Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions
about
sameAs
Association analysis of chromosome 1 migraine candidate genesAlterations in the alpha2 isoform of Na,K-ATPase associated with familial hemiplegic migraine type 2De novo mutations in ATP1A3 cause alternating hemiplegia of childhoodThe cerebellum and migraineATP1A2 Mutations in Migraine: Seeing through the Facets of an Ion Pump onto the Neurobiology of DiseaseGenetic epilepsy syndromes without structural brain abnormalities: clinical features and experimental modelsIctal epileptic headache: an old story with courses and appealsMigraine headache: a review of the molecular genetics of a common disorderNovel role of ouabain as a cystogenic factor in autosomal dominant polycystic kidney diseaseThe phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 geneA novel ATP1A2 mutation in a family with FHM type IITwo de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migrainePainful heat reveals hyperexcitability of the temporal pole in interictal and ictal migraine StatesIncreased susceptibility to cortical spreading depression in the mouse model of familial hemiplegic migraine type 2.Migraine: new molecular mechanisms.Familial hemiplegic migraine.The genetic relationship between epilepsy and hemiplegic migrainePotassium dynamics in the epileptic cortex: new insights on an old topic.Genetic testing in the epilepsies--report of the ILAE Genetics CommissionGenomewide significant linkage to migrainous headache on chromosome 5q21.Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?High prevalence of headaches in patients with epilepsy.Identification of ATP1A3 mutations by exome sequencing as the cause of alternating hemiplegia of childhood in Japanese patients.Neuropathology in Drosophila membrane excitability mutantsMigraine and epilepsy: genetically linked?Overview of diagnosis and management of paediatric headache. Part I: diagnosisMigraine genetics.Ictal headache and visual sensitivity.Polymorphisms of the SCN1A gene in children and adolescents with primary headache and idiopathic or cryptogenic epilepsy: is there a linkage?Ouabain binding site in a functioning Na+/K+ ATPaseThe molecular genetics of migraine.Migraine pathophysiology.Prolonged hemiplegic episodes in children due to mutations in ATP1A2.Headaches add to the burden of epilepsy.Intravenous nimodipine worsening prolonged attack of familial hemiplegic migraine.Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3Headache, epilepsy and photosensitivity: how are they connected?Neonatal epilepsy syndromes and generalized epilepsy with febrile seizures plus (GEFS+).FXYD proteins: new regulators of Na-K-ATPase.PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine
P2860
Q21261440-A846D96F-1843-4E70-B5A8-0B98E11CC665Q24531852-98448A38-F483-41C4-8E14-5D286421D1F1Q24600468-7347350F-1AE5-4835-B230-09A9FFE99A84Q24628942-448A9AE1-C679-4506-8AE2-72F7DA79BCFAQ26738318-22D43385-0343-4521-AA34-588FB81041DFQ26861471-9471FA81-0C34-4163-A2B4-7396E18D9AE8Q27001097-055D3CFF-296D-43DA-A359-9C6F54A08752Q27010458-A7355B52-3778-4C76-81D0-5707A8869BD9Q27011660-B443ED09-8712-43AF-9EB6-87BE132F4183Q28286980-3FDBA243-CC73-4DE0-AABD-8730EEDD2FBDQ28296728-C1710336-0012-4387-B99A-365BD5ACA2F3Q28302086-D280CDD8-8FFB-408A-9C16-5FE886C1C9D3Q30497886-F42B1AAA-D934-43E9-BA5A-6CFD59DE30DEQ31022226-41CF4C20-CA9C-41EE-8160-B637C6640E07Q33220839-886C4897-F5BB-4741-BF95-3EE43CEB64FDQ33280531-05189E9E-1AB3-47A3-8876-E3E7F7878301Q33621149-4F687B59-0F78-4CF3-9196-98DE4124C331Q33788071-10DFC431-3569-4F31-8117-AA5C4F55821FQ33794130-BD2FF0B5-AF06-4826-B708-320A9F2C34EFQ34021170-C675E5F9-6B3B-4673-889E-0D94C1A9FCC5Q34249436-986BCBDA-E8A6-4EC9-8570-4C8B02705F49Q34506938-79E0F2F2-5810-4EF8-923B-05A493B736C6Q34586667-AFEB4697-F6AC-4D9A-AAF3-BB60D481A897Q34587578-E93341D8-B3D1-42A9-81C3-0FC131E663FFQ34657045-D020205E-4841-4777-AAB0-4A08340D3119Q34663702-F1A3CBA4-09CE-45A5-87B7-95426B5B3BB5Q34817871-85C88968-2946-48DC-9B45-3C26AE6C9499Q34839837-5FD8F824-5FCD-4D6F-AB3C-E386D0A65BEAQ35113513-D5219260-832A-4A59-8BBB-04F5BE79429AQ35516161-E3BDF3A3-9076-4DA9-9F7D-02BCEB2A34B1Q35932365-97C9F68C-8676-4172-BCA6-18537083B4C8Q36099504-DF194B47-D8CB-4D3B-B004-8E706261E597Q36227369-103A3B42-F122-4F5C-9783-DFB65F6CA3BAQ36259612-FE74C073-9D33-4B75-A315-3013DBB8891EQ36260611-826FDB97-4ABB-4270-B5C1-C55DDA4E8C37Q36295287-8F9A40F4-8590-49A6-839E-E5798F8DE291Q36332667-AE8990C5-2A7F-498A-9786-059112369E30Q36344246-97A36923-3265-4855-B3A8-21EB74241AF8Q36364961-B9C8783B-C43A-41E1-9332-C37AEBD59C96Q36439205-B083B6C5-F6F2-47D3-9DED-96ACD6F2679E
P2860
Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions
description
2003 nî lūn-bûn
@nan
2003 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Novel mutations in the Na+, K+ ...... familial infantile convulsions
@ast
Novel mutations in the Na+, K+ ...... familial infantile convulsions
@en
Novel mutations in the Na+, K+ ...... familial infantile convulsions
@nl
type
label
Novel mutations in the Na+, K+ ...... familial infantile convulsions
@ast
Novel mutations in the Na+, K+ ...... familial infantile convulsions
@en
Novel mutations in the Na+, K+ ...... familial infantile convulsions
@nl
prefLabel
Novel mutations in the Na+, K+ ...... familial infantile convulsions
@ast
Novel mutations in the Na+, K+ ...... familial infantile convulsions
@en
Novel mutations in the Na+, K+ ...... familial infantile convulsions
@nl
P2093
P50
P3181
P356
P1433
P1476
Novel mutations in the Na+, K+ ...... familial infantile convulsions
@en
P2093
David F Black
Esther E Kors
Joost Haan
Kaate R J Vanmolkot
Lodewijk A Sandkuijl
Rune R Frants
Wil A J Hoefnagels
P3181
P356
10.1002/ANA.10674
P407
P577
2003-09-01T00:00:00Z