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Items: 12

1.

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.

2.

Sporadic hemiplegic migraine with permanent neurological deficits.

Schwedt TJ, Zhou J, Dodick DW.

Headache. 2014 Jan;54(1):163-6. doi: 10.1111/head.12232. Epub 2013 Oct 10.

3.

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.

4.

The primary headaches: genetics, epigenetics and a behavioural genetic model.

Montagna P.

J Headache Pain. 2008 Apr;9(2):57-69. doi: 10.1007/s10194-008-0026-x. Epub 2008 Mar 15.

5.

Association analysis of chromosome 1 migraine candidate genes.

Fernandez F, Curtain RP, Colson NJ, Ovcaric M, MacMillan J, Griffiths LR.

BMC Med Genet. 2007 Aug 29;8:57.

6.

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.

Am J Hum Genet. 2005 Sep;77(3):500-12. Epub 2005 Jul 28.

7.

A new susceptibility locus for migraine with aura in the 15q11-q13 genomic region containing three GABA-A receptor genes.

Russo L, Mariotti P, Sangiorgi E, Giordano T, Ricci I, Lupi F, Chiera R, Guzzetta F, Neri G, Gurrieri F.

Am J Hum Genet. 2005 Feb;76(2):327-33. Epub 2004 Dec 7.

8.

Localization of a gene for migraine without aura to chromosome 4q21.

Björnsson A, Gudmundsson G, Gudfinnsson E, Hrafnsdóttir M, Benedikz J, Skúladóttir S, Kristjánsson K, Frigge ML, Kong A, Stefánsson K, Gulcher JR.

Am J Hum Genet. 2003 Nov;73(5):986-93. Epub 2003 Sep 25. Erratum in: Am J Hum Genet. 2005 Apr;76(4):715.

9.

A locus for migraine without aura maps on chromosome 14q21.2-q22.3.

Soragna D, Vettori A, Carraro G, Marchioni E, Vazza G, Bellini S, Tupler R, Savoldi F, Mostacciuolo ML.

Am J Hum Genet. 2003 Jan;72(1):161-7. Epub 2002 Dec 9.

10.

A susceptibility locus for migraine with aura, on chromosome 4q24.

Wessman M, Kallela M, Kaunisto MA, Marttila P, Sobel E, Hartiala J, Oswell G, Leal SM, Papp JC, Hämäläinen E, Broas P, Joslyn G, Hovatta I, Hiekkalinna T, Kaprio J, Ott J, Cantor RM, Zwart JA, Ilmavirta M, Havanka H, Färkkilä M, Peltonen L, Palotie A.

Am J Hum Genet. 2002 Mar;70(3):652-62. Epub 2002 Feb 8.

11.

The inheritance of migraine with aura estimated by means of structural equation modelling.

Ulrich V, Gervil M, Kyvik KO, Olesen J, Russell MB.

J Med Genet. 1999 Mar;36(3):225-7.

12.

Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia.

Ducros A, Denier C, Joutel A, Vahedi K, Michel A, Darcel F, Madigand M, Guerouaou D, Tison F, Julien J, Hirsch E, Chedru F, Bisgård C, Lucotte G, Després P, Billard C, Barthez MA, Ponsot G, Bousser MG, Tournier-Lasserve E.

Am J Hum Genet. 1999 Jan;64(1):89-98.

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