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Interpretation of NOTCH3 mutations in the diagnosis of CADASIL.
Rutten JW, Haan J, Terwindt GM, van Duinen SG, Boon EM, Lesnik Oberstein SA. Rutten JW, et al. Among authors: terwindt gm. Expert Rev Mol Diagn. 2014 Jun;14(5):593-603. doi: 10.1586/14737159.2014.922880. Expert Rev Mol Diagn. 2014. PMID: 24844136 Review.
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.
Genetics of migraine.
Haan J, Terwindt GM, Ferrari MD. Haan J, et al. Among authors: terwindt gm. Neurol Clin. 1997 Feb;15(1):43-60. doi: 10.1016/s0733-8619(05)70294-2. Neurol Clin. 1997. PMID: 9058396 Review.
The quest for migraine genes.
Terwindt GM, Haan J, Ophoff RA, Frants RR, Ferrari MD. Terwindt GM, et al. Curr Opin Neurol. 1997 Jun;10(3):221-5. doi: 10.1097/00019052-199706000-00009. Curr Opin Neurol. 1997. PMID: 9229129 Review.
342 results