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44. New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: migraine as the prominent clinical feature. Vérin M; Rolland Y; Landgraf F; Chabriat H; Bompais B; Michel A; Vahedi K; Martinet JP; Tournier-Lasserve E; Lemaitre MH J Neurol Neurosurg Psychiatry; 1995 Dec; 59(6):579-85. PubMed ID: 7500094 [TBL] [Abstract][Full Text] [Related]
45. Intracellular and plasma magnesium in familial hemiplegic migraine and migraine with and without aura. Smeets MC; Vernooy CB; Souverijn JH; Ferrari MD Cephalalgia; 1994 Feb; 14(1):29-32. PubMed ID: 8200020 [TBL] [Abstract][Full Text] [Related]
46. CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhood. de Vries B; Stam AH; Beker F; van den Maagdenberg AM; Vanmolkot KR; Laan L; Ginjaar IB; Frants RR; Lauffer H; Haan J; Haas JP; Terwindt GM; Ferrari MD Cephalalgia; 2008 Aug; 28(8):887-91. PubMed ID: 18498393 [TBL] [Abstract][Full Text] [Related]
48. Wolff Award 1997. Involvement of a Ca2+ channel gene in familial hemiplegic migraine and migraine with and without aura. Dutch Migraine Genetics Research Group. Ophoff RA; Terwindt GM; Vergouwe MN; Frants RR; Ferrari MD Headache; 1997 Sep; 37(8):479-85. PubMed ID: 9329229 [TBL] [Abstract][Full Text] [Related]
49. Episodic ataxia and channelopathies. Gordon N Brain Dev; 1998 Jan; 20(1):9-13. PubMed ID: 9533553 [TBL] [Abstract][Full Text] [Related]
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53. Mitral valve prolapse and platelet aggregation in patients with hemiplegic and non-hemiplegic migraine. Pfaffenrath V; Pöllmann W; Autenrieth G; Rosmanith U Acta Neurol Scand; 1987 Apr; 75(4):253-7. PubMed ID: 3591274 [TBL] [Abstract][Full Text] [Related]
54. Novel Presentation of Hemiplegic Migraine in a Patient With Cockayne Syndrome. Carroll J; Pabst L; Koboldt DC; Franklin SJ; Choi S; Wilson RK; Lo W Pediatr Neurol; 2023 Jan; 138():95-97. PubMed ID: 36434915 [TBL] [Abstract][Full Text] [Related]
55. Acute striatal necrosis in hemiplegic migraine with de novo CACNA1A mutation. Carreño O; García-Silva MT; García-Campos Ó; Martínez-de Aragón A; Cormand B; Macaya A Headache; 2011; 51(10):1542-6. PubMed ID: 22082423 [TBL] [Abstract][Full Text] [Related]
56. Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family. Alonso I; Barros J; Tuna A; Coelho J; Sequeiros J; Silveira I; Coutinho P Arch Neurol; 2003 Apr; 60(4):610-4. PubMed ID: 12707077 [TBL] [Abstract][Full Text] [Related]
57. Current status of genetic discoveries in migraine: familial hemiplegic migraine and beyond. Gardner K; Hoffman EP Curr Opin Neurol; 1998 Jun; 11(3):211-6. PubMed ID: 9642538 [TBL] [Abstract][Full Text] [Related]
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60. 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] [Previous] [Next] [New Search]