A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs - Wikidata - awgldk - TriplyDB

A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs

A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs

http://www.wikidata.org/entity/Q28285675

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The cerebellum and migraine 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 Glutamate-system defects behind psychiatric manifestations in a familial hemiplegic migraine type 2 disease-mutation mouse model.A novel ATP1A2 mutation in a family with FHM type II Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine Increased susceptibility to cortical spreading depression in the mouse model of familial hemiplegic migraine type 2.Migraine: new molecular mechanisms.Familial hemiplegic migraine.Clinical and neuroimaging evidence of interictal cerebellar dysfunction in FHM2.Migraine genetics.Prolonged hemiplegic episodes in children due to mutations in ATP1A2.Psychotic aura symptoms in familial hemiplegic migraine type 2 (ATP1A2)Intravenous nimodipine worsening prolonged attack of familial hemiplegic migraine.Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3 The primary headaches: genetics, epigenetics and a behavioural genetic model.Current trends in migraine prophylaxis.Acute encephalopathy in familial hemiplegic migraine with ATP1A2 mutation.The structure of the Na+,K+-ATPase and mapping of isoform differences and disease-related mutations.Familial Hemiplegic Migraine with Severe Attacks: A New Report with ATP1A2 Mutation.Novel mutations affecting the Na, K ATPase alpha model complex neurological diseases and implicate the sodium pump in increased longevity.Management of sporadic and familial hemiplegic migraine.Migraine genes and the relation to gender.Genetic effects of ATP1A2 in familial hemiplegic migraine type II and animal models.The α2β2 isoform combination dominates the astrocytic Na(+) /K(+) -ATPase activity and is rendered nonfunctional by the α2.G301R familial hemiplegic migraine type 2-associated mutation.Animal models of monogenic migraine.Epilepsy in hemiplegic migraine: Genetic mutations and clinical implications.Diverse functional consequences of mutations in the Na+/K+-ATPase alpha2-subunit causing familial hemiplegic migraine type 2 Recurrent coma and fever in familial hemiplegic migraine type 2. A prospective 15-year follow-up of a large family with a novel ATP1A2 mutation.Pain research update from a genetic point of view.Familial and sporadic hemiplegic migraine: diagnosis and treatment.A novel ATP1A2 gene mutation in an Irish familial hemiplegic migraine kindred.Glial overexpression of Dube3a causes seizures and synaptic impairments in Drosophila concomitant with down regulation of the Na+/K+ pump ATPα.Head tremor related to CACNA1A mutations.Hemiplegic migraine, seizures, progressive spastic paraparesis, mood disorder, and coma in siblings with low systemic serotonin.First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy.A new Italian FHM2 family: clinical aspects and functional analysis of the disease-associated mutation.Screen for CACNA1A and ATP1A2 Mutations in Sporadic Hemiplegic Migraine Patients Hemiplegic Migraine: Clinical Features, Links with Basilar-type Migraine, Current and Future Treatment Amino acid changes in the amino terminus of the Na,K-adenosine triphosphatase alpha-2 subunit associated to familial and sporadic hemiplegic migraine

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P2860

A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs

http://www.wikidata.org/entity/Q28285675

description

2004 nî lūn-bûn

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2004 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2004 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2004年の論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年论文

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name

A G301R Na+/K+ -ATPase mutatio ...... e type 2 with cerebellar signs

@ast

A G301R Na+/K+ -ATPase mutatio ...... e type 2 with cerebellar signs

@en

A G301R Na+/K+ -ATPase mutatio ...... e type 2 with cerebellar signs

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type

label

A G301R Na+/K+ -ATPase mutatio ...... e type 2 with cerebellar signs

@ast

A G301R Na+/K+ -ATPase mutatio ...... e type 2 with cerebellar signs

@en

A G301R Na+/K+ -ATPase mutatio ...... e type 2 with cerebellar signs

@nl

prefLabel

A G301R Na+/K+ -ATPase mutatio ...... e type 2 with cerebellar signs

@ast

A G301R Na+/K+ -ATPase mutatio ...... e type 2 with cerebellar signs

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A G301R Na+/K+ -ATPase mutatio ...... e type 2 with cerebellar signs

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A G301R Na+/K+ -ATPase mutatio ...... e type 2 with cerebellar signs

@en

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Antonini Giovanni

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

Frank Lehmann-Horn

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Giovanni Antonini

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Giunti Paola

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Maria Spadaro

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Marina Frontali

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Simona Ursu

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Veneziano Liana

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P2860

A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia

CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy

Decreased hemispheric water mobility in hemiplegic migraine related to mutation of CACNA1A gene.

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s10048-004-0183-2

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177-85

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10.1007/S10048-004-0183-2

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3

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5

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Liana Veneziano

Karin Jurkat-Rott

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2004-09-01T00:00:00Z

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8255397

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migraine disorder