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Page 1
NOD2 gene-associated pediatric granulomatous arthritis: clinical diversity, novel and recurrent mutations, and evidence of clinical improvement with interleukin-1 blockade in a Spanish cohort.
Aróstegui JI, Arnal C, Merino R, Modesto C, Antonia Carballo M, Moreno P, García-Consuegra J, Naranjo A, Ramos E, de Paz P, Rius J, Plaza S, Yagüe J. Aróstegui JI, et al. Among authors: plaza s. Arthritis Rheum. 2007 Nov;56(11):3805-13. doi: 10.1002/art.22966. Arthritis Rheum. 2007. PMID: 17968944 Free article.
A somatic NLRP3 mutation as a cause of a sporadic case of chronic infantile neurologic, cutaneous, articular syndrome/neonatal-onset multisystem inflammatory disease: Novel evidence of the role of low-level mosaicism as the pathophysiologic mechanism underlying mendelian inherited diseases.
Aróstegui JI, Lopez Saldaña MD, Pascal M, Clemente D, Aymerich M, Balaguer F, Goel A, Fournier del Castillo C, Rius J, Plaza S, López Robledillo JC, Juan M, Ibañez M, Yagüe J. Aróstegui JI, et al. Among authors: plaza s. Arthritis Rheum. 2010 Apr;62(4):1158-66. doi: 10.1002/art.27342. Arthritis Rheum. 2010. PMID: 20131270 Free article.
Etanercept plus colchicine treatment in a child with tumour necrosis factor receptor-associated periodic syndrome abolishes auto-inflammatory episodes without normalising the subclinical acute phase response.
Aróstegui JI, Solís P, Aldea A, Cantero T, Rius J, Bahíllo P, Plaza S, Vives J, Gómez S, Yagüe J. Aróstegui JI, et al. Among authors: plaza s. Eur J Pediatr. 2005 Jan;164(1):13-6. doi: 10.1007/s00431-004-1563-1. Epub 2004 Nov 10. Eur J Pediatr. 2005. PMID: 15549379
Novel evidences of atypical manifestations in cryopyrin-associated periodic syndromes.
Bujan-Rivas S, Basagaña M, Sena F, Méndez M, Dordal MT, Gonzalez-Roca E, Ruiz-Ortiz E, Mensa-Vilaró A, Plaza S, Modesto C, Ordi-Ros J, Yagüe J, Martínez-Valle F, Aróstegui JI. Bujan-Rivas S, et al. Among authors: plaza s. Clin Exp Rheumatol. 2017 Nov-Dec;35 Suppl 108(6):27-31. Epub 2017 Jan 9. Clin Exp Rheumatol. 2017. PMID: 28079503
Crohn's disease patients carrying Nod2/CARD15 gene variants have an increased and early need for first surgery due to stricturing disease and higher rate of surgical recurrence.
Alvarez-Lobos M, Arostegui JI, Sans M, Tassies D, Plaza S, Delgado S, Lacy AM, Pique JM, Yagüe J, Panés J. Alvarez-Lobos M, et al. Among authors: plaza s. Ann Surg. 2005 Nov;242(5):693-700. doi: 10.1097/01.sla.0000186173.14696.ea. Ann Surg. 2005. PMID: 16244543 Free PMC article.
First Description of Late-Onset Autoinflammatory Disease Due to Somatic NLRC4 Mosaicism.
Ionescu D, Peñín-Franch A, Mensa-Vilaró A, Castillo P, Hurtado-Navarro L, Molina-López C, Romero-Chala S, Plaza S, Fabregat V, Buján S, Marques J, Casals F, Yagüe J, Oliva B, Fernández-Pereira LM, Pelegrín P, Aróstegui JI. Ionescu D, et al. Among authors: plaza s. Arthritis Rheumatol. 2022 Apr;74(4):692-699. doi: 10.1002/art.41999. Epub 2022 Feb 14. Arthritis Rheumatol. 2022. PMID: 34672126
209 results