Severe Raynaud syndrome induced by adjuvant interferon alfa in metastatic melanoma

Por Husein–ElAhmed, H., Callejas–Rubio, J.L., Olmo, R. Ortega Del, Ríos–Fernandez, R., Ortego–Centeno, N.
Publicado em 2010

Study of the role of functional variants of SLC22A4, RUNX1 and SUMO4 in systemic lupus erythematosus

Por Orozco, G, Sánchez, E, Gómez, L M, González‐Gay, M A, López‐Nevot, M A, Torres, B, Ortego‐Centeno, N, Jiménez‐Alonso, J, de Ramón, E, Román, J Sánchez, Anaya, J M, Sturfelt, G, Gunnarsson, I, Svennungsson, E, Alarcón‐Riquelme, M, González‐Escribano, M F, Martín, J
Publicado em 2006

Polymorphisms in the interleukin 4, interleukin 13 and corresponding receptor genes are not associated with Systemic Sclerosis and do not influence gene expression

Por Broen, JCA, Dieude, P, Vonk, M C, Beretta, L, Rueda, B, Herrick, A, Worthington, J, Hunzelmann, N, Riemekasten, G, Kiener, H, Scorza, R, Simeon, C P, Fonollosa, V, Carreira, P, Ortego-Centeno, N, Gonzalez-Gay, M A, Airò, P, Coenen, MJH, Aliprantis, A, Martin, J, Allanore, Y, Radstake, TRDJ
Publicado em 2010

A large multicenter analysis of CTGF -945 promoter polymorphism does not confirm association with Systemic Sclerosis susceptibility or phenotype

Por Rueda, B, Simeon, C, Hesselstrand, R, Herrick, A, Worthington, J, Ortego-Centeno, N, Riemekasten, G, Fonollosa, V, Vonk, MC, van den Hoogen, FHJ, Sanchez-Román, J, Aguirre-Zamorano, MA, García-Portales, R, Pros, A, Camps, MT, Gonzalez-Gay, MA, Gonzalez-Escribano, MF, Coenen, MJ, Lambert, N, Nelson, JL, Radstake, TRDJ, Martin, J.
Publicado em 2008

Variants of PBEF predispose to systemic sclerosis and pulmonary arterial hypertension development

Por Broen, JCA, Gourh, P, Vonk, M C, Beretta, L, Niederer, F, Rueda, B, Geurts-van Bon, L, Brouwer, C, Hesselstrand, R, Herrick, A, Worthington, J, Hunzelman, N, Denton, C, Fonseca, C, Riemekasten, G, Kiener, H, Scorza, R, Simeon, C P, Fonollosa, V, Carreira, P, Ortego-Centeno, N, Gonzalez-Gay, M A, Airò, P, Coenen, MJH, Mayes, M, Kyburz, D, Arnett, F C, Martin, J, Radstake, TRDJ
Publicado em 2010

Identification of the PTPN22 functional variant R620W as susceptibility genetic factor for giant cell arteritis

Por Serrano, A, Márquez, A, Mackie, SL, Carmona, FD, Solans, R, Miranda-Filloy, JA, Hernández-Rodríguez, J, Cid, MC, Castañeda, S, Morado, IC, Narváez, J, Blanco, R, Sopeña, B, García-Villanueva, MJ, Monfort, J, Ortego-Centeno, N, Unzurrunzaga, A, Marí-Alfonso, B, Sánchez Martín, J, de Miguel, E, Magro, C, Raya, E, Braun, N, Latus, J, Molberg, O, Lie, BA, Moosig, F, Witte, T, Morgan, AW, González-Gay, MA, Martín, J
Publicado em 2013

BANK1 functional variants are associated with susceptibility to diffuse systemic sclerosis in Caucasians

Por Rueda, B, Gourh, P, Broen, J, Agarwal, S K, Simeon, C, Ortego-Centeno, N, Vonk, M C, Coenen, M, Riemekasten, G, Hunzelmann, N, Hesselstrand, R, Tan, F K, Reveille, J D, Assassi, S, Garcia-Hernandez, F J, Carreira, P, Camps, M, Fernandez-Nebro, A, de la Peña, P Garcia, Nearney, T, Hilda, D, Gónzalez-Gay, M A, Airo, P, Beretta, L, Scorza, R, Radstake, T R D J, Mayes, M D, Arnett, F C, Martin, J
Publicado em 2009

Analysis of the influence of PTPN22 gene polymorphisms in systemic sclerosis

Por Diaz-Gallo, LM, Gourh, P, Broen, J, Simeon, C, Fonollosa, V, Ortego-Centeno, N, Agarwal, S, Vonk, MC, Coenen, M, Riemekasten, G, Hunzelmann, N, Hesselstrand, R, Tan, FK, Reveille, JD, Assassi, S, García-Hernandez, FJ, Carreira, P, Camps, MT, Fernandez-Nebro, A, de la Peña, P Garcia, Nearney, T, Hilda, D, González-Gay, MA, Airo, P, Beretta, L, Scorza, R, Herrick, A, Worthington, J, Pros, A, Gómez-Gracia, I, Trapiella, L, Espinosa, G, Castellvi, I, Witte, T, de Keyser, F, Vanthuyne, M, Mayes, MD, Radstake, TRDJ, Arnett, FC, Martin, J, Rueda, B
Publicado em 2010

