Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine
about
ATP1A2 Mutations in Migraine: Seeing through the Facets of an Ion Pump onto the Neurobiology of DiseaseThe Revolution in Migraine Genetics: From Aching Channels Disorders to a Next-Generation MedicineA homolog of FHM2 is involved in modulation of excitatory neurotransmission by serotonin in C. elegansFamilial hemiplegic migraine.The neurobiology of migraine.Cortical spreading depression-new insights and persistent questions.Prolonged hemiplegic episodes in children due to mutations in ATP1A2.Intravenous nimodipine worsening prolonged attack of familial hemiplegic migraine.Biomarkers in migraine: their promise, problems, and practical applications.Neuro-ophthalmologic manifestations of primary headache disorders.The structure of the Na+,K+-ATPase and mapping of isoform differences and disease-related mutations.Novel mutations affecting the Na, K ATPase alpha model complex neurological diseases and implicate the sodium pump in increased longevity.Migraine is a neuronal disease.Genetic effects of ATP1A2 in familial hemiplegic migraine type II and animal models.Ouabain attenuates the oxidative stress induced by lipopolysaccharides in the cerebellum of rats.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 2Inhibition of phosphorylation of na+,k+-ATPase by mutations causing familial hemiplegic migraine.Sporadic Hemiplegic Migraine with ATP1A2 and Prothrombin Gene Mutations.A novel ATP1A2 gene mutation in an Irish familial hemiplegic migraine kindred.Effects of Glia in a Triphasic Continuum Model of Cortical Spreading Depression.Pathophysiology of Migraine.Familial Hemiplegic Migraine Type 1 Shows no Hypersensitivity to Nitric OxideHemiplegic Migraine: Clinical Features, Links with Basilar-type Migraine, Current and Future TreatmentAmino acid changes in the amino terminus of the Na,K-adenosine triphosphatase alpha-2 subunit associated to familial and sporadic hemiplegic migraineDrosophila CaV2 channels harboring human migraine mutations cause synapse hyperexcitability that can be suppressed by inhibition of a Ca2+ store release pathway
P2860
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P2860
Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine
description
2006 nî lūn-bûn
@nan
2006 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Two de novo mutations in the N ...... e familial hemiplegic migraine
@ast
Two de novo mutations in the N ...... e familial hemiplegic migraine
@en
Two de novo mutations in the N ...... e familial hemiplegic migraine
@nl
type
label
Two de novo mutations in the N ...... e familial hemiplegic migraine
@ast
Two de novo mutations in the N ...... e familial hemiplegic migraine
@en
Two de novo mutations in the N ...... e familial hemiplegic migraine
@nl
prefLabel
Two de novo mutations in the N ...... e familial hemiplegic migraine
@ast
Two de novo mutations in the N ...... e familial hemiplegic migraine
@en
Two de novo mutations in the N ...... e familial hemiplegic migraine
@nl
P2093
P2860
P50
P3181
P356
P1476
Two de novo mutations in the N ...... e familial hemiplegic migraine
@en
P2093
Antoine Keyser
David F Black
Dylsad Turkdogan
Esther E Kors
Jan B Koenderink
Jeroen J M W van den Heuvel
Joost Haan
Kaate R J Vanmolkot
Ludo A M Broos
Rune R Frants
P2860
P2888
P304
P3181
P356
10.1038/SJ.EJHG.5201607
P407
P577
2006-05-01T00:00:00Z