Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Phenotypic and genetic analysis of a large family with migraine-associated vertigo.

Headache - 1 Jan 2000

Lee Hane, Jen Joanna C, Cha Yoon-Hee, Nelson Stanley F, Baloh Robert W

Abstract excerpt

OBJECTIVES: To describe a large multigenerational family with migraine-associated vertigo (MAV) combining a detailed phenotypic and genetic analysis. BACKGROUND: Migraine-associated vertigo is said to be highly prevalent in the general population and, like other migraine syndromes, its etiology is felt to have a strong genetic component. However, so far, there have been no reports of large families with MAV....

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Brain Chemistry
Share to Chromosome Mapping
Share to Chromosomes, Human, Pair 11

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Mutational Analysis

Share to Genetic Testing

Share to Inheritance Patterns

Share to Migraine Disorders

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 18081823
DOI: 10.1111/j.1526-4610.2007.01002.x
PMCID: PMC2846425

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 11 closest

Phenotypic and genetic analysis of a large family with migraine-associated vertigo.PMID 18081823Read ↗

A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity.Semantic proximity Read ↗

Locus for Familial Migrainous Vertigo Disease Maps to Chromosome 5q35Semantic proximity Read ↗

Migrainous vertigo: mutation analysis of the candidate genes CACNA1A, ATP1A2, SCN1A, and CACNB4.Semantic proximity Read ↗

Association of progesterone receptor with migraine-associated vertigo.Semantic proximity Read ↗

Familial clustering of migraine, episodic vertigo, and Ménière's disease.Semantic proximity Read ↗

Familial benign recurrent vertigoSemantic proximity Read ↗

Migraine and vasodepressor syncope in a large family.Semantic proximity Read ↗

Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenonSemantic proximity Read ↗

Localization of a gene for migraine without aura to chromosome 4q21.Semantic proximity Read ↗

A susceptibility locus for migraine with aura, on chromosome 4q24.Semantic proximity Read ↗

Familial migraine with vertigo: no mutations found in CACNA1A.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.