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Article

Japanese cases of familial hemiplegic migraine with cerebellar ataxia carrying a T666M mutation in the CACNA1A gene.

Journal of neurology, neurosurgery, and psychiatry - 1 May 2002

Takahashi T, Igarashi S, Kimura T, Hozumi I, Kawachi I, Onodera O, Takano H, Saito M, Tsuji S

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Share to Calcium Channels
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Share to Chromosomes, Human, Pair 19
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Tomography, Emission-Computed, Single-Photon

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Identifiers

PMID: 11971066
DOI: 10.1136/jnnp.72.5.676-a
PMCID: PMC1737889

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

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Research trail→

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Japanese cases of familial hemiplegic migraine with cerebellar ataxia carrying a T666M mutation in the CACNA1A gene.PMID 11971066Read ↗

Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation.Semantic proximity Read ↗

Wide clinical variability in a family with a CACNA1A T666m mutation: hemiplegic migraine, coma, and progressive ataxia.Semantic proximity Read ↗

Progressive Ataxia with Hemiplegic Migraines: a Phenotype of CACNA1A Missense Mutations, Not CAG Repeat Expansions.Semantic proximity Read ↗

CACNA1A-p.Thr501Met mutation associated with familial hemiplegic migraine: a family report.Semantic proximity Read ↗

CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy.Semantic proximity Read ↗

New CACNA1A gene mutation in a case of familial hemiplegic migraine with status epilepticus.Semantic proximity Read ↗

The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.Semantic proximity Read ↗

Cerebellar ataxia, hemiplegic migraine, and related phenotypes due to a CACNA1A missense mutation: 12-year follow-up of a large Portuguese family.Semantic proximity Read ↗

Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4Semantic proximity Read ↗

CACNA1A Gene Variants in Eight Chinese Patients With a Wide Range of PhenotypesSemantic proximity Read ↗

Familial hemiplegic migraine.Semantic proximity Read ↗

CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine.Semantic proximity Read ↗

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