗

APOE and AGT in the Finnish p.Arg133Cys CADASIL population.Semantic proximity Read ↗

Two novel Italian CADASIL families from Central Italy with mutation CGC-TGC at codon 1006 in the exon 19 Notch3 gene.Semantic proximity Read ↗

Recognition of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) in Two Oligosymptomatic Sisters with Low CADASIL Scale Scores and a Venous Dysplasia: Report of a Novel Greek Family.Semantic proximity Read ↗

Genetic and nongenetic factors associated with CADASIL: A retrospective cohort study.Semantic proximity Read ↗

Mutational and haplotype map of NOTCH3 in a cohort of Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).Semantic proximity Read ↗

De novo mutation in the NOTCH3 gene causing CADASIL.Semantic proximity Read ↗

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy and right-to-left shunt: lack of evidence for an association in a prevalence study.Semantic proximity Read ↗

NOTCH3 gene mutations in subjects clinically suspected of CADASIL.Semantic proximity Read ↗

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