Migraine and epilepsy: genetically linked? - Wikidata - awgldk - TriplyDB

Migraine and epilepsy: genetically linked?

Migraine and epilepsy: genetically linked?

http://www.wikidata.org/entity/Q34657045

about

Benign mesial temporal lobe epilepsy.

P2860

Q44054641-16A9D02E-81EA-4DB7-B233-564896654B07

P2860

Migraine and epilepsy: genetically linked?

http://www.wikidata.org/entity/Q34657045

description

2008 nî lūn-bûn

@nan

2008 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2008年の論文

@ja

2008年論文

@yue

2008年論文

@zh-hant

2008年論文

@zh-hk

2008年論文

@zh-mo

2008年論文

@zh-tw

2008年论文

@wuu

name

Migraine and epilepsy: genetically linked?

@ast

Migraine and epilepsy: genetically linked?

@en

Migraine and epilepsy: genetically linked?

@nl

type

label

Migraine and epilepsy: genetically linked?

@ast

Migraine and epilepsy: genetically linked?

@en

Migraine and epilepsy: genetically linked?

@nl

prefLabel

Migraine and epilepsy: genetically linked?

@ast

Migraine and epilepsy: genetically linked?

@en

Migraine and epilepsy: genetically linked?

@nl

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Q34657045-8C5702E3-A257-48F2-BCEC-8154D44FBBD9

P356

14737175.8.9.1307

P1433

Expert Review of Neurotherapeutics: a key contribution to decision making in the treatment of neurologic and neuropsychiatric disorders

P1476

Migraine and epilepsy: genetically linked?

@en

P2093

Joost Haan

http://www.w3.org/2001/XMLSchema#string

Oebele F Brouwer

http://www.w3.org/2001/XMLSchema#string

P2860

Mechanisms of migraine aura revealed by functional MRI in human visual cortex

Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions

A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression

Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine

Suppression of cortical spreading depression in migraine prophylaxis

Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy

Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation

Impaired neurotransmitter release and elevated threshold for cortical spreading depression in mice with mutations in the alpha1A subunit of P/Q type calcium channels

The ataxic groggy rat has a missense mutation in the P/Q-type voltage-gated Ca2+ channel alpha1A subunit gene and exhibits absence seizures.

Migraine with aura is a risk factor for unprovoked seizures in children.

P304

1307-1311

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scholarly article

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10.1586/14737175.8.9.1307

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9

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8

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P50

Michel D. Ferrari

Arn van den Maagdenberg

P577

2008-09-01T00:00:00Z

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18759542

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P921

migraine disorder