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Items: 1 to 20 of 218

1.

De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine.

Riant F, Ducros A, Ploton C, Barbance C, Depienne C, Tournier-Lasserve E.

Neurology. 2010 Sep 14;75(11):967-72. doi: 10.1212/WNL.0b013e3181f25e8f.

PMID:
20837964
2.

Screen for CACNA1A and ATP1A2 mutations in sporadic hemiplegic migraine patients.

Thomsen LL, Oestergaard E, Bjornsson A, Stefansson H, Fasquel AC, Gulcher J, Stefansson K, Olesen J.

Cephalalgia. 2008 Sep;28(9):914-21. doi: 10.1111/j.1468-2982.2008.01599.x. Epub 2008 May 30.

PMID:
18513263
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.

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
5.

FHM3 in familial hemiplegic migraine is more resistant to mutation than FHM1 and FHM2.

Wiwanitkit V.

J Neurol Sci. 2009 Feb 15;277(1-2):76-9. doi: 10.1016/j.jns.2008.10.012. Epub 2008 Nov 13.

PMID:
19007941
6.

Management of sporadic and familial hemiplegic migraine.

Russell MB.

Expert Rev Neurother. 2010 Mar;10(3):381-7. doi: 10.1586/ern.09.127. Review.

PMID:
20187861
7.

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.

Eur J Hum Genet. 2006 May;14(5):555-60.

8.

Migrainous vertigo: mutation analysis of the candidate genes CACNA1A, ATP1A2, SCN1A, and CACNB4.

von Brevern M, Ta N, Shankar A, Wiste A, Siegel A, Radtke A, Sander T, Escayg A.

Headache. 2006 Jul-Aug;46(7):1136-41.

PMID:
16866717
9.

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
10.

A long-term follow-up study of 18 patients with sporadic hemiplegic migraine.

Stam AH, Louter MA, Haan J, de Vries B, van den Maagdenberg AM, Frants RR, Ferrari MD, Terwindt GM.

Cephalalgia. 2011 Jan;31(2):199-205. doi: 10.1177/0333102410375629. Epub 2010 Jul 2.

PMID:
20974584
11.

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
12.

Genetic heterogeneity in Italian families with familial hemiplegic migraine.

Carrera P, Piatti M, Stenirri S, Grimaldi LM, Marchioni E, Curcio M, Righetti PG, Ferrari M, Gelfi C.

Neurology. 1999 Jul 13;53(1):26-33.

PMID:
10408532
13.

Genetic analysis of 27 Spanish patients with hemiplegic migraine, basilar-type migraine and childhood periodic syndromes.

Cuenca-León E, Corominas R, Fernàndez-Castillo N, Volpini V, Del Toro M, Roig M, Macaya A, Cormand B.

Cephalalgia. 2008 Oct;28(10):1039-47. doi: 10.1111/j.1468-2982.2008.01645.x. Epub 2008 Jul 17.

PMID:
18644040
14.

Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine.

de Vries B, Freilinger T, Vanmolkot KR, Koenderink JB, Stam AH, Terwindt GM, Babini E, van den Boogerd EH, van den Heuvel JJ, Frants RR, Haan J, Pusch M, van den Maagdenberg AM, Ferrari MD, Dichgans M.

Neurology. 2007 Dec 4;69(23):2170-6.

PMID:
18056581
15.

Mutation analysis of CACNA1A and ATP1A2 genes in Brazilian FHM families.

Lopes LR, Peres MF, Vanmolkot KR, Tobo PR, Zukerman E, Frants RR, van den Maagdenberg AM, Moreira-Filho CA.

Arq Neuropsiquiatr. 2006 Sep;64(3A):549-52.

16.

Sporadic hemiplegic migraine in children.

Pienczk-Reclawowicz K, Pilarska E, Lemka M.

Neurol India. 2010 Jul-Aug;58(4):512-3. doi: 10.4103/0028-3886.68659. No abstract available.

17.

Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group.

Terwindt GM, Ophoff RA, Haan J, Vergouwe MN, van Eijk R, Frants RR, Ferrari MD.

Neurology. 1998 Apr;50(4):1105-10.

PMID:
9566402
18.

CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhood.

de Vries B, Stam AH, Beker F, van den Maagdenberg AM, Vanmolkot KR, Laan L, Ginjaar IB, Frants RR, Lauffer H, Haan J, Haas JP, Terwindt GM, Ferrari MD.

Cephalalgia. 2008 Aug;28(8):887-91. doi: 10.1111/j.1468-2982.2008.01596.x. Epub 2008 May 21.

PMID:
18498393
19.

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.

20.

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

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