Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia von Sintas, Cèlia, Carreño, Oriel, Fernàndez-Castillo, Noèlia, Corominas, Roser, Vila-Pueyo, Marta, Toma, Claudio, Cuenca-León, Ester, Barroeta, Isabel, Roig, Carles, Volpini, Víctor, Macaya, Alfons, Cormand, Bru

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Chiari malformation type I: a case-control association study of 58 developmental genes von Urbizu, Aintzane, Toma, Claudio, Poca, Maria A, Sahuquillo, Juan, Cuenca-León, Ester, Cormand, Bru, Macaya, Alfons

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GNAO1 encephalopathy: further delineation of a severe neurodevelopmental syndrome affecting females von Marcé-Grau, Anna, Dalton, James, López-Pisón, Javier, García-Jiménez, María Concepción, Monge-Galindo, Lorena, Cuenca-León, Ester, Giraldo, Jesús, Macaya, Alfons

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Genome-wide DNA methylation analysis in an antimigraine-treated preclinical model of cortical spreading depolarization von Vila-Pueyo, Marta, Cuenca-León, Ester, Queirós, Ana C., Kulis, Marta, Sintas, Cèlia, Cormand, Bru, Martín-Subero, José Ignacio, Pozo-Rosich, Patricia, Fernàndez-Castillo, Noèlia, Macaya, Alfons

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mutation in the first intracellular loop of CACNA1A prevents P/Q channel modulation by SNARE proteins and lowers exocytosis von Serra, Selma A, Cuenca-León, Ester, Llobet, Artur, Rubio-Moscardo, Francisca, Plata, Cristina, Carreño, Oriel, Fernàndez-Castillo, Noèlia, Corominas, Roser, Valverde, Miguel A, Macaya, Alfons, Cormand, Bru, Fernández-Fernández, José M

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The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families von Hiekkala, Marjo Eveliina, Vuola, Pietari, Artto, Ville, Häppölä, Paavo, Häppölä, Elisa, Vepsäläinen, Salli, Cuenca-León, Ester, Lal, Dennis, Gormley, Padhraig, Hämäläinen, Eija, Ilmavirta, Matti, Nissilä, Markku, Säkö, Erkki, Sumelahti, Marja-Liisa, Harno, Hanna, Havanka, Hannele, Keski-Säntti, Petra, Färkkilä, Markus, Palotie, Aarno, Wessman, Maija, Kaunisto, Mari Anneli, Kallela, Mikko

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Two-stage case-control association study of dopamine-related genes and migraine von Corominas, Roser, Ribases, Marta, Camiña, Montserrat, Cuenca-León, Ester, Pardo, Julio, Boronat, Susana, Sobrido, María-Jesús, Cormand, Bru, Macaya, Alfons

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Paroxysmal exercise-induced dyskinesia, writer's cramp, migraine with aura and absence epilepsy in twin brothers with a novel SLC2A1 missense mutation von Urbizu, Aintzane, Cuenca-León, Ester, Raspall-Chaure, Miquel, Gratacòs, Margarida, Conill, Joan, Redecillas, Susana, Roig-Quilis, Manuel, Macaya, Alfons

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Genome-wide DNA methylation analysis in an antimigraine-treated preclinical model of cortical spreading depolarization von Vila-Pueyo, Marta, Cuenca León, Ester, Queirós, Ana C, Kulis, Marta, Sintas Vives, Cèlia, Cormand Rifà, Bru, Martín-Subero, José Ignacio, Pozo-Rosich, Patricia, Fernàndez Castillo, Noèlia, Macaya Ruiz, Alfons

