Análisis socio-técnico de los regímenes de promoción industrial de 1944 y 1958 en el sector automotriz en Argentina von Picabea, Facundo, Urcelay, Florencia E.

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Common variants at PVT1, ATG13–AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency von Bronson, Paola G, Chang, Diana, Bhangale, Tushar, Seldin, Michael F, Ortmann, Ward, Ferreira, Ricardo C, Urcelay, Elena, Pereira, Luis Fernández, Martin, Javier, Plebani, Alessandro, Lougaris, Vassilios, Friman, Vanda, Freiberger, Tomáš, Litzman, Jiri, Thon, Vojtech, Pan-Hammarström, Qiang, Hammarström, Lennart, Graham, Robert R, Behrens, Timothy W

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Response to Jabalameli von Urcelay, E

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The autoimmune disease-associated KIF5A, CD226 and SH2B3 gene variants confer susceptibility for multiple sclerosis von Alcina, A, Vandenbroeck, K, Otaegui, D, Saiz, A, Gonzalez, J R, Fernandez, O, Cavanillas, M L, Cénit, M C, Arroyo, R, Alloza, I, García-Barcina, M, Antigüedad, A, Leyva, L, Izquierdo, G, Lucas, M, Fedetz, M, Pinto-Medel, M J, Olascoaga, J, Blanco, Y, Comabella, M, Montalban, X, Urcelay, E, Matesanz, F

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Chitinase 3-like 1 plasma levels are increased in patients with progressive forms of multiple sclerosis von Cantó, E, Reverter, F, Morcillo-Suárez, C, Matesanz, F, Fernández, O, Izquierdo, G, Vandenbroeck, K, Rodríguez-Antigüedad, A, Urcelay, E, Arroyo, R, Otaegui, D, Olascoaga, J, Saiz, A, Navarro, A, Sanchez, A, Domínguez, C, Caminero, A, Horga, A, Tintoré, M, Montalban, X, Comabella, M

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Role of TNFRSF1B polymorphisms in the response of Crohn’s disease patients to infliximab von Medrano, L.M, Taxonera, C, Márquez, A, Barreiro-de Acosta, M, Gómez-García, M, González-Artacho, C, Pérez-Calle, J.L, Bermejo, F, Lopez-Sanromán, A, Martín Arranz, M.D, Gisbert, J.P, Mendoza, J.L, Martín, J, Urcelay, E, Núñez, C

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STAT3 locus in inflammatory bowel disease and multiple sclerosis susceptibility von Cénit, M C, Alcina, A, Márquez, A, Mendoza, J L, Díaz-Rubio, M, de las Heras, V, Izquierdo, G, Arroyo, R, Fernández, O, de la Concha, E G, Matesanz, F, Urcelay, E

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Chromosomal region 16p13: further evidence of increased predisposition to immune diseases von Martínez, A, Perdigones, N, Cénit, M C, Espino, L, Varadé, J, Lamas, J R, Santiago, J L, Fernández-Arquero, M, de la Calle, H, Arroyo, R, de la Concha, E G, Fernández-Gutiérrez, B, Urcelay, E

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ANKRD55 and DHCR7 are novel multiple sclerosis risk loci von Alloza, I, Otaegui, D, de Lapuente, A Lopez, Antigüedad, A, Varadé, J, Núñez, C, Arroyo, R, Urcelay, E, Fernandez, O, Leyva, L, Fedetz, M, Izquierdo, G, Lucas, M, Oliver-Martos, B, Alcina, A, Saiz, A, Blanco, Y, Comabella, M, Montalban, X, Olascoaga, J, Matesanz, F, Vandenbroeck, K

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PADI4 polymorphisms are not associated with rheumatoid arthritis in the Spanish population von Martinez, A., Valdivia, A., Pascual-Salcedo, D., Lamas, J. Ramón, Fernández-Arquero, M., Balsa, A., Fernández-Gutiérrez, B., de la Concha, E. G., Urcelay, E.

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MHC2TA rs4774C and HHV-6A active replication in multiple sclerosis patients von Alvarez-Lafuente, R., Martinez, A., Garcia-Montojo, M., Mas, A., De Las Heras, V., Dominguez-Mozo, M. I., Maria del Carmen, C., López-Cavanillas, M., Bartolome, M., Gomez de la Concha, E., Urcelay, E., Arroyo, R.

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Glypican 5 is an interferon-beta response gene: a replication study von Cénit, MDC, Blanco-Kelly, F, de las Heras, V, Bartolomé, M, de la Concha, EG, Urcelay, E, Arroyo, R, Martínez, A

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Toll-like receptor-9 in Spanish multiple sclerosis patients: an association with the gender von Dominguez-Mozo, M. I., Garcia-Montojo, M., López-Cavanillas, M., De Las Heras, V., Garcia-Martinez, A., Arias-Leal, A. M., Casanova, I., Urcelay, E., Arroyo, R., Alvarez-Lafuente, R.

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Validation of IRF5 as multiple sclerosis risk gene: putative role in interferon beta therapy and human herpes virus-6 infection von Vandenbroeck, K, Alloza, I, Swaminathan, B, Antigüedad, A, Otaegui, D, Olascoaga, J, Barcina, M G, de las Heras, V, Bartolomé, M, Fernández-Arquero, M, Arroyo, R, Alvarez-Lafuente, R, Cénit, M C, Urcelay, E

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IL23R: a susceptibility locus for celiac disease and multiple sclerosis? von Núñez, C, Dema, B, Cénit, M C, Polanco, I, Maluenda, C, Arroyo, R, de las Heras, V, Bartolomé, M, de la Concha, E G, Urcelay, E, Martínez, A

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Association of the IFIH1-GCA-KCNH7 chromosomal region with rheumatoid arthritis von Martínez, A, Varadé, J, Lamas, J R, Fernández-Arquero, M, Jover, J A, de la Concha, E G, Fernández-Gutiérrez, B, Urcelay, E

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Analysis of the IL28RA locus as genetic risk factor for multiple sclerosis von Lopez de Lapuente, A, Alloza, I, Goertsches, R, Zettl, U.K, Urcelay, E, Arroyo, R, Comabella, M, Montalban, X, Antigüedad, A, Vandenbroeck, K

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A functional variant in the CD209 promoter is associated with DQ2-negative celiac disease in the Spanish population von Núñez, C, Rueda, B, Martínez, A, Maluenda, C, Polanco, I, López-Nevot, M-A, Ortega, E, Sierra, E, Gómez de la Concha, E, Urcelay, E, Martín, J

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Polymorphisms in chromosome region 12q13 and their influence on age at onset of type 1 diabetes von Espino-Paisan, L., de la Calle, H., Fernández-Arquero, M., Figueredo, M. Á., de la Concha, E. G., Urcelay, E., Santiago, J. L.

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Epistatic interaction between FCRL3 and NFκB1 genes in Spanish patients with rheumatoid arthritis von Martínez, A, Sánchez, E, Valdivia, A, Orozco, G, López-Nevot, M A, Pascual-Salcedo, D, Balsa, A, Fernández-Gutiérrez, B, de la Concha, E G, García-Sánchez, A, Koeleman, B P C, Urcelay, E, Martín, J

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