Dynamics of plasma cytokines in a patient with deficiency of interleukin‐36 receptor antagonist successfully treated with anakinra von Podlipnik, S., Morgado‐Carrasco, D., Fustà‐Novell, X., Mensa‐Vilaró, A., Arostegui, J.I., Alsina‐Gibert, M., Mascaró Jr, J.M.

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Blau syndrome: cross-sectional data from a multicentre study of clinical, radiological and functional outcomes von Rosé, Carlos D, Pans, Steven, Casteels, Ingele, Anton, Jordi, Bader-Meunier, Brigitte, Brissaud, Philippe, Cimaz, Roland, Espada, Graciella, Fernandez-Martin, Jorge, Hachulla, Eric, Harjacek, Miroslav, Khubchandani, Raju, Mackensen, Friederike, Merino, Rosa, Naranjo, Antonio, Oliveira-Knupp, Sheila, Pajot, Christine, Russo, Ricardo, Thomée, Caroline, Vastert, Sebastiaan, Wulffraat, Nico, Arostegui, Juan I, Foley, Kevin P, Bertin, John, Wouters, Carine H

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Vibratory urticaria–angioedema: further insights into the response patterns to vortex provocation test von Vergara‐de‐la‐Campa, L., Gatica‐Ortega, M.E., Pastor‐Nieto, M.A., Molina‐Figueras, E., Pérez‐Mesonero, R., Luna‐Bastante, L., Sánchez‐Matas, I., Checa‐Díaz, P., Arostegui, J.I., Giménez‐Arnau, A.

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Expanding the clinical features of autoinflammation and phospholipase Cγ2‐associated antibody deficiency and immune dysregulation by description of a novel patient von Morán‐Villaseñor, E., Saez‐de‐Ocariz, M., Torrelo, A., Arostegui, J.I., Yamazaki‐Nakashimada, M.A., Alcántara‐Ortigoza, M.A., González‐del‐Angel, A., Velázquez‐Aragón, J.A., López‐Herrera, G., Berrón‐Ruiz, L., García‐Romero, M.T.

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A sporadic case of early‐onset sarcoidosis resembling Blau syndrome due to the recurrent R334W missense mutation on the NOD2 gene von Coto‐Segura, P., Mallo‐Garcia, S., Costa‐Romero, M., Arostegui, J.I., Yague, J., Ramos‐Polo, E., Santos‐Juanes, J.

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Familial CD8 deficiency due to a mutation in the CD8 alpha gene von de la Calle-Martin, O, Hernandez, M, Ordi, J, Casamitjana, N, Arostegui, J I, Caragol, I, Ferrando, M, Labrador, M, Rodriguez-Sanchez, J L, Espanol, T

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Combined type‐1 plasminogen activator inhibitor and NOD2/CARD15 genotyping predicts complicated Crohn's disease behaviour von ALVAREZ‐LOBOS, M., AROSTEGUI, J. I., SANS, M., TASSIES, D., PIU, J., REVERTER, J. C., PIQUE, J. M., YAGÜE, J., PANÉS, J.

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A family carrying a homozygous LACC1 truncated mutation expands the clinical phenotype of this disease beyond systemic-onset juvenile idiopathic arthritis von Arostegui, JI, Rabionet, R, Remesal, A, Mensa-Vilaro, A, Murias, S, Alcobendas, R, Gonzalez-Roca, E, Dreschsel, O, Ruiz-Ortiz, E, Puig, A, Comas, D, Ossowski, S, Yagüe, J, Estivill, X, Merino, R

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Possible association between NOD2 variants and joint surgery in psoriatic arthritis von GRAELL, E, AROSTEGUI, J. I, SANMARTI, R, BLANCO, F. J, YAGUE, J, PINTO, J. A, PLAZA, S, FERNANDEZ-SUEIRO, J. L, GONZALEZ, A, CANETE, J. D

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Description of a case of late-onset cryopyrin-associated periodic syndrome due to low-level somatic NLRP3 mosaicism von Mensa-Vilaro, A, Bosque-Peralta, MT, Gonzalez-Roca, E, Casorran-Berges, M, Delgado-Beltran, C, Plaza, S, Anton, MC, Ruiz-Ortiz, E, Yagüe, J, Arostegui, JI

