These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

206 related articles for article (PubMed ID: 18279427)

  • 1. Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation.
    Freilinger T; Bohe M; Wegener B; Müller-Myhsok B; Dichgans M; Knoblauch H
    Cephalalgia; 2008 Apr; 28(4):403-7. PubMed ID: 18279427
    [No Abstract]   [Full Text] [Related]  

  • 2. Stepwise developmental regression associated with novel CACNA1A mutation.
    Guerin AA; Feigenbaum A; Donner EJ; Yoon G
    Pediatr Neurol; 2008 Nov; 39(5):363-4. PubMed ID: 18940563
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. [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]  

  • 5. Cerebellar ataxia, hemiplegic migraine, and related phenotypes due to a CACNA1A missense mutation: 12-year follow-up of a large Portuguese family.
    Barros J; Damásio J; Tuna A; Alves I; Silveira I; Pereira-Monteiro J; Sequeiros J; Alonso I; Sousa A; Coutinho P
    JAMA Neurol; 2013 Feb; 70(2):235-40. PubMed ID: 23407676
    [TBL] [Abstract][Full Text] [Related]  

  • 6. CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy.
    Vahedi K; Denier C; Ducros A; Bousson V; Levy C; Chabriat H; Haguenau M; Tournier-Lasserve E; Bousser MG
    Neurology; 2000 Oct; 55(7):1040-2. PubMed ID: 11061267
    [TBL] [Abstract][Full Text] [Related]  

  • 7. CACNA1A nonsense mutation is associated with basilar-type migraine and episodic ataxia type 2.
    Robbins MS; Lipton RB; Laureta EC; Grosberg BM
    Headache; 2009 Jul; 49(7):1042-6. PubMed ID: 19486177
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. Familial hemiplegic migraine with prolonged coma and cerebellar atrophy: CACNA1A T666M mutation in a Korean family.
    Choi KH; Kim JS; Lee SY; Ryu SW; Kim SS; Lee SH; Kim S; Park HK
    J Korean Med Sci; 2012 Sep; 27(9):1124-7. PubMed ID: 22969264
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 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. Early-onset cerebellar atrophy associated with mutation in the CACNA1A gene.
    Naik S; Pohl K; Malik M; Siddiqui A; Josifova D
    Pediatr Neurol; 2011 Nov; 45(5):328-30. PubMed ID: 22000314
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraine.
    Kors EE; Haan J; Giffin NJ; Pazdera L; Schnittger C; Lennox GG; Terwindt GM; Vermeulen FL; Van den Maagdenberg AM; Frants RR; Ferrari MD
    Arch Neurol; 2003 May; 60(5):684-8. PubMed ID: 12756131
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Genetics of migraine].
    Ducros A
    Pathol Biol (Paris); 2000 Sep; 48(7):658-62. PubMed ID: 11072644
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine.
    Terwindt G; Kors E; Haan J; Vermeulen F; Van den Maagdenberg A; Frants R; Ferrari M
    Arch Neurol; 2002 Jun; 59(6):1016-8. PubMed ID: 12056940
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Two novel functional mutations in the Na+,K+-ATPase alpha2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes.
    Castro MJ; Nunes B; de Vries B; Lemos C; Vanmolkot KR; van den Heuvel JJ; Temudo T; Barros J; Sequeiros J; Frants RR; Koenderink JB; Pereira-Monteiro JM; van den Maagdenberg AM
    Clin Genet; 2008 Jan; 73(1):37-43. PubMed ID: 18028456
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Possible effect of corticoids on hemiplegic attacks in severe hemiplegic migraine.
    Sánchez-Albisua I; Schöning M; Jurkat-Rott K; Lerche H
    Pediatr Neurol; 2013 Oct; 49(4):286-8. PubMed ID: 23831250
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel mutation in CACNA1A associated with hemiplegic migraine, cerebellar dysfunction and late-onset cognitive decline.
    Freilinger T; Ackl N; Ebert A; Schmidt C; Rautenstrauss B; Dichgans M; Danek A
    J Neurol Sci; 2011 Jan; 300(1-2):160-3. PubMed ID: 21035146
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.