306 related articles for article (PubMed ID: 17502463)
1. Genetic models of migraine.
van de Ven RC; Kaja S; Plomp JJ; Frants RR; van den Maagdenberg AM; Ferrari MD
Arch Neurol; 2007 May; 64(5):643-6. PubMed ID: 17502463
[TBL] [Abstract][Full Text] [Related]
2. Familial hemiplegic migraine.
Hansen JM
Dan Med Bull; 2010 Sep; 57(9):B4183. PubMed ID: 20816023
[TBL] [Abstract][Full Text] [Related]
3. Migraine, ataxia and epilepsy: a challenging spectrum of genetically determined calcium channelopathies. Dutch Migraine Genetics Research Group.
Terwindt GM; Ophoff RA; Haan J; Sandkuijl LA; Frants RR; Ferrari MD
Eur J Hum Genet; 1998; 6(4):297-307. PubMed ID: 9781035
[TBL] [Abstract][Full Text] [Related]
4. [Genetics of migraine].
Ducros A
Pathol Biol (Paris); 2000 Sep; 48(7):658-62. PubMed ID: 11072644
[TBL] [Abstract][Full Text] [Related]
5. [From gene to disease; from CACNA1A to migraine].
Kors EE; Haan J; Frants RR; Ferrari MD
Ned Tijdschr Geneeskd; 2001 Feb; 145(6):266-7. PubMed ID: 11236374
[TBL] [Abstract][Full Text] [Related]
6. The FHM1 mutation S218L: a severe clinical phenotype? A case report and review of the literature.
Debiais S; Hommet C; Bonnaud I; Barthez MA; Rimbaux S; Riant F; Autret A
Cephalalgia; 2009 Dec; 29(12):1337-9. PubMed ID: 19438926
[TBL] [Abstract][Full Text] [Related]
7. FHM3 in familial hemiplegic migraine is more resistant to mutation than FHM1 and FHM2.
Wiwanitkit V
J Neurol Sci; 2009 Feb; 277(1-2):76-9. PubMed ID: 19007941
[TBL] [Abstract][Full Text] [Related]
8. CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine.
Stam AH; Vanmolkot KR; Kremer HP; Gärtner J; Brown J; Leshinsky-Silver E; Gilad R; Kors EE; Frankhuizen WS; Ginjaar HB; Haan J; Frants RR; Ferrari MD; van den Maagdenberg AM; Terwindt GM
Clin Genet; 2008 Nov; 74(5):481-5. PubMed ID: 18400034
[TBL] [Abstract][Full Text] [Related]
9. [Familial hemiplegic migraine resulting in recurrent coma].
Lee H; Aramideh M; Ginjaar HB
Ned Tijdschr Geneeskd; 2008 Feb; 152(7):393-6. PubMed ID: 18380388
[TBL] [Abstract][Full Text] [Related]
10. Sporadic hemiplegic migraine and epilepsy associated with CACNA1A gene mutation.
Zangaladze A; Asadi-Pooya AA; Ashkenazi A; Sperling MR
Epilepsy Behav; 2010 Feb; 17(2):293-5. PubMed ID: 20071244
[TBL] [Abstract][Full Text] [Related]
11. 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. PubMed ID: 17142831
[TBL] [Abstract][Full Text] [Related]
12. Familial hemiplegic migraine: more than just a headache.
Benatar M; Ford CC
Neurology; 2005 Feb; 64(4):592-3. PubMed ID: 15728276
[No Abstract] [Full Text] [Related]
13. Is the CACNA1A gene involved in familial migraine with aura?
Brugnoni R; Leone M; Rigamonti A; Moranduzzo E; Cornelio F; Mantegazza R; Bussone G
Neurol Sci; 2002 Apr; 23(1):1-5. PubMed ID: 12111613
[TBL] [Abstract][Full Text] [Related]
14. Minor head trauma-induced sporadic hemiplegic migraine coma.
Curtain RP; Smith RL; Ovcaric M; Griffiths LR
Pediatr Neurol; 2006 Apr; 34(4):329-32. PubMed ID: 16638514
[TBL] [Abstract][Full Text] [Related]
15. The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.
Ducros A; Denier C; Joutel A; Cecillon M; Lescoat C; Vahedi K; Darcel F; Vicaut E; Bousser MG; Tournier-Lasserve E
N Engl J Med; 2001 Jul; 345(1):17-24. PubMed ID: 11439943
[TBL] [Abstract][Full Text] [Related]
16. Basilar-type migraine: clinical, epidemiologic, and genetic features.
Kirchmann M; Thomsen LL; Olesen J
Neurology; 2006 Mar; 66(6):880-6. PubMed ID: 16567706
[TBL] [Abstract][Full Text] [Related]
17. Migraine: gene mutations and functional consequences.
van den Maagdenberg AM; Haan J; Terwindt GM; Ferrari MD
Curr Opin Neurol; 2007 Jun; 20(3):299-305. PubMed ID: 17495624
[TBL] [Abstract][Full Text] [Related]
18. Electroencephalographic changes and seizures in familial hemiplegic migraine patients with the CACNA1A gene S218L mutation.
Chan YC; Burgunder JM; Wilder-Smith E; Chew SE; Lam-Mok-Sing KM; Sharma V; Ong BK
J Clin Neurosci; 2008 Aug; 15(8):891-4. PubMed ID: 18313928
[TBL] [Abstract][Full Text] [Related]
19. 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. PubMed ID: 17877748
[TBL] [Abstract][Full Text] [Related]
20. Familial hemiplegic migraine presenting as recurrent encephalopathy in a Native Indian family.
Spacey SD; Vanmolkot KR; Murphy C; van den Maagdenberg AM; Hsiung RG
Headache; 2005 Oct; 45(9):1244-9. PubMed ID: 16178956
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
