Apoptosis in substantia nigra following developmental striatal excitotoxic injury.

Por Macaya, A, Munell, F, Gubits, R M, Burke, R E
Publicado em 1994

EHMTI-0048. Epigenetic changes in a rat model of migraine with aura

Por Vila-Pueyo, M, Fernández-Castillo, N, Cormand, B, Pozo-Rosich, P, Macaya, A
Publicado em 2014

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 em 2013

Congenital insensitivity to pain with anhidrosis: novel mutations in the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor.

Por Mardy, S, Miura, Y, Endo, F, Matsuda, I, Sztriha, L, Frossard, P, Moosa, A, Ismail, E A, Macaya, A, Andria, G, Toscano, E, Gibson, W, Graham, G E, Indo, Y
Publicado em 1999

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 em 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 em 2013