PubMed (OMIM) for id: 355962

Year	Number of Results
1988	1
1992	1
1997	2
1999	3
2003	4
2004	6
2005	2
2023	0

1

Genomewide significant linkage to migrainous headache on chromosome 5q21.

Nyholt DR, Morley KI, Ferreira MA, Medland SE, Boomsma DI, Heath AC, Merikangas KR, Montgomery GW, Martin NG. Nyholt DR, et al. Am J Hum Genet. 2005 Sep;77(3):500-12. doi: 10.1086/444510. Epub 2005 Jul 28. Am J Hum Genet. 2005. PMID: 16080125 Free PMC article.

2

Opening of the blood-brain barrier preceding cortical edema in a severe attack of FHM type II.

Dreier JP, Jurkat-Rott K, Petzold GC, Tomkins O, Klingebiel R, Kopp UA, Lehmann-Horn F, Friedman A, Dichgans M. Dreier JP, et al. Neurology. 2005 Jun 28;64(12):2145-7. doi: 10.1212/01.WNL.0000176298.63840.99. Neurology. 2005. PMID: 15985592

3

A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs.

Spadaro M, Ursu S, Lehmann-Horn F, Veneziano L, Antonini G, Giunti P, Frontali M, Jurkat-Rott K. Spadaro M, et al. Neurogenetics. 2004 Sep;5(3):177-85. doi: 10.1007/s10048-004-0183-2. Epub 2004 Jul 31. Neurogenetics. 2004. PMID: 15459825

4

Kinetic alterations due to a missense mutation in the Na,K-ATPase alpha2 subunit cause familial hemiplegic migraine type 2.

Segall L, Scanzano R, Kaunisto MA, Wessman M, Palotie A, Gargus JJ, Blostein R. Segall L, et al. J Biol Chem. 2004 Oct 15;279(42):43692-6. doi: 10.1074/jbc.M407471200. Epub 2004 Aug 11. J Biol Chem. 2004. PMID: 15308625 Free article.

5

A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood.

Bassi MT, Bresolin N, Tonelli A, Nazos K, Crippa F, Baschirotto C, Zucca C, Bersano A, Dolcetta D, Boneschi FM, Barone V, Casari G. Bassi MT, et al. J Med Genet. 2004 Aug;41(8):621-8. doi: 10.1136/jmg.2003.017863. J Med Genet. 2004. PMID: 15286158 Free PMC article. No abstract available.

6

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. Swoboda KJ, et al. Ann Neurol. 2004 Jun;55(6):884-7. doi: 10.1002/ana.20134. Ann Neurol. 2004. PMID: 15174025

7

Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants.

Jurkat-Rott K, Freilinger T, Dreier JP, Herzog J, Göbel H, Petzold GC, Montagna P, Gasser T, Lehmann-Horn F, Dichgans M. Jurkat-Rott K, et al. Neurology. 2004 May 25;62(10):1857-61. doi: 10.1212/01.wnl.0000127310.11526.fd. Neurology. 2004. PMID: 15159495

8

A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2.

Kaunisto MA, Harno H, Vanmolkot KR, Gargus JJ, Sun G, Hämäläinen E, Liukkonen E, Kallela M, van den Maagdenberg AM, Frants RR, Färkkilä M, Palotie A, Wessman M. Kaunisto MA, et al. Neurogenetics. 2004 Jun;5(2):141-6. doi: 10.1007/s10048-004-0178-z. Epub 2004 May 7. Neurogenetics. 2004. PMID: 15133718

9

Alternating hemiplegia of childhood: a syndrome inherited with an autosomal dominant trait.

Kanavakis E, Xaidara A, Papathanasiou-Klontza D, Papadimitriou A, Velentza S, Youroukos S. Kanavakis E, et al. Dev Med Child Neurol. 2003 Dec;45(12):833-6. doi: 10.1017/s0012162203001543. Dev Med Child Neurol. 2003. PMID: 14667076 Free article.

10

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

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