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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]
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]
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]