Novel SCN1A mutation in the IFMT motif of the α1 subunit of the voltage-gated NaV1.1 channel causing familial hemiplegic migraine

por De Vries, B, Weller, CM, De Fàbregues, O, Koelewijn, SC, Stam, AH, Haan, J, Ferrari, MD, Terwindt, GM, van den Maagdenberg, AMJ
Publicado 2013

Corticosterone enhances CSD susceptibility via glucocorticoid receptor activation in familial hemiplegic migraine 1 Cacna1a knock-in mice

por Shyti, R, Eikermann-Haerter, K, Meijer, OC, van Heiningen, SH, De Groote, L, Ferrari, MD, Ayata, C, van den Maagdenberg, AMJ, Tolner, EA
Publicado 2013

Migraine without aura: genome-wide association analysis identifies several novel susceptibility

por De Vries, B Loci, Freilinger, T, Anttila, V, Malik, R, Terwindt, GM, Pozo-Rosich, P, Winsvold, B, Nyholt, D, van Oosterhout, WPJ, Artto, V, Todt, M, Hämäläinen, E, Fernandez-Moralez, J, Louter, M, Kaunisto, MA, Schoenen, J, Raitakari, O, Lehtimäki, T, Ville-Pueyo, M, Göbel, H, Wichman, E, Sintas, C, Uitterlinden, A, Hofman, A, Rivadeneira, F, Heinze, A, Tronvik, E, van Duin, CM, Kaprio, J, Cormand, B, Wessman, M, Frants, RR, Meitinger, T, Müller-Myhsok, B, Zwart, JA, Färkkilä, M, Macaya, A, Ferrari, MD, Kubisch, C, Palotie, A, Dichgans, M, van den Maagdenberg, AMJ
Publicado 2013