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Habitual sleep disturbances and migraine: a Mendelian randomization study von Guo, Yanjun, Chasman, Daniel I., Saxena, Richa, Gormley, Padhraig, Anttila, Verneri, Winsvold, Bendik S., Palta, Priit, Pers, Tune H., Farh, Kai‐How, Cuenca‐Leon, Ester, Muona, Mikko, Furlotte, Nicholas A., Kurth, Tobias, Ingason, Andres, McMahon, George, Terwindt, Gisela M., Kallela, Mikko, Freilinger, Tobias M., Ran, Caroline, Gordon, Scott G., Stam, Anine H., Steinberg, Stacy, Borck, Guntram, Koiranen, Markku, Quaye, Lydia, Adams, Hieab H. H., Lehtimäki, Terho, Sarin, Antti‐Pekka, Wedenoja, Juho, Buring, Julie E., Ridker, Paul M., Hrafnsdottir, Maria Gudlaug, Stefansson, Hreinn, Ring, Susan M., Hottenga, Jouke‐Jan, Penninx, Brenda W. J. H., Färkkilä, Markus, Artto, Ville, Kaunisto, Mari, Vepsäläinen, Salli, Malik, Rainer, Heath, Andrew C., Madden, Pamela A. F., Kals, Mart, Pärn, Kalle, Hämäläinen, Eija, Huang, Hailiang, Byrnes, Andrea E., Franke, Lude, Huang, Jie, Stergiakouli, Evie, Lee, Phil H., Sandor, Cynthia, Webber, Caleb, Cader, Zameel, Muller‐Myhsok, Bertram, Schreiber, Stefan, Meitinger, Thomas, Eriksson, Johan G., Salomaa, Veikko, Heikkilä, Kauko, Loehrer, Elizabeth, Uitterlinden, Andre G., Hofman, Albert, van Duijn, Cornelia M., Cherkas, Lynn, Pedersen, Linda M., Stubhaug, Audun, Nielsen, Christopher S., Männikkö, Minna, Mihailov, Evelin, Milani, Lili, Göbel, Hartmut, Esserlind, Ann‐Louise, Christensen, Anne Francke, Hansen, Thomas Folkmann, Kaprio, Jaakko, Aromaa, Arpo J., Raitakari, Olli, Ikram, M. Arfan, Spector, Tim, Järvelin, Marjo‐Riitta, Metspalu, Andres, Kubisch, Christian, Strachan, David P., Ferrari, Michel D., Belin, Andrea C., Wessman, Maija, van den Maagdenberg, Arn M. J. M., Zwart, John‐Anker, Boomsma, Dorret I., Smith, George Davey, Stefansson, Kari, Eriksson, Nicholas, Daly, Mark J., Neale, Benjamin M., Olesen, Jes, Chasman, Daniel I., Nyholt, Dale R., Palotie, Aarno

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A causal effects of gut microbiota in the development of migraine von Cormand Rifà, Bru, Cuenca León, Ester, International Headache Genetics Consortium, He, Qiang, Wang, Wenjing, Xiong, Yang, Tao, Chuanyuan, Ma, Lu, Ma, Junpeng, You, Chao

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Paroxysmal non-kinesigenic dyskinesia due to a PNKD recurrent mutation: Report of two Southern European families von Pons, Roser, Cuenca-León, Ester, Miravet, Elena, Pons, Montse, Xaidara, Athina, Youroukos, Sotiris, Macaya, Alfons

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Late-onset episodic ataxia type 2 associated with a novel loss-of-function mutation in the CACNA1A gene von Cuenca-León, Ester, Banchs, Isabel, Serra, Selma A, Latorre, Pilar, Fernàndez-Castillo, Noèlia, Corominas, Roser, Valverde, Miguel A, Volpini, Víctor, Fernández-Fernández, José M, Macaya, Alfons, Cormand, Bru

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Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia von Sintas, Cèlia, Carreño, Oriel, Fernández Castillo, Noelia, Corominas, Roser, Vila Pueyo, Marta, Toma, Claudio, Cuenca-León, Ester, Barroeta, Isabel, Roig, Carles, Volpini, Victor, Macaya, Alfons, Cormand, Bru

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Mutation spectrum in the CACNA1A gene in 49 patients with episodic ataxia von Sintas Vives, Cèlia, Carreño, Oriel, Fernàndez Castillo, Noèlia, Corominas Castiñeira, Roser, Vila Pueyo, Marta, Toma, Claudio, Cuenca León, Ester, Barroeta, Isabel, Roig i Arnall, Carles, Volpini Bertrán, Víctor, Macaya Ruiz, Alfons, Cormand Rifà, Bru

