P/Q-type Ca2+ channel defects in migraine, ataxia and epilepsy. (Q45934932)

18 December 2017

review article

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title

P/Q-type Ca2+ channel defects in migraine, ataxia and epilepsy. (English)

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18 December 2017

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4

Ferrari MD

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18 December 2017

Ophoff RA

1

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18 December 2017

Terwindt GM

series ordinal

2

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18 December 2017

Frants RR

series ordinal

3

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18 December 2017

publication date

1 April 1998

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18 December 2017

Trends in Pharmacological Sciences

published in

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18 December 2017

volume

19

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18 December 2017

issue

4

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18 December 2017

page(s)

121-127

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18 December 2017

Calcium channel diversity and neurotransmitter release: the omega-conotoxins and omega-agatoxins

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Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

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Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19p

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Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p

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7 January 2021

Molecular features of the CAG repeats of spinocerebellar ataxia 6 (SCA6)

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7 January 2021

The expanding world of trinucleotide repeats

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7 January 2021

Absence epilepsy in tottering mutant mice is associated with calcium channel defects

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Inherited epilepsy: spike-wave and focal motor seizures in the mutant mouse tottering

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Mutations in the Cacnl1a4 calcium channel gene are associated with seizures, cerebellar degeneration, and ataxia in tottering and leaner mutant mice

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7 January 2021

Comorbidity of migraine and epilepsy

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7 January 2021

Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse.

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7 January 2021

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7 January 2021

Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura

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7 January 2021

Dual function of the voltage-dependent Ca2+ channel alpha 2 delta subunit in current stimulation and subunit interaction.

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7 January 2021

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Identifiers

DOI

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18 December 2017

PubMed ID

9612085

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18 December 2017