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Results: 1 to 20 of 105

Similar articles for PubMed (Select 24928127)

1.

PRRT2 and hemiplegic migraine: a complex association.

Pelzer N, de Vries B, Kamphorst JT, Vijfhuizen LS, Ferrari MD, Haan J, van den Maagdenberg AM, Terwindt GM.

Neurology. 2014 Jul 15;83(3):288-90. doi: 10.1212/WNL.0000000000000590. Epub 2014 Jun 13. No abstract available.

PMID:
24928127
2.

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
3.

PRRT2 mutation causes paroxysmal kinesigenic dyskinesia and hemiplegic migraine in monozygotic twins.

Castiglioni C, López I, Riant F, Bertini E, Terracciano A.

Eur J Paediatr Neurol. 2013 May;17(3):254-8. doi: 10.1016/j.ejpn.2012.10.010. Epub 2012 Nov 19.

PMID:
23182655
4.

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.

PMID:
19874388
5.

Comment: challenges in defining the clinical spectrum of neurogenetic disorders.

Jen JC.

Neurology. 2014 Jul 15;83(3):290. doi: 10.1212/WNL.0000000000000603. Epub 2014 Jun 13. No abstract available.

PMID:
24928122
6.

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
7.

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.

Neurogenetics. 2004 Jun;5(2):141-6. Epub 2004 May 7.

PMID:
15133718
8.

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.

9.

A novel ATP1A2 gene mutation in familial hemiplegic migraine and epilepsy.

Costa C, Prontera P, Sarchielli P, Tonelli A, Bassi MT, Cupini LM, Caproni S, Siliquini S, Donti E, Calabresi P.

Cephalalgia. 2014 Jan;34(1):68-72. doi: 10.1177/0333102413498941. Epub 2013 Aug 5.

PMID:
23918834
10.

[ATP1A2: a key player in familial hemiplegic migraine].

Blostein R, Segall L, Gargus JJ.

Med Sci (Paris). 2006 Apr;22(4):341-3. French. No abstract available.

11.

PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine.

Cloarec R, Bruneau N, Rudolf G, Massacrier A, Salmi M, Bataillard M, Boulay C, Caraballo R, Fejerman N, Genton P, Hirsch E, Hunter A, Lesca G, Motte J, Roubertie A, Sanlaville D, Wong SW, Fu YH, Rochette J, Ptácek LJ, Szepetowski P.

Neurology. 2012 Nov 20;79(21):2097-103. doi: 10.1212/WNL.0b013e3182752c46. Epub 2012 Oct 17.

12.

Alterations in the alpha2 isoform of Na,K-ATPase associated with familial hemiplegic migraine type 2.

Segall L, Mezzetti A, Scanzano R, Gargus JJ, Purisima E, Blostein R.

Proc Natl Acad Sci U S A. 2005 Aug 2;102(31):11106-11. Epub 2005 Jul 21.

13.

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.

14.

Functional effects of Na+,K+-ATPase gene mutations linked to familial hemiplegic migraine.

Capendeguy O, Horisberger JD.

Neuromolecular Med. 2004;6(2-3):105-16.

PMID:
15970628
15.

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.

J Biol Chem. 2004 Oct 15;279(42):43692-6. Epub 2004 Aug 11.

16.

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
17.

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.

Neurology. 2004 May 25;62(10):1857-61.

PMID:
15159495
18.

PRRT2 mutations and paroxysmal disorders.

Méneret A, Gaudebout C, Riant F, Vidailhet M, Depienne C, Roze E.

Eur J Neurol. 2013 Jun;20(6):872-8. doi: 10.1111/ene.12104. Epub 2013 Feb 9. Review.

PMID:
23398397
19.

Familial PRRT2 mutation with heterogeneous paroxysmal disorders including paroxysmal torticollis and hemiplegic migraine.

Dale RC, Gardiner A, Antony J, Houlden H.

Dev Med Child Neurol. 2012 Oct;54(10):958-60. doi: 10.1111/j.1469-8749.2012.04394.x. Epub 2012 Jul 31.

PMID:
22845787
20.

Episodic movement disorders: from phenotype to genotype and back.

Brockmann K.

Curr Neurol Neurosci Rep. 2013 Oct;13(10):379. doi: 10.1007/s11910-013-0379-7. Review.

PMID:
23963607
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