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4. 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]
5. Next-generation sequencing identified a novel CACNA1A I1379F variant in a familial hemiplegic migraine type 1 pedigree: A case report. Luan H; Zhang L; Zhang S; Zhang M Medicine (Baltimore); 2021 Dec; 100(51):e28141. PubMed ID: 34941060 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group. Terwindt GM; Ophoff RA; Haan J; Vergouwe MN; van Eijk R; Frants RR; Ferrari MD Neurology; 1998 Apr; 50(4):1105-10. PubMed ID: 9566402 [TBL] [Abstract][Full Text] [Related]
8. 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]
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10. 1H-MRS alterations in the cerebellum of patients with familial hemiplegic migraine type 1. Dichgans M; Herzog J; Freilinger T; Wilke M; Auer DP Neurology; 2005 Feb; 64(4):608-13. PubMed ID: 15728280 [TBL] [Abstract][Full Text] [Related]
11. Familial hemiplegic migraine, nystagmus, and cerebellar atrophy. Elliott MA; Peroutka SJ; Welch S; May EF Ann Neurol; 1996 Jan; 39(1):100-6. PubMed ID: 8572654 [TBL] [Abstract][Full Text] [Related]
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13. 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]
14. 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]
15. [Hemiplegic migraine complicated with coronary vasospasm]. Takeuchi I; Hata T; Itagaki H; Akutsu T; Takagi Y Rinsho Shinkeigaku; 1992 Jan; 32(1):73-7. PubMed ID: 1628439 [TBL] [Abstract][Full Text] [Related]
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