226 related articles for article (PubMed ID: 18621678)
1. Divergent sodium channel defects in familial hemiplegic migraine.
Kahlig KM; Rhodes TH; Pusch M; Freilinger T; Pereira-Monteiro JM; Ferrari MD; van den Maagdenberg AM; Dichgans M; George AL
Proc Natl Acad Sci U S A; 2008 Jul; 105(28):9799-804. PubMed ID: 18621678
[TBL] [Abstract][Full Text] [Related]
2. Late sodium current blocker GS967 inhibits persistent currents induced by familial hemiplegic migraine type 3 mutations of the SCN1A gene.
Barbieri R; Bertelli S; Pusch M; Gavazzo P
J Headache Pain; 2019 Nov; 20(1):107. PubMed ID: 31730442
[TBL] [Abstract][Full Text] [Related]
3. Ranolazine selectively blocks persistent current evoked by epilepsy-associated Naν1.1 mutations.
Kahlig KM; Lepist I; Leung K; Rajamani S; George AL
Br J Pharmacol; 2010 Nov; 161(6):1414-26. PubMed ID: 20735403
[TBL] [Abstract][Full Text] [Related]
4. Self-limited hyperexcitability: functional effect of a familial hemiplegic migraine mutation of the Nav1.1 (SCN1A) Na+ channel.
Cestèle S; Scalmani P; Rusconi R; Terragni B; Franceschetti S; Mantegazza M
J Neurosci; 2008 Jul; 28(29):7273-83. PubMed ID: 18632931
[TBL] [Abstract][Full Text] [Related]
5. Early-onset familial hemiplegic migraine due to a novel SCN1A mutation.
Fan C; Wolking S; Lehmann-Horn F; Hedrich UB; Freilinger T; Lerche H; Borck G; Kubisch C; Jurkat-Rott K
Cephalalgia; 2016 Nov; 36(13):1238-1247. PubMed ID: 26763045
[TBL] [Abstract][Full Text] [Related]
6. First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy.
Castro MJ; Stam AH; Lemos C; de Vries B; Vanmolkot KR; Barros J; Terwindt GM; Frants RR; Sequeiros J; Ferrari MD; Pereira-Monteiro JM; van den Maagdenberg AM
Cephalalgia; 2009 Mar; 29(3):308-13. PubMed ID: 19220312
[TBL] [Abstract][Full Text] [Related]
7. Familial hemiplegic migraine due to L263V SCN1A mutation: discordance for epilepsy between two kindreds from Douro Valley.
Barros J; Ferreira A; Brandão AF; Lemos C; Correia F; Damásio J; Tuna A; Sequeiros J; Coutinho P; Alonso I; Pereira-Monteiro J
Cephalalgia; 2014 Oct; 34(12):1015-20. PubMed ID: 24646837
[TBL] [Abstract][Full Text] [Related]
8. Gain of function of sporadic/familial hemiplegic migraine-causing SCN1A mutations: Use of an optimized cDNA.
Bertelli S; Barbieri R; Pusch M; Gavazzo P
Cephalalgia; 2019 Apr; 39(4):477-488. PubMed ID: 29986598
[TBL] [Abstract][Full Text] [Related]
9. The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online.
Vanmolkot KR; Babini E; de Vries B; Stam AH; Freilinger T; Terwindt GM; Norris L; Haan J; Frants RR; Ramadan NM; Ferrari MD; Pusch M; van den Maagdenberg AM; Dichgans M
Hum Mutat; 2007 May; 28(5):522. PubMed ID: 17397047
[TBL] [Abstract][Full Text] [Related]
10. Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine.
Dichgans M; Freilinger T; Eckstein G; Babini E; Lorenz-Depiereux B; Biskup S; Ferrari MD; Herzog J; van den Maagdenberg AM; Pusch M; Strom TM
Lancet; 2005 Jul 30-Aug 5; 366(9483):371-7. PubMed ID: 16054936
[TBL] [Abstract][Full Text] [Related]
11. Sodium channel dysfunction in intractable childhood epilepsy with generalized tonic-clonic seizures.
Rhodes TH; Vanoye CG; Ohmori I; Ogiwara I; Yamakawa K; George AL
J Physiol; 2005 Dec; 569(Pt 2):433-45. PubMed ID: 16210358
[TBL] [Abstract][Full Text] [Related]
12. Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3.
Gargus JJ; Tournay A
Pediatr Neurol; 2007 Dec; 37(6):407-10. PubMed ID: 18021921
[TBL] [Abstract][Full Text] [Related]
13. A sodium channel mutation causing epilepsy in man exhibits subtle defects in fast inactivation and activation in vitro.
Alekov A; Rahman MM; Mitrovic N; Lehmann-Horn F; Lerche H
J Physiol; 2000 Dec; 529 Pt 3(Pt 3):533-9. PubMed ID: 11118488
[TBL] [Abstract][Full Text] [Related]
14. Nonfunctional NaV1.1 familial hemiplegic migraine mutant transformed into gain of function by partial rescue of folding defects.
Cestèle S; Schiavon E; Rusconi R; Franceschetti S; Mantegazza M
Proc Natl Acad Sci U S A; 2013 Oct; 110(43):17546-51. PubMed ID: 24101488
[TBL] [Abstract][Full Text] [Related]
15. Divergent effects of the T1174S SCN1A mutation associated with seizures and hemiplegic migraine.
Cestèle S; Labate A; Rusconi R; Tarantino P; Mumoli L; Franceschetti S; Annesi G; Mantegazza M; Gambardella A
Epilepsia; 2013 May; 54(5):927-35. PubMed ID: 23398611
[TBL] [Abstract][Full Text] [Related]
16. Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations.
Vahedi K; Depienne C; Le Fort D; Riant F; Chaine P; Trouillard O; Gaudric A; Morris MA; Leguern E; Tournier-Lasserve E; Bousser MG
Neurology; 2009 Mar; 72(13):1178-83. PubMed ID: 19332696
[TBL] [Abstract][Full Text] [Related]
17. Genetics of migraine: an update with special attention to genetic comorbidity.
Stam AH; van den Maagdenberg AM; Haan J; Terwindt GM; Ferrari MD
Curr Opin Neurol; 2008 Jun; 21(3):288-93. PubMed ID: 18451712
[TBL] [Abstract][Full Text] [Related]
18. Nonfunctional SCN1A is common in severe myoclonic epilepsy of infancy.
Ohmori I; Kahlig KM; Rhodes TH; Wang DW; George AL
Epilepsia; 2006 Oct; 47(10):1636-42. PubMed ID: 17054685
[TBL] [Abstract][Full Text] [Related]
19. Nav 1.1 dysfunction in genetic epilepsy with febrile seizures-plus or Dravet syndrome.
Volkers L; Kahlig KM; Verbeek NE; Das JH; van Kempen MJ; Stroink H; Augustijn P; van Nieuwenhuizen O; Lindhout D; George AL; Koeleman BP; Rook MB
Eur J Neurosci; 2011 Oct; 34(8):1268-75. PubMed ID: 21864321
[TBL] [Abstract][Full Text] [Related]
20. [Genetics of migraine].
Freilinger T; Dichgans M
Nervenarzt; 2006 Oct; 77(10):1186, 1188-95. PubMed ID: 16915377
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
