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The impact of pharmacogenetics for migraine.
Ophoff RA, van den Maagdenberg AM, Roon KI, Ferrari MD, Frants RR. Ophoff RA, et al. Among authors: van den maagdenberg am. Eur J Pharmacol. 2001 Feb 9;413(1):1-10. doi: 10.1016/s0014-2999(00)00949-3. Eur J Pharmacol. 2001. PMID: 11173058 Review.
Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3.
Ophoff RA, DeYoung J, Service SK, Joosse M, Caffo NA, Sandkuijl LA, Terwindt GM, Haan J, van den Maagdenberg AM, Jen J, Baloh RW, Barilla-LaBarca ML, Saccone NL, Atkinson JP, Ferrari MD, Freimer NB, Frants RR. Ophoff RA, et al. Among authors: van den maagdenberg am. Am J Hum Genet. 2001 Aug;69(2):447-53. doi: 10.1086/321975. Epub 2001 Jun 28. Am J Hum Genet. 2001. PMID: 11438888 Free PMC article.
Mutant P/Q-type calcium channel electrophysiology and migraine.
Plomp JJ, van den Maagdenberg AM, Molenaar PC, Frants RR, Ferrari MD. Plomp JJ, et al. Among authors: van den maagdenberg am. Curr Opin Investig Drugs. 2001 Sep;2(9):1250-60. Curr Opin Investig Drugs. 2001. PMID: 11717812 Review.
Calcium channel mutations and migraine.
Kors EE, van den Maagdenberg AM, Plomp JJ, Frants RR, Ferrari MD. Kors EE, et al. Among authors: van den maagdenberg am. Curr Opin Neurol. 2002 Jun;15(3):311-6. doi: 10.1097/00019052-200206000-00014. Curr Opin Neurol. 2002. PMID: 12045730 Review.
330 results