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NOD2 mosaicism in Blau syndrome von Mensa-Vilaro, A, De Inocencio, J, Cham, W Tarng, Gonzalez-Roca, E, Tejada-Palacios, P, Tang, S Ping, Ruiz-Ortiz, E, Enriquez-Merayo, E, Lim, S Chin, Magri, G, Plaza, S, Anton, MC, Cerutti, A, Ariffin, R, Yagüe, J, Arostegui, JI

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Clinical and genetic features of Spanish patients with Mevalonate kinase deficiency von Ruiz-Ortiz, E, Gonzalez-Roca, E, Mensa-Vilaro, A, Rius, J, Plaza, S, Anton, C, Calvo, I, Modesto, C, Anton, J, Arnal, C, Alvarez, C, Alvarez-Coca, J, Becerra, E, Bilbao, N, Camacho, M, Crespo, J, de Diego, C, Diez-Garcia, LF, Espinosa, L, Garcia-Escriva, D, de Gracia, F, Gonzalez, MI, Iglesias, E, Izquierdo, S, Lastra, B, Llobet, P, Lopez, B, Lopez-Gonzalez, V, Martinez, R, Martin-Mateos, MA, Merino, R, Ortega, L, Peiro, ME, de Soto, I Perez, Perez-Mendez, C, Rodriguez-Valverde, V, Ribes, A, Ruiz, A, Sanchez, B, Santos, JL, Sevilla, B, Sotoca, J, Vilas, J, Villoria, A, Yagüe, J, Arostegui, JI

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[Translated article] Schnitzler Syndrome, and the MEFV Gene Variant von Nicolás-Sánchez, F.J., Aróstegui-Gorospe, J.I., Tarragona-Foradada, J., González-Barranquero, A.

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THU0479 Biological Therapy for Autoinflammatory Disorders: Single Center Experience in Adult Patients von Bujan Rivas, S., Arostegui, J. I., Martinez Valle, F., Solans Laque, R., Andres Cordon, J. F., Ordi Ros, J., Vilardell Tarres, M.

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AB0002 Analysis of nlrp3 and nod2 genes in adult onset still’s disease von Garcia-Melchor, E., Grados, D., González-Roca, E., Riera, E., Juan, M., Yagüe, J., Arostegui, J. I., Narváez, J., Olivé, A.

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Positive clinical and biochemical responses to anakinra in a 3-yr-old patient with cryopyrin-associated periodic syndrome (CAPS) von Ramos, E., Aróstegui, J. I., Campuzano, S., Rius, J., Bousoño, C., Yagüe, J.

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Copy number variation in the CCL4L gene is associated with susceptibility to acute rejection in lung transplantation von Colobran, R, Casamitjana, N, Roman, A, Faner, R, Pedrosa, E, Arostegui, J I, Pujol-Borrell, R, Juan, M, Palou, E

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Development of a workflow to analyze autoinflammatory-associated genes using AccessArray™ system and next generation sequencing von Gonzalez-Roca, E, Ruiz-Ortiz, E, Anton, MC, Plaza, S, Mensa-Vilaro, A, Yagüe, J, Arostegui, JI

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Somatic NLRP3 mosaicism in Muckle-Wells syndrome von Gonzalez-Roca, E, Mensa-Vilaro, A, Plaza, S, Anton, MC, Rius, J, Ruiz-Ortiz, E, Campistol, JM, Souto, A, Cañellas, J, Nakagawa, K, Nishikomori, R, Yagüe, J, Arostegui, JI

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THU0480 AA-Amyloidosis as Diagnostic Clue of a Family with Atypical Cryopirin Associated Periodic Syndrome with Muckle-Wells Syndrome Phenotype von Bujan Rivas, S., Arostegui Gorospe, J. I., Sellas Fernandez, A., Simeon Aznar, C. P., Aguilar Company, J., Ordi Ros, J., Vilardell Tarres, M.

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