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 *

145 related articles for article (PubMed ID: 9741473)

  • 21. A novel nonsense mutation in CACNA1A causes episodic ataxia and hemiplegia.
    Jen J; Yue Q; Nelson SF; Yu H; Litt M; Nutt J; Baloh RW
    Neurology; 1999 Jul; 53(1):34-7. PubMed ID: 10408533
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
    Ophoff RA; Terwindt GM; Vergouwe MN; van Eijk R; Oefner PJ; Hoffman SM; Lamerdin JE; Mohrenweiser HW; Bulman DE; Ferrari M; Haan J; Lindhout D; van Ommen GJ; Hofker MH; Ferrari MD; Frants RR
    Cell; 1996 Nov; 87(3):543-52. PubMed ID: 8898206
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. 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]  

  • 25. Familial hemiplegic migraine: involvement of a calcium neuronal channel.
    Ophoff RA; Terwindt GM; Vergouwe MN; Frants RR; Ferrari MD
    Neurologia; 1997 Dec; 12 Suppl 5():31-7. PubMed ID: 9436352
    [TBL] [Abstract][Full Text] [Related]  

  • 26. No involvement of the calcium channel gene (CACNA1A) in a family with cluster headache.
    Haan J; van Vliet JA; Kors EE; Terwindt GM; Vermeulen FL; van den Maagdenberg AM; Frants RR; Ferrari MD
    Cephalalgia; 2001 Dec; 21(10):959-62. PubMed ID: 11843867
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Absence of known familial hemiplegic migraine (FHM) mutations in the CACNA1A gene in patients with common migraine: implications for genetic testing.
    Wieser T; Mueller C; Evers S; Zierz S; Deufel T
    Clin Chem Lab Med; 2003 Mar; 41(3):272-5. PubMed ID: 12705332
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Neurotology of migraine.
    Baloh RW
    Headache; 1997; 37(10):615-21. PubMed ID: 9439080
    [TBL] [Abstract][Full Text] [Related]  

  • 29. New CACNA1A deletions are associated to migraine phenotypes.
    Grieco GS; Gagliardi S; Ricca I; Pansarasa O; Neri M; Gualandi F; Nappi G; Ferlini A; Cereda C
    J Headache Pain; 2018 Aug; 19(1):75. PubMed ID: 30167989
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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. PubMed ID: 18513263
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Congenital ataxia and hemiplegic migraine with cerebral edema associated with a novel gain of function mutation in the calcium channel CACNA1A.
    García Segarra N; Gautschi I; Mittaz-Crettol L; Kallay Zetchi C; Al-Qusairi L; Van Bemmelen MX; Maeder P; Bonafé L; Schild L; Roulet-Perez E
    J Neurol Sci; 2014 Jul; 342(1-2):69-78. PubMed ID: 24836863
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Episodic vertigo: central nervous system causes.
    Baloh RW
    Curr Opin Neurol; 2002 Feb; 15(1):17-21. PubMed ID: 11796946
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Missense CACNA1A mutation causing episodic ataxia type 2.
    Denier C; Ducros A; Durr A; Eymard B; Chassande B; Tournier-Lasserve E
    Arch Neurol; 2001 Feb; 58(2):292-5. PubMed ID: 11176968
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Molecular genetic findings in migraine].
    Østergaard E; Thomsen LL; Russell MB
    Ugeskr Laeger; 2001 Nov; 163(45):6260-5. PubMed ID: 11723684
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Familial benign recurrent vertigo.
    Oh AK; Lee H; Jen JC; Corona S; Jacobson KM; Baloh RW
    Am J Med Genet; 2001 May; 100(4):287-91. PubMed ID: 11343320
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Link between confusional migraine, hemiplegic migraine and episodic ataxia type 2: hypothesis, family genealogy, gene typing and classification.
    Cleves C; Parikh S; Rothner AD; Tepper SJ
    Cephalalgia; 2010 Jun; 30(6):740-3. PubMed ID: 19624685
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. [Role of P/Q calcium channel in familial hemiplegic migraine].
    Weiss N; Tournier-Lasserve E; De Waard M
    Med Sci (Paris); 2007 Jan; 23(1):53-63. PubMed ID: 17212932
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [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]  

  • 40. Eye movement disorders are an early manifestation of CACNA1A mutations in children.
    Tantsis EM; Gill D; Griffiths L; Gupta S; Lawson J; Maksemous N; Ouvrier R; Riant F; Smith R; Troedson C; Webster R; Menezes MP
    Dev Med Child Neurol; 2016 Jun; 58(6):639-44. PubMed ID: 26814174
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.