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Article

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

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology - 1 Apr 2002

Cevoli S, Pierangeli G, Monari L, Valentino M L, Bernardoni P, Mochi M, Cortelli P, Montagna P

Abstract excerpt

We describe an Italian family with familial hemiplegic migraine (FHM), subtle cerebellar signs and probable linkage to chromosome 1. FHM is genetically heterogeneous; in about 50% of families it is caused by mutations within the CACNA1A gene on chromosome 19. Linkage to 1q31 and 1g21-23 has also been established. Other families do not link either to chromosome 19 or 1. Chromosome 19-linked FHM may display...

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Identifiers

PMID: 12111614
DOI: 10.1007/s100720200016

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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

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Research trail→

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Familial hemiplegic migraine: clinical features and probable linkage to chromosome 1 in an Italian family.PMID 12111614Read ↗

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

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

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

Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23.Semantic proximity Read ↗

A new locus for hemiplegic migraine maps to chromosome 1q31.Semantic proximity Read ↗

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

A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxiaSemantic proximity Read ↗

Familial hemiplegic migraine: a ion channel disorder.Semantic proximity Read ↗

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

Wolff Award 1997. Involvement of a Ca2+ channel gene in familial hemiplegic migraine and migraine with and without aura. Dutch Migraine Genetics Research Group.Semantic proximity Read ↗

Chromosome 19p13 loci in Finnish migraine with aura families.Semantic proximity Read ↗

Genetic heterogeneity of familial hemiplegic migraine.Semantic proximity Read ↗

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