Dynamics of plasma cytokines in a patient with deficiency of interleukin‐36 receptor antagonist successfully treated with anakinra
Podlipnik, S., Morgado‐Carrasco, D., Fustà‐Novell, X., Mensa‐Vilaró, A., Arostegui, J.I., Alsina‐Gibert, M., Mascaró Jr, J.M.
Published in British journal of dermatology (1951) (01.04.2018)
Published in British journal of dermatology (1951) (01.04.2018)
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Blau syndrome: cross-sectional data from a multicentre study of clinical, radiological and functional outcomes
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
Published in Rheumatology (Oxford, England) (01.06.2015)
Published in Rheumatology (Oxford, England) (01.06.2015)
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First Egyptian patient with STING-associated vasculopathy with onset in infancy
Shoman, W, El Chazli, Y, ElSawy, I, Aróstegui, JI
Published in Scandinavian journal of rheumatology (04.07.2019)
Published in Scandinavian journal of rheumatology (04.07.2019)
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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
Coto‐Segura, P., Mallo‐Garcia, S., Costa‐Romero, M., Arostegui, J.I., Yague, J., Ramos‐Polo, E., Santos‐Juanes, J.
Published in British journal of dermatology (1951) (01.12.2007)
Published in British journal of dermatology (1951) (01.12.2007)
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Combined type‐1 plasminogen activator inhibitor and NOD2/CARD15 genotyping predicts complicated Crohn's disease behaviour
ALVAREZ‐LOBOS, M., AROSTEGUI, J. I., SANS, M., TASSIES, D., PIU, J., REVERTER, J. C., PIQUE, J. M., YAGÜE, J., PANÉS, J.
Published in Alimentary pharmacology & therapeutics (01.02.2007)
Published in Alimentary pharmacology & therapeutics (01.02.2007)
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Familial CD8 deficiency due to a mutation in the CD8 alpha gene
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
Published in The Journal of clinical investigation (01.07.2001)
Published in The Journal of clinical investigation (01.07.2001)
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Possible association between NOD2 variants and joint surgery in psoriatic arthritis
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
Published in Clinical and experimental rheumatology (2010)
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Published in Clinical and experimental rheumatology (2010)
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Vibratory urticaria–angioedema: further insights into the response patterns to vortex provocation test
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.
Published in Journal of the European Academy of Dermatology and Venereology (01.11.2020)
Published in Journal of the European Academy of Dermatology and Venereology (01.11.2020)
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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
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.
Published in Journal of the European Academy of Dermatology and Venereology (01.12.2019)
Published in Journal of the European Academy of Dermatology and Venereology (01.12.2019)
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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
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
Published in Pediatric rheumatology online journal (28.09.2015)
Published in Pediatric rheumatology online journal (28.09.2015)
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Description of a case of late-onset cryopyrin-associated periodic syndrome due to low-level somatic NLRP3 mosaicism
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
Published in Pediatric rheumatology online journal (28.09.2015)
Published in Pediatric rheumatology online journal (28.09.2015)
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NOD2 mosaicism in Blau syndrome
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
Published in Pediatric rheumatology online journal (28.09.2015)
Published in Pediatric rheumatology online journal (28.09.2015)
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Clinical and genetic features of Spanish patients with Mevalonate kinase deficiency
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
Published in Pediatric rheumatology online journal (28.09.2015)
Published in Pediatric rheumatology online journal (28.09.2015)
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AB0002 Analysis of nlrp3 and nod2 genes in adult onset still’s disease
Garcia-Melchor, E., Grados, D., González-Roca, E., Riera, E., Juan, M., Yagüe, J., Arostegui, J. I., Narváez, J., Olivé, A.
Published in Annals of the rheumatic diseases (01.06.2013)
Published in Annals of the rheumatic diseases (01.06.2013)
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THU0479 Biological Therapy for Autoinflammatory Disorders: Single Center Experience in Adult Patients
Bujan Rivas, S., Arostegui, J. I., Martinez Valle, F., Solans Laque, R., Andres Cordon, J. F., Ordi Ros, J., Vilardell Tarres, M.
Published in Annals of the rheumatic diseases (01.06.2013)
Published in Annals of the rheumatic diseases (01.06.2013)
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[Translated article] Schnitzler Syndrome, and the MEFV Gene Variant
Nicolás-Sánchez, F.J., Aróstegui-Gorospe, J.I., Tarragona-Foradada, J., González-Barranquero, A.
Published in Actas dermo-sifiliográficas (01.07.2024)
Published in Actas dermo-sifiliográficas (01.07.2024)
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Copy number variation in the CCL4L gene is associated with susceptibility to acute rejection in lung transplantation
Colobran, R, Casamitjana, N, Roman, A, Faner, R, Pedrosa, E, Arostegui, J I, Pujol-Borrell, R, Juan, M, Palou, E
Published in Genes and immunity (01.04.2009)
Published in Genes and immunity (01.04.2009)
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Severe congenital neutropenia: analysis of clinical features, diagnostic methods, treatment and long-term outcome
Milá, M, Rufach, A, Dapena, J L, Arostegui, J I, Elorza, I, Llort, A, Sánchez de Toledo, J, Díaz de Heredia, C
Published in Anales de pediatría (Barcelona, Spain : 2003) (01.12.2011)
Published in Anales de pediatría (Barcelona, Spain : 2003) (01.12.2011)
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Development of a workflow to analyze autoinflammatory-associated genes using AccessArray™ system and next generation sequencing
Gonzalez-Roca, E, Ruiz-Ortiz, E, Anton, MC, Plaza, S, Mensa-Vilaro, A, Yagüe, J, Arostegui, JI
Published in Pediatric rheumatology online journal (28.09.2015)
Published in Pediatric rheumatology online journal (28.09.2015)
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