Registry of the Spanish Network for Systemic Sclerosis: Survival, Prognostic Factors, and Causes of Death

Por Simeón-Aznar, C.P., Fonollosa-Plá, V., Tolosa-Vilella, Carles, Espinosa-Garriga, G., Campillo-Grau, M., Ramos-Casals, M., García-Hernández, F.J., Castillo-Palma, M.J., Sánchez-Román, J., Callejas-Rubio, J.L., Ortego-Centeno, N., Egurbide-Arberas, M.V., Trapiellla-Martínez, L., Caminal-Montero, L., Sáez-Comet, L., Velilla-Marco, J., Camps-García, M.T., de Ramón-Garrido, E., Esteban-Marcos, E.M., Pallarés-Ferreres, L., Navarrete-Navarrete, N., Vargas-Hitos, J.A., de la Torre, R. Gómez, Salvador-Cervello, G., Rios-Blanco, J.J., Vilardell-Tarrés, M.
Publicado no Medicine (Baltimore) (2015)

A replication study confirms the association of TNFSF4 (OX40L) polymorphisms with Systemic Sclerosis in a large European cohort

Por Airó P, Lie B A, Palm Ø, Nordin A, Padykov L, Claes K, Denton C, Fonseca C, Madhok R, Shiels P, Chee M M, Schuerwegh A J, Voskuyl A E, De Langhe E, Westhovens R, Smith V, De Keyser F, Houssiau F, Koeleman B P, Coenen MJH, Witte T, Riemekasten G, Hesselstrand R, González-Gay M A, Pros A, García de la Peña P, Follonosa V, Egurbide M V, Fernández-Nebro A, Gallego M, Castellví I, García-Hernández F J, Gómez-Gracia I, Román-Ivorra J A, Tolosa C, Rodríguez L, Vicente-Rabaneda E, González-Escribano M F, Navarrete N, Camps M T, Carreira P, Espinosa G, Ortego-Centeno N, Vonk M C, Beretta L, Simeon C P, Broen JCA, Bossini-Castillo L, Scorza R, van Laar J M, Hunzelmann N, Kreuter A, Herrick A, Worthington J, Radstake TRDJ, Martín J, Rueda B
Publicado em 2010-11-01

A replication study confirms the association of TNFSF4 (OX40L) polymorphisms with Systemic Sclerosis in a large European cohort

Por Bossini-Castillo, L, Broen, JCA, Simeon, C P, Beretta, L, Vonk, M C, Ortego-Centeno, N, Espinosa, G, Carreira, P, Camps, M T, Navarrete, N, González-Escribano, M F, Vicente-Rabaneda, E, Rodríguez, L, Tolosa, C, Román-Ivorra, J A, Gómez-Gracia, I, García-Hernández, F J, Castellví, I, Gallego, M, Fernández-Nebro, A, Egurbide, M V, Follonosa, V, García de la Peña, P, Pros, A, González-Gay, M A, Hesselstrand, R, Riemekasten, G, Witte, T, Coenen, MJH, Koeleman, B P, Houssiau, F, Smith, V, De Keyser, F, Westhovens, R, De Langhe, E, Voskuyl, A E, Schuerwegh, A J, Chee, M M, Madhok, R, Shiels, P, Fonseca, C, Denton, C, Claes, K, Padykov, L, Nordin, A, Palm, Ø, Lie, B A, Airó, P, Scorza, R, van Laar, J M, Hunzelmann, N, Kreuter, A, Herrick, A, Worthington, J, Radstake, TRDJ, Martín, J, Rueda, B
Publicado em 2010

Identification of novel genetic markers associated with the clinical phenotypes of systemic sclerosis through a genome wide association strategy

Por Gorlova, O, Martin, J M, Rueda, B, Koeleman, BPC, Ying, J, Teruel, M, Diaz-Gallo, L M, Broen, J C, Vonk, M C, Simeon, C P, Alizadeh, B Z, Coenen, MJH, Voskuyl, A E, Schuerwegh, A J, van Riel, PLCM, Vanthuyne, M, van ‘t Slot, R, Italiaander, A, Ophoff, R A, Hunzelmann, N, Fonollosa, V, Ortego-Centeno, N, González-Gay, M A, García-Hernández, F J, González-Escribano, M F, Airo, P, van Laar, J, Worthington, J, Hesselstrand, R, Smith, V, De Keyser, F, Houssiau, F, Chee, M M, Madhok, R, Shiels, P, Westhovens, R, Kreuter, A, de Baere, E, Witte, T, Padyukov, L, Nordin, A, Scorza, R, Lunardi, C, Lie, B A, Hoffmann-Vold, A M, García de la Peña, P, Carreira, P, Varga, J, Hinchcliff, M, Lee, A T, Gourh, P, Amos, C I, Riemekasten, G, Herrick, A, Beretta, L, Fonseca, C, Denton, C P, Gregersen, P K, Agarwal, S, Assassi, S, Tan, F K, Arnett, F C, Radstake, TRDJ, Mayes, M D, Martin, J
Publicado em 2010