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Items: 1 to 20 of 324

1.

Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation.

Swoboda KJ, Kanavakis E, Xaidara A, Johnson JE, Leppert MF, Schlesinger-Massart MB, Ptacek LJ, Silver K, Youroukos S.

Ann Neurol. 2004 Jun;55(6):884-7.

PMID:
15174025
2.

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
3.

The genetic spectrum of a population-based sample of familial hemiplegic migraine.

Thomsen LL, Kirchmann M, Bjornsson A, Stefansson H, Jensen RM, Fasquel AC, Petursson H, Stefansson M, Frigge ML, Kong A, Gulcher J, Stefansson K, Olesen J.

Brain. 2007 Feb;130(Pt 2):346-56. Epub 2006 Dec 2.

PMID:
17142831
4.

Epilepsy as part of the phenotype associated with ATP1A2 mutations.

Deprez L, Weckhuysen S, Peeters K, Deconinck T, Claeys KG, Claes LR, Suls A, Van Dyck T, Palmini A, Matthijs G, Van Paesschen W, De Jonghe P.

Epilepsia. 2008 Mar;49(3):500-8. Epub 2007 Nov 19.

5.

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

Vanmolkot KR, Kors EE, Hottenga JJ, Terwindt GM, Haan J, Hoefnagels WA, Black DF, Sandkuijl LA, Frants RR, Ferrari MD, van den Maagdenberg AM.

Ann Neurol. 2003 Sep;54(3):360-6.

PMID:
12953268
6.

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
7.

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
8.

Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutation.

de Vries B, Stam AH, Kirkpatrick M, Vanmolkot KR, Koenderink JB, van den Heuvel JJ, Stunnenberg B, Goudie D, Shetty J, Jain V, van Vark J, Terwindt GM, Frants RR, Haan J, van den Maagdenberg AM, Ferrari MD.

Epilepsia. 2009 Nov;50(11):2503-4. doi: 10.1111/j.1528-1167.2009.02186.x. No abstract available.

9.

Familial basilar migraine associated with a new mutation in the ATP1A2 gene.

Ambrosini A, D'Onofrio M, Grieco GS, Di Mambro A, Montagna G, Fortini D, Nicoletti F, Nappi G, Sances G, Schoenen J, Buzzi MG, Santorelli FM, Pierelli F.

Neurology. 2005 Dec 13;65(11):1826-8.

PMID:
16344534
10.

Alternating hemiplegia of childhood: no mutations in the glutamate transporter EAAT1.

de Vries B, Haan J, Stam AH, Vanmolkot KR, Stroink H, Laan LA, Gill DS, Pascual J, Frants RR, van den Maagdenberg AM, Ferrari MD.

Neuropediatrics. 2006 Oct;37(5):302-4.

PMID:
17236110
11.

Familial hemiplegic migraine presenting as recurrent encephalopathy in a Native Indian family.

Spacey SD, Vanmolkot KR, Murphy C, van den Maagdenberg AM, Hsiung RG.

Headache. 2005 Oct;45(9):1244-9.

PMID:
16178956
12.

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
13.

Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine.

Castro MJ, Stam AH, Lemos C, Barros J, Gouveia RG, Martins IP, Koenderink JB, Vanmolkot KR, Mendes AP, Frants RR, Ferrari MD, Sequeiros J, Pereira-Monteiro JM, van den Maagdenberg AM.

J Hum Genet. 2007;52(12):990-8. Epub 2007 Oct 19.

PMID:
17952365
14.

Severe attacks of familial hemiplegic migraine, childhood epilepsy and ATP1A2 mutation.

Lebas A, Guyant-Maréchal L, Hannequin D, Riant F, Tournier-Lasserve E, Parain D.

Cephalalgia. 2008 Jul;28(7):774-7. doi: 10.1111/j.1468-2982.2008.01603.x. Epub 2008 May 21.

PMID:
18498390
15.

A novel ATP1A2 mutation in a family with FHM type II.

Pierelli F, Grieco GS, Pauri F, Pirro C, Fiermonte G, Ambrosini A, Costa A, Buzzi MG, Valoppi M, Caltagirone C, Nappi G, Santorelli FM.

Cephalalgia. 2006 Mar;26(3):324-8.

PMID:
16472340
16.

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
17.

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
18.

Amino acid changes in the amino terminus of the Na,K-adenosine triphosphatase alpha-2 subunit associated to familial and sporadic hemiplegic migraine.

Tonelli A, Gallanti A, Bersano A, Cardin V, Ballabio E, Airoldi G, Redaelli F, Candelise L, Bresolin N, Bassi MT.

Clin Genet. 2007 Dec;72(6):517-23. Epub 2007 Sep 18.

PMID:
17877748
19.

The CACNA1A and ATP1A2 genes are not involved in dominantly inherited migraine with aura.

Kirchmann M, Thomsen LL, Olesen J.

Am J Med Genet B Neuropsychiatr Genet. 2006 Apr 5;141B(3):250-6.

PMID:
16508934
20.

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.

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