A loss-of-function CACNA1A mutation causing benign paroxysmal torticollis of infancy

por Vila-Pueyo, M, Sintas, C, Flotats, M, Gené, G, Elorza, X, Fernández-Fernández, JM, Cormand, B, Macaya, A
Publicado 2013

Screening of cacna1a and ATP1A2 genes in hemiplegic migraine: clinical, genetic and functional studies

por Sintas, C, Carreño, O, Corominas, R, Serra, SA, Vila, M, Fernández-Castillo, N, Toma, C, Pons, R, Llaneza, M, Sobrido, MJ, Grinberg, D, Valverde, MA, Fernández-Fernández, JM, Macaya, A, Cormand, B
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