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16. Clinical aspects of familial hemiplegic migraine in two families. O'Hare JA; Feely MJ; Callaghan N Ir Med J; 1981 Oct; 74(10):291-5. PubMed ID: 7309446 [No Abstract] [Full Text] [Related]
19. Functional consequences of mutations in the human alpha1A calcium channel subunit linked to familial hemiplegic migraine. Hans M; Luvisetto S; Williams ME; Spagnolo M; Urrutia A; Tottene A; Brust PF; Johnson EC; Harpold MM; Stauderman KA; Pietrobon D J Neurosci; 1999 Mar; 19(5):1610-9. PubMed ID: 10024348 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]