First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy. - Wikidata - awgldk - TriplyDB

First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy.

First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy.

http://www.wikidata.org/entity/Q51819010

about

Pain as a channelopathy The Revolution in Migraine Genetics: From Aching Channels Disorders to a Next-Generation Medicine Migraine headache: a review of the molecular genetics of a common disorder The Relationship Between Headaches with Epileptic and Non-epileptic Seizures: a Narrative Review.Painful heat reveals hyperexcitability of the temporal pole in interictal and ictal migraine States The genetic relationship between epilepsy and hemiplegic migraine Headache, epilepsy and photosensitivity: how are they connected?Divergent sodium channel defects in familial hemiplegic migraine Early-onset familial hemiplegic migraine due to a novel SCN1A mutation.Subtype-selective targeting of voltage-gated sodium channels.Management of sporadic and familial hemiplegic migraine.Identification of molecular genetic factors that influence migraine.Migraine genes and the relation to gender.Human studies in the pathophysiology of migraine: genetics and functional neuroimaging.Pearls and pitfalls in genetic studies of migraine.Migraine genetics: Part II.Migraine and epilepsy: review of the literature.The borderland of migraine and epilepsy in children.Animal models of monogenic migraine.Spreading Depression in Primary and Secondary Headache Disorders.Epilepsy in hemiplegic migraine: Genetic mutations and clinical implications.Genetics of Migraine: Insights into the Molecular Basis of Migraine Disorders.Altered sleep regulation in a mouse model of SCN1A-derived genetic epilepsy with febrile seizures plus (GEFS+).Two novel SCN1A mutations identified in families with familial hemiplegic migraine.Migraine and preterm birth.Two novel families with hemiplegic migraine caused by recurrent SCN1A mutation p.F1499L.Seizure precipitants in a community-based epilepsy cohort.Familial hemiplegic migraine: A model for the genetic studies of migraine Familial hemiplegic migraine due to L263V SCN1A mutation: Discordance for epilepsy between two kindreds from Douro Valley Testing Genes Implicated in the Novel Case of Familial Hemiplegic Migraine

P2860

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P2860

First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy.

http://www.wikidata.org/entity/Q51819010

description

2009 nî lūn-bûn

@nan

2009年の論文

@ja

2009年学术文章

@wuu

2009年学术文章

@zh

2009年学术文章

@zh-cn

2009年学术文章

@zh-hans

2009年学术文章

@zh-my

2009年学术文章

@zh-sg

2009年學術文章

@yue

2009年學術文章

@zh-hant

name

First mutation in the voltage- ...... iplegic migraine and epilepsy.

@en

First mutation in the voltage- ...... iplegic migraine and epilepsy.

@nl

type

label

First mutation in the voltage- ...... iplegic migraine and epilepsy.

@en

First mutation in the voltage- ...... iplegic migraine and epilepsy.

@nl

prefLabel

First mutation in the voltage- ...... iplegic migraine and epilepsy.

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First mutation in the voltage- ...... iplegic migraine and epilepsy.

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J.1468-2982.2008.01721.X

P1433

P1476

First mutation in the voltage- ...... iplegic migraine and epilepsy.

@en

P2093

A H Stam

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

A M J M van den Maagdenberg

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B de Vries

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G M Terwindt

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J Barros

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J M Pereira-Monteiro

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K R J Vanmolkot

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M-J Castro

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R R Frants

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P2860

Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2

Neuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plus.

Noninactivating voltage-gated sodium channels in severe myoclonic epilepsy of infancy

A simple salting out procedure for extracting DNA from human nucleated cells

From ionic currents to molecular mechanisms: the structure and function of voltage-gated sodium channels

Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine

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

The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel

Nav1.1 mutations cause febrile seizures associated with afebrile partial seizures

Mutations of neuronal voltage-gated Na+ channel alpha 1 subunit gene SCN1A in core severe myoclonic epilepsy in infancy (SMEI) and in borderline SMEI (SMEB)

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308-313

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scholarly article

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10.1111/J.1468-2982.2008.01721.X

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3

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Michel D. Ferrari

Jorge Sequeiros

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2009-03-01T00:00:00Z

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19220312

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P921

migraine disorder