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Results: 1 to 20 of 89

1.

Pulmonary arterial hypertension in familial hemiplegic migraine with ATP1A2 channelopathy.

Montani D, Girerd B, Günther S, Riant F, Tournier-Lasserve E, Magy L, Maazi N, Guignabert C, Savale L, Sitbon O, Simonneau G, Soubrier F, Humbert M.

Eur Respir J. 2014 Feb;43(2):641-3. doi: 10.1183/09031936.00147013. Epub 2013 Oct 17. No abstract available.

PMID:
24136331
[PubMed - in process]
2.

Two novel functional mutations in the Na+,K+-ATPase alpha2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes.

Castro MJ, Nunes B, de Vries B, Lemos C, Vanmolkot KR, van den Heuvel JJ, Temudo T, Barros J, Sequeiros J, Frants RR, Koenderink JB, Pereira-Monteiro JM, van den Maagdenberg AM.

Clin Genet. 2008 Jan;73(1):37-43. Epub 2007 Nov 19.

PMID:
18028456
[PubMed - indexed for MEDLINE]
3.

A case of familial hemiplegic migraine associated with a novel ATP1A2 gene mutation.

De Cunto A, Bensa M, Tonelli A.

Pediatr Neurol. 2012 Aug;47(2):133-6. doi: 10.1016/j.pediatrneurol.2012.04.012.

PMID:
22759692
[PubMed - indexed for MEDLINE]
4.

Sporadic Hemiplegic Migraine with ATP1A2 and Prothrombin Gene Mutations.

Aceves J, Mungall D, Kirmani BF.

Case Rep Neurol Med. 2013;2013:895057. doi: 10.1155/2013/895057. Epub 2013 Dec 11.

PMID:
24396618
[PubMed]
Free PMC Article
5.

Acute encephalopathy in familial hemiplegic migraine with ATP1A2 mutation.

Merwick A, Fernandez D, McNamara B, Harrington H.

BMJ Case Rep. 2013 Jun 10;2013. pii: bcr2013009750. doi: 10.1136/bcr-2013-009750.

PMID:
23761507
[PubMed - in process]
6.

Genetic effects of ATP1A2 in familial hemiplegic migraine type II and animal models.

Gritz SM, Radcliffe RA.

Hum Genomics. 2013 Apr 5;7:8. doi: 10.1186/1479-7364-7-8. Review.

PMID:
23561701
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

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

Dichgans M, Freilinger T, Eckstein G, Babini E, Lorenz-Depiereux B, Biskup S, Ferrari MD, Herzog J, van den Maagdenberg AM, Pusch M, Strom TM.

Lancet. 2005 Jul 30-Aug 5;366(9483):371-7.

PMID:
16054936
[PubMed - indexed for MEDLINE]
8.

The genetic features of 24 patients affected by familial and sporadic hemiplegic migraine.

Gallanti A, Cardin V, Tonelli A, Bussone G, Bresolin N, Mariani C, Bassi MT.

Neurol Sci. 2011 May;32 Suppl 1:S141-2. doi: 10.1007/s10072-011-0517-4.

PMID:
21533730
[PubMed - indexed for MEDLINE]
9.

Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: clinical, genetic, and functional studies.

Carreño O, Corominas R, Serra SA, Sintas C, Fernández-Castillo N, Vila-Pueyo M, Toma C, Gené GG, Pons R, Llaneza M, Sobrido MJ, Grinberg D, Valverde MÁ, Fernández-Fernández JM, Macaya A, Cormand B.

Mol Genet Genomic Med. 2013 Nov;1(4):206-22. doi: 10.1002/mgg3.24. Epub 2013 Jul 2.

PMID:
24498617
[PubMed]
Free PMC Article
10.

First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraine.

Vanmolkot KR, Stam AH, Raman A, Koenderink JB, de Vries B, van den Boogerd EH, van Vark J, van den Heuvel JJ, Bajaj N, Terwindt GM, Haan J, Frants RR, Ferrari MD, van den Maagdenberg AM.

Eur J Hum Genet. 2007 Aug;15(8):884-8. Epub 2007 May 2.

