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Page 1
Unexpected relevant role of gene mosaicism in patients with primary immunodeficiency diseases.
Mensa-Vilaró A, Bravo García-Morato M, de la Calle-Martin O, Franco-Jarava C, Martínez-Saavedra MT, González-Granado LI, González-Roca E, Fuster JL, Alsina L, Mutchinick OM, Balderrama-Rodríguez A, Ramos E, Modesto C, Mesa-Del-Castillo P, Ortego-Centeno N, Clemente D, Souto A, Palmou N, Remesal A, Leslie KS, Gómez de la Fuente E, Yadira Bravo Gallego L, Campistol JM, Dhouib NG, Bejaoui M, Dutra LA, Terreri MT, Mosquera C, González T, Cañellas J, García-Ruiz de Morales JM, Wouters CH, Bosque MT, Cham WT, Jiménez-Treviño S, de Inocencio J, Bloomfield M, Pérez de Diego R, Martínez-Pomar N, Rodríguez-Pena R, González-Santesteban C, Soler-Palacín P, Casals F, Yagüe J, Allende LM, Rodríguez-Gallego JC, Colobran R, Martínez-Martínez L, López-Granados E, Aróstegui JI. Mensa-Vilaró A, et al. Among authors: arostegui ji. J Allergy Clin Immunol. 2019 Jan;143(1):359-368. doi: 10.1016/j.jaci.2018.09.009. Epub 2018 Sep 29. J Allergy Clin Immunol. 2019. PMID: 30273710 Free article. Clinical Trial.
Familial CD8 deficiency due to a mutation in the CD8 alpha gene.
de la Calle-Martin O, Hernandez M, Ordi J, Casamitjana N, Arostegui JI, Caragol I, Ferrando M, Labrador M, Rodriguez-Sanchez JL, Espanol T. de la Calle-Martin O, et al. Among authors: arostegui ji. J Clin Invest. 2001 Jul;108(1):117-23. doi: 10.1172/JCI10993. J Clin Invest. 2001. PMID: 11435463 Free PMC article.
A severe autosomal-dominant periodic inflammatory disorder with renal AA amyloidosis and colchicine resistance associated to the MEFV H478Y variant in a Spanish kindred: an unusual familial Mediterranean fever phenotype or another MEFV-associated periodic inflammatory disorder?
Aldea A, Campistol JM, Arostegui JI, Rius J, Maso M, Vives J, Yagüe J. Aldea A, et al. Among authors: arostegui ji. Am J Med Genet A. 2004 Jan 1;124A(1):67-73. doi: 10.1002/ajmg.a.20296. Am J Med Genet A. 2004. PMID: 14679589
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: arostegui ji. Ann Surg. 2005 Nov;242(5):693-700. doi: 10.1097/01.sla.0000186173.14696.ea. Ann Surg. 2005. PMID: 16244543 Free PMC article.
Association of intermittent hydrarthrosis with MEFV gene mutations.
Cañete JD, Aróstegui JI, Queiró R, Sanmartí R, Ballina J, Bosch X, Yagüe J. Cañete JD, et al. Among authors: arostegui ji. Arthritis Rheum. 2006 Jul;54(7):2334-5. doi: 10.1002/art.21923. Arthritis Rheum. 2006. PMID: 16802374 Free article. No abstract available.
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. Arthritis Rheum. 2007 Nov;56(11):3805-13. doi: 10.1002/art.22966. Arthritis Rheum. 2007. PMID: 17968944 Free article.
169 results