Detalles de la búsqueda
1.
Genetic variants within the TNFRSF1B gene and susceptibility to rheumatoid arthritis and response to anti-TNF drugs: a multicenter study.
Pharmacogenet Genomics
; 25(7): 323-33, 2015 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-25850964
2.
Allelic variants in TLR10 gene may influence bilateral affectation and clinical course of Meniere's disease.
Immunogenetics
; 65(5): 345-55, 2013 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-23370977
3.
Functional variants of MIF, INFG and TFNA genes are not associated with disease susceptibility or hearing loss progression in patients with Ménière's disease.
Eur Arch Otorhinolaryngol
; 270(4): 1521-9, 2013 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-23179933
4.
Human adipose tissue as a major reservoir of cytomegalovirus-reactive T cells.
Front Immunol
; 14: 1303724, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-38053998
5.
Reduction of false-negative papillary thyroid carcinomas by the routine analysis of BRAF(T1799A) mutation on fine-needle aspiration biopsy specimens: a prospective study of 814 thyroid FNAB patients.
Ann Surg
; 255(5): 986-92, 2012 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-22504197
6.
Analysis of Class II human leucocyte antigens in Italian and Spanish systemic sclerosis.
Rheumatology (Oxford)
; 51(1): 52-9, 2012 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-22087014
7.
Identification of a new putative functional IL18 gene variant through an association study in systemic lupus erythematosus.
Hum Mol Genet
; 18(19): 3739-48, 2009 Oct 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-19584085
8.
Polymorphisms of CD16A and CD32 Fcγ receptors and circulating immune complexes in Ménière's disease: a case-control study.
BMC Med Genet
; 12: 2, 2011 Jan 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-21208440
9.
Protection against anti-citrullinated protein antibody-positive rheumatoid arthritis is predominantly associated with HLA-DRB1*1301: a meta-analysis of HLA-DRB1 associations with anti-citrullinated protein antibody-positive and anti-citrullinated protein antibody-negative rheumatoid arthritis in four European populations.
Arthritis Rheum
; 62(5): 1236-45, 2010 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-20131291
10.
Novel association of the interleukin 2-interleukin 21 region with inflammatory bowel disease.
Am J Gastroenterol
; 104(8): 1968-75, 2009 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-19471255
11.
Replication of an association between IL23R gene polymorphism with inflammatory bowel disease.
Clin Gastroenterol Hepatol
; 5(8): 977-81, 981.e1-2, 2007 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-17678845
12.
CD209 in inflammatory bowel disease: a case-control study in the Spanish population.
BMC Med Genet
; 8: 75, 2007 Dec 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-18070336
13.
MYO9B gene polymorphisms are associated with autoimmune diseases in Spanish population.
Hum Immunol
; 68(7): 610-5, 2007 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-17584584
14.
HLA-DRB1*1101 allele may be associated with bilateral Méniére's disease in southern European population.
Otol Neurotol
; 28(7): 891-5, 2007 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-17592398
15.
Interleukin 12 (IL12B) and interleukin 12 receptor (IL12RB1) gene polymorphisms in rheumatoid arthritis.
Hum Immunol
; 66(6): 710-5, 2005 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-15993716
16.
Analysis of a GT microsatellite in the promoter of the foxp3/scurfin gene in autoimmune diseases.
Hum Immunol
; 66(8): 869-73, 2005 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-16216670
17.
Analysis of a functional BTNL2 polymorphism in type 1 diabetes, rheumatoid arthritis, and systemic lupus erythematosus.
Hum Immunol
; 66(12): 1235-41, 2005 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-16690410
18.
A functional polymorphism of the NFKB1 promoter is not associated with ulcerative colitis in a Spanish population.
Inflamm Bowel Dis
; 11(6): 576-9, 2005 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-15905705
19.
Human leukocyte antigen-DQB1 and -DRB1 associations in patients with idiopathic sudden sensorineural hearing loss from a defined population of Northwest Spain.
Acta Otolaryngol
; 125(12): 1277-82, 2005 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-16303674
20.
Absence of COCH mutations in patients with Meniere disease.
Eur J Hum Genet
; 12(1): 75-8, 2004 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-14704763