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Migraine and genetic and acquired vasculopathies.
Stam AH, Haan J, van den Maagdenberg AM, Ferrari MD, Terwindt GM. Stam AH, et al. Among authors: terwindt gm. Cephalalgia. 2009 Sep;29(9):1006-17. doi: 10.1111/j.1468-2982.2009.01940.x. Cephalalgia. 2009. PMID: 19689610 Review.
Association study in migraine.
Terwindt GM, Ferrari MD. Terwindt GM, et al. Cephalalgia. 1995 Jun;15(3):163. doi: 10.1046/j.1468-2982.1995.015003163.x. Cephalalgia. 1995. PMID: 7553801 No abstract available.
Genetic heterogeneity of familial hemiplegic migraine.
Ophoff RA, van Eijk R, Sandkuijl LA, Terwindt GM, Grubben CP, Haan J, Lindhout D, Ferrari MD, Frants RR. Ophoff RA, et al. Among authors: terwindt gm. Genomics. 1994 Jul 1;22(1):21-6. doi: 10.1006/geno.1994.1340. Genomics. 1994. PMID: 7959770
Is familial hemiplegic migraine a hereditary form of basilar migraine?
Haan J, Terwindt GM, Ophoff RA, Bos PL, Frants RR, Ferrari MD, Krommenhoek T, Lindhout DL, Sandkuyl LA, Van Eyk R. Haan J, et al. Among authors: terwindt gm. Cephalalgia. 1995 Dec;15(6):477-81. doi: 10.1046/j.1468-2982.1995.1506477.x. Cephalalgia. 1995. PMID: 8706110 Clinical Trial.
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
Ophoff RA, Terwindt GM, Vergouwe MN, van Eijk R, Oefner PJ, Hoffman SM, Lamerdin JE, Mohrenweiser HW, Bulman DE, Ferrari M, Haan J, Lindhout D, van Ommen GJ, Hofker MH, Ferrari MD, Frants RR. Ophoff RA, et al. Among authors: terwindt gm. Cell. 1996 Nov 1;87(3):543-52. doi: 10.1016/s0092-8674(00)81373-2. Cell. 1996. PMID: 8898206 Free article.
345 results