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

Familial hemiplegic migraine: a clinical comparison of families linked and unlinked to chromosome 19.DMG RG.

Cephalalgia : an international journal of headache - 1 May 1996

Terwindt G M, Ophoff R A, Haan J, Frants R R, Ferrari M D

Abstract excerpt

We compared the clinical characteristics of 46 patients from three unrelated families with familial hemiplegic migraine (FHM) linked to chromosome 19, with those of 20 patients from two families with FHM not linked to chromosome 19. We found no significant differences for age at onset, frequency and duration of attacks, duration of the paresis, and occurrence of basilar migraine symptoms. In the linked families,...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Child
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 19

Share to Genetic Linkage

Share to Genotype

Share to Migraine Disorders

Share to Phenotype

Source

Identifiers

PMID: 8734765
DOI: 10.1046/j.1468-2982.1996.1603153.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Familial hemiplegic migraine: a clinical comparison of families linked and unlinked to chromosome 19.DMG RG.PMID 8734765Read ↗

Familial hemiplegic migraine: clinical features and probable linkage to chromosome 1 in an Italian family.Semantic proximity Read ↗

Familial migraine: exclusion of the susceptibility gene from the reported locus of familial hemiplegic migraine on 19p.Semantic proximity Read ↗

Mapping of a second locus for familial hemiplegic migraine to 1q21–q23 and evidence of further heterogeneitySemantic proximity Read ↗

Genetic heterogeneity of familial hemiplegic migraine.Semantic proximity Read ↗

[Familial hemiplegic migraine. Localization of a responsible gene on chromosome 19].Semantic proximity Read ↗

Familial Hemiplegic Migraine and Recurrent Episodes of Psychosis: A Case Report.Semantic proximity Read ↗

Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus.Semantic proximity Read ↗

A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p.Semantic proximity Read ↗

Familial episodic ataxia: Clinical heterogeneity in four families linked to chromosome 19pSemantic proximity Read ↗

Familial typical migraineSemantic proximity Read ↗

Clinical spectrum in three families with familial hemiplegic migraine type 2 including a novel mutation in the ATP1A2 gene.Semantic proximity Read ↗

Genetic heterogeneity in Italian families with familial hemiplegic migraineSemantic proximity Read ↗

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