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4. Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine. Kors EE; Terwindt GM; Vermeulen FL; Fitzsimons RB; Jardine PE; Heywood P; Love S; van den Maagdenberg AM; Haan J; Frants RR; Ferrari MD Ann Neurol; 2001 Jun; 49(6):753-60. PubMed ID: 11409427 [TBL] [Abstract][Full Text] [Related]
5. Wide clinical variability in a family with a CACNA1A T666m mutation: hemiplegic migraine, coma, and progressive ataxia. Wada T; Kobayashi N; Takahashi Y; Aoki T; Watanabe T; Saitoh S Pediatr Neurol; 2002 Jan; 26(1):47-50. PubMed ID: 11814735 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. A wide spectrum of clinical, neurophysiological and neuroradiological abnormalities in a family with a novel CACNA1A mutation. Romaniello R; Zucca C; Tonelli A; Bonato S; Baschirotto C; Zanotta N; Epifanio R; Righini A; Bresolin N; Bassi MT; Borgatti R J Neurol Neurosurg Psychiatry; 2010 Aug; 81(8):840-3. PubMed ID: 20682717 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. [Genetics of migraine]. Ducros A Pathol Biol (Paris); 2000 Sep; 48(7):658-62. PubMed ID: 11072644 [TBL] [Abstract][Full Text] [Related]
12. Downbeat positioning nystagmus is a common clinical feature despite variable phenotypes in an FHM1 family. Yabe I; Kitagawa M; Suzuki Y; Fujiwara K; Wada T; Tsubuku T; Takeichi N; Sakushima K; Soma H; Tsuji S; Niino M; Saitoh S; Sasaki H J Neurol; 2008 Oct; 255(10):1541-4. PubMed ID: 18670797 [TBL] [Abstract][Full Text] [Related]
15. The prevalence of familial hemiplegic migraine with cerebellar ataxia and spinocerebellar ataxia type 6 in Portugal. Barros J; Ruano L; Domingos J; Tuna A; Damásio J; Alonso I; Silveira I; Sequeiros J; Coutinho P Headache; 2014 May; 54(5):911-5. PubMed ID: 24898624 [TBL] [Abstract][Full Text] [Related]
16. Sporadic hemiplegic migraine and delayed cerebral oedema after minor head trauma: a novel de novo CACNA1A gene mutation. Malpas TJ; Riant F; Tournier-Lasserve E; Vahedi K; Neville BG Dev Med Child Neurol; 2010 Jan; 52(1):103-4. PubMed ID: 19811514 [No 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. [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]
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20. Two distinct phenotypes, hemiplegic migraine and episodic Ataxia type 2, caused by a novel common CACNA1A variant. Nardello R; Plicato G; Mangano GD; Gennaro E; Mangano S; Brighina F; Raieli V; Fontana A BMC Neurol; 2020 Apr; 20(1):155. PubMed ID: 32336275 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]