Detalhe da pesquisa
1.
Variants in autoinflammatory diseases-related genes in a family with cold-induced autoinflammatory syndrome.
Clin Exp Rheumatol
; 40(8): 1510-1516, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-35383566
2.
PTPN22 is not associated with Behçet's disease. Study spanning the complete gene region in the Spanish population and meta-analysis of the functional variant R620W.
Clin Exp Rheumatol
; 34(6 Suppl 102): S41-S45, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27050764
3.
Association of CCR5Δ32 and Behçet's disease: new data from a case-control study in the Spanish population and meta-analysis.
Clin Exp Rheumatol
; 33(6 Suppl 94): S96-100, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26393284
4.
Association of haplotypes of the TLR8 locus with susceptibility to Crohn's and Behçet's diseases.
Clin Exp Rheumatol
; 33(6 Suppl 94): S117-22, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26486764
5.
Lack of association of TNFAIP3 and JAK1 with Behçet's disease in the European population.
Clin Exp Rheumatol
; 33(6 Suppl 94): S36-9, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26005883
6.
The complex HLA-E-nonapeptide in Behçet disease.
Front Immunol
; 14: 1080047, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37638008
7.
Monitoring of kinetics and exhaustion markers of circulating CAR-T cells as early predictive factors in patients with B-cell malignancies.
Front Immunol
; 14: 1152498, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37122702
8.
Expression of CD81, SR-BI and LDLR in lymphocytes and monocytes from patients with classic and occult hepatitis C virus infection.
J Med Virol
; 84(11): 1727-36, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22997075
9.
Protein and functional isoform levels and genetic variants of the BAFF and APRIL pathway components in systemic lupus erythematosus.
Sci Rep
; 12(1): 11219, 2022 07 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35780200
10.
Interleukin-28B genetic variants and hepatitis virus infection by different viral genotypes.
Hepatology
; 52(1): 33-7, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20578254
11.
Identification of HAVCR1 gene haplotypes associated with mRNA expression levels and susceptibility to autoimmune diseases.
Hum Genet
; 128(2): 221-9, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20549518
12.
Dose adjustment of clopidogrel in hyper-responder patients with unruptured intracranial aneurysms treated with stents.
J Neurointerv Surg
; 12(5): 499-504, 2020 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-31653753
13.
GIMAP and Behçet disease: no association in the European population.
Ann Rheum Dis
; 73(7): 1433-4, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24625627
14.
Association of Functional Polymorphisms of KIR3DL1/DS1 With Behçet's Disease.
Front Immunol
; 10: 2755, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31849952
15.
Behçet's disease and genetic interactions between HLA-B*51 and variants in genes of autoinflammatory syndromes.
Sci Rep
; 9(1): 2777, 2019 02 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-30808881
16.
Genetic variations in the TLR3 locus are associated with eosinophilic esophagitis.
United European Gastroenterol J
; 6(3): 349-357, 2018 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-29774148
17.
Mutational profile of rare variants in inflammasome-related genes in Behçet disease: A Next Generation Sequencing approach.
Sci Rep
; 7(1): 8453, 2017 08 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-28814775
18.
Genetic Analysis with the Immunochip Platform in Behçet Disease. Identification of Residues Associated in the HLA Class I Region and New Susceptibility Loci.
PLoS One
; 11(8): e0161305, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27548383
19.
The spectrum of mutations in Southern Spanish patients with hemophilia A and identification of 28 novel mutations.
Haematologica
; 90(5): 707-10, 2005 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-15921397
20.
APC germ-line mutations in southern Spanish patients with familial adenomatous polyposis: genotype-phenotype correlations and identification of eight novel mutations.
Genet Test
; 9(1): 37-40, 2005.
Artigo
em Inglês
| MEDLINE | ID: mdl-15857185