Similar articles for PMID: 12953268

Year	Number of Results
1874	1
1965	1
1981	1
1983	1
1993	1
1994	4
1996	6
1997	4
1998	3
1999	6
2000	6
2001	15
2002	12
2003	12
2004	21
2005	18
2006	19
2007	18
2008	28
2009	15
2010	17
2011	16
2012	21
2013	22
2014	17
2015	6
2016	10
2017	12
2018	14
2019	9
2020	13
2021	10
2022	7
2023	2
2024	1

1

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. Vanmolkot KR, et al. Ann Neurol. 2003 Sep;54(3):360-6. doi: 10.1002/ana.10674. Ann Neurol. 2003. PMID: 12953268

2

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. Thomsen LL, et al. Brain. 2007 Feb;130(Pt 2):346-56. doi: 10.1093/brain/awl334. Epub 2006 Dec 2. Brain. 2007. PMID: 17142831

3

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. Vanmolkot KR, et al. Eur J Hum Genet. 2007 Aug;15(8):884-8. doi: 10.1038/sj.ejhg.5201841. Epub 2007 May 2. Eur J Hum Genet. 2007. PMID: 17473835

4

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

Fernandez DM, Hand CK, Sweeney BJ, Parfrey NA. Fernandez DM, et al. Headache. 2008 Jan;48(1):101-8. doi: 10.1111/j.1526-4610.2007.00848.x. Headache. 2008. PMID: 18184292

5

Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine.

Vanmolkot KR, Kors EE, Turk U, Turkdogan D, Keyser A, Broos LA, Kia SK, van den Heuvel JJ, Black DF, Haan J, Frants RR, Barone V, Ferrari MD, Casari G, Koenderink JB, van den Maagdenberg AM. Vanmolkot KR, et al. Eur J Hum Genet. 2006 May;14(5):555-60. doi: 10.1038/sj.ejhg.5201607. Eur J Hum Genet. 2006. PMID: 16538223

6

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. Pierelli F, et al. Cephalalgia. 2006 Mar;26(3):324-8. doi: 10.1111/j.1468-2982.2006.01002.x. Cephalalgia. 2006. PMID: 16472340

7

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. Tonelli A, et al. Clin Genet. 2007 Dec;72(6):517-23. doi: 10.1111/j.1399-0004.2007.00892.x. Epub 2007 Sep 18. Clin Genet. 2007. PMID: 17877748

8

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. Riant F, et al. Hum Mutat. 2005 Sep;26(3):281. doi: 10.1002/humu.9361. Hum Mutat. 2005. PMID: 16088919

9

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. Kors EE, et al. Neuropediatrics. 2004 Oct;35(5):293-6. doi: 10.1055/s-2004-821082. Neuropediatrics. 2004. PMID: 15534763

10

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

Spacey SD, Vanmolkot KR, Murphy C, van den Maagdenberg AM, Hsiung RG. Spacey SD, et al. Headache. 2005 Oct;45(9):1244-9. doi: 10.1111/j.1526-4610.2005.00249.x. Headache. 2005. PMID: 16178956

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