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Mutation spectrum in the CACNA1A gene in 49 patients with episodic ataxia von Sintas Vives, Cèlia, Carreño, Oriel, Fernández Castillo, Noelia, Corominas, Roser, Vila Pueyo, Marta, Toma, Claudio, Cuenca León, Ester, Barroeta, Isabel, Roig, Carles, Volpini Bertrán, Víctor, Macaya Ruiz, Alfons, Cormand Rifà, Bru

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Mutation spectrum in the CACNA1A gene in 49 patients with episodic ataxia von Sintas Vives, Cèlia, Carreño, Oriel, Fernández Castillo, Noelia, Corominas, Roser, Vila Pueyo, Marta, Toma, Claudio, Cuenca León, Ester, Barroeta, Isabel, Roig, Carles, Volpini Bertrán, Víctor, Macaya Ruiz, Alfons, Cormand Rifà, Bru

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Contribution of syntaxin 1A to the genetic susceptibility to migraine: A case–control association study in the Spanish population von Corominas, Roser, Ribasés, Marta, Cuenca-León, Ester, Narberhaus, Bernat, Serra, Selma A., del Toro, Mireia, Roig, Manuel, Fernández-Fernández, José M., Macaya, Alfons, Cormand, Bru

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Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine von Gormley, Padhraig, Anttila, Verneri, Winsvold, Bendik S, Palta, Priit, Esko, Tonu, Pers, Tune H, Farh, Kai-How, Cuenca-Leon, Ester, Furlotte, Nicholas A, Kurth, Tobias, Ingason, Andres, McMahon, George, Ligthart, Lannie, Terwindt, Gisela M, Kallela, Mikko, Freilinger, Tobias M, Ran, Caroline, Gordon, Scott G, Stam, Anine H, Steinberg, Stacy, Borck, Guntram, Koiranen, Markku, Quaye, Lydia, Adams, Hieab H H, Lehtimäki, Terho, Sarin, Antti-Pekka, Wedenoja, Juho, Hinds, David A, Buring, Julie E, Schürks, Markus, Ridker, Paul M, Hrafnsdottir, Maria Gudlaug, Stefansson, Hreinn, Ring, Susan M, Hottenga, Jouke-Jan, Penninx, Brenda W J H, Färkkilä, Markus, Kaunisto, Mari, Vepsäläinen, Salli, Malik, Rainer, Heath, Andrew C, Madden, Pamela A F, Martin, Nicholas G, Kurki, Mitja I, Kals, Mart, Mägi, Reedik, Pärn, Kalle, Hämäläinen, Eija, Huang, Hailiang, Byrnes, Andrea E, Franke, Lude, Huang, Jie, Stergiakouli, Evie, Lee, Phil H, Sandor, Cynthia, Webber, Caleb, Cader, Zameel, Muller-Myhsok, Bertram, Schreiber, Stefan, Meitinger, Thomas, Eriksson, Johan G, Salomaa, Veikko, Heikkilä, Kauko, Loehrer, Elizabeth, Uitterlinden, Andre G, Hofman, Albert, van Duijn, Cornelia M, Cherkas, Lynn, Pedersen, Linda M, Stubhaug, Audun, Nielsen, Christopher S, Männikkö, Minna, Mihailov, Evelin, Milani, Lili, Göbel, Hartmut, Esserlind, Ann-Louise, Christensen, Anne Francke, Werge, Thomas, Kaprio, Jaakko, Aromaa, Arpo J, Raitakari, Olli, Ikram, M Arfan, Spector, Tim, Järvelin, Marjo-Riitta, Metspalu, Andres, Kubisch, Christian, Strachan, David P, Dichgans, Martin, Wessman, Maija, Zwart, John-Anker, Boomsma, Dorret I, Smith, George Davey, Stefansson, Kari, Eriksson, Nicholas, Daly, Mark J, Neale, Benjamin M, Olesen, Jes, Chasman, Daniel I, Nyholt, Dale R, Palotie, Aarno

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Chiari malformation type I: a case-control association study of 58 developmental genes von Urbizu Serrano, Aintzane, Toma, Claudio, Poca Pastor, María Antonia, Sahuquillo, Juan, Cuenca León, Ester, Cormand Rifà, Bru, Macaya Ruiz, Alfons

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