PMID:
17473835
[PubMed - indexed for MEDLINE]
Free Article
11.

Transient nonverbal learning disorder in a child suffering from Familial Hemiplegic Migraine.

Podestà B, Briatore E, Boghi A, Marenco D, Calzolari S.

Cephalalgia. 2011 Oct;31(14):1497-502. doi: 10.1177/0333102411418260. Epub 2011 Sep 9.

PMID:
21908445
[PubMed - indexed for MEDLINE]
12.

A novel ATP1A2 gene mutation in an Irish familial hemiplegic migraine kindred.

Fernandez DM, Hand CK, Sweeney BJ, Parfrey NA.

Headache. 2008 Jan;48(1):101-8. doi: 10.1111/j.1526-4610.2007.00848.x.

PMID:
18184292
[PubMed - indexed for MEDLINE]
13.

A novel de novo nonsense mutation in ATP1A2 associated with sporadic hemiplegic migraine and epileptic seizures.

Gallanti A, Tonelli A, Cardin V, Bussone G, Bresolin N, Bassi MT.

J Neurol Sci. 2008 Oct 15;273(1-2):123-6. doi: 10.1016/j.jns.2008.06.006. Epub 2008 Jul 21.

PMID:
18644608
[PubMed - indexed for MEDLINE]
14.

A wide clinical phenotype spectrum in patients with ATP1A2 mutations.

Al-Bulushi B, Al-Hashem A, Tabarki B.

J Child Neurol. 2014 Feb;29(2):265-8. doi: 10.1177/0883073813504623. Epub 2013 Oct 4.

PMID:
24097848
[PubMed - in process]
15.

Alternating hemiplegia of childhood: no mutations in the second familial hemiplegic migraine gene ATP1A2.

Kors EE, Vanmolkot KR, Haan J, Kheradmand Kia S, Stroink H, Laan LA, Gill DS, Pascual J, van den Maagdenberg AM, Frants RR, Ferrari MD.

Neuropediatrics. 2004 Oct;35(5):293-6.

PMID:
15534763
[PubMed - indexed for MEDLINE]
16.

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

De Fusco M, Marconi R, Silvestri L, Atorino L, Rampoldi L, Morgante L, Ballabio A, Aridon P, Casari G.

Nat Genet. 2003 Feb;33(2):192-6. Epub 2003 Jan 21.

PMID:
12539047
[PubMed - indexed for MEDLINE]
17.

Impaired plasma membrane targeting or protein stability by certain ATP1A2 mutations identified in sporadic or familial hemiplegic migraine.

Tavraz NN, Dürr KL, Koenderink JB, Freilinger T, Bamberg E, Dichgans M, Friedrich T.

Channels (Austin). 2009 Mar-Apr;3(2):82-7. Epub 2009 Mar 3.

PMID:
19372756
[PubMed - indexed for MEDLINE]
Free Article
18.

Prolonged sporadic hemiplegic migraine associated with a novel de novo missense ATP1A2 gene mutation.

De Sanctis S, Grieco GS, Breda L, Casali C, Nozzi M, Del Torto M, Chiarelli F, Verrotti A.

Headache. 2011 Mar;51(3):447-50. doi: 10.1111/j.1526-4610.2010.01793.x. Epub 2010 Nov 4.

PMID:
21352219
[PubMed - indexed for MEDLINE]
19.

ATP1A2 mutations in 11 families with familial hemiplegic migraine.

Riant F, De Fusco M, Aridon P, Ducros A, Ploton C, Marchelli F, Maciazek J, Bousser MG, Casari G, Tournier-Lasserve E.

Hum Mutat. 2005 Sep;26(3):281.

PMID:
16088919
[PubMed - indexed for MEDLINE]
20.

Genetics of migraine: an update with special attention to genetic comorbidity.

Stam AH, van den Maagdenberg AM, Haan J, Terwindt GM, Ferrari MD.

Curr Opin Neurol. 2008 Jun;21(3):288-93. doi: 10.1097/WCO.0b013e3282fd171a. Review.

PMID:
18451712
[PubMed - indexed for MEDLINE]

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