Familial Hemiplegic Migraine

Ducros A, Denier C, Joutel A, et al. The clinical spectrum of Familial Hemiplegic Migraine associated with mutations in a neuronal calcium channel. N Engl J Med 2001;345:17-24.

Ducros A, Joutel A, Vahedi K, Cecillon M, Ferreira A, Bernard E, et al. Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity. Ann Neurol 1997;42:885-890.

Joutel A, Bousser MG, Biousse V, Labauge P, Chabriat H, Nibbio A, et al. A gene for familial hemiplegic migraine maps to chromosome 19. Nature Genet 1993;5:40-45.

Ophoff RA, Terwindt GM, Vergouwe MN, et al. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4. Cell 1996;87:543-552.

Terwindt GM, Ophoff RA, Haan J, Sandkuijl LA, Frants RR, Ferrari MD. Migraine, ataxia and epilepsy: a challenging spectrum of genetically determined calcium channelopathies. Eur J Hum Genet 1998;6:297-307.

Thomsen LL, Eriksen MK, Roemer SF, Andersen I, Oleson J, Russell MB. A population-based study of familial hemiplegic migraine suggests revised diagnostic criteria Brain 2002;125:1379-1391.

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