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1 or the treatment of ocular manifestations of Behcet's disease.
2 eitis, and finally, somewhat controversially Behcet's disease.
3 enic pathways in the spondyloarthritides and Behcet's disease.
4 on in the management of venous thrombosis in Behcet's disease.
5 fied 5 novel genetic susceptibility loci for Behcet's disease.
6 ve emerged as a successful approach to treat Behcet's disease.
7 venile idiopathic arthritis, sarcoidosis and Behcet's disease.
8 d the International Study Group criteria for Behcet's disease.
9 ss in patients with a familial occurrence of Behcet's disease.
10 her characteristic or diagnostic features of Behcet's disease.
11 s disease, systemic lupus erythematosus, and Behcet's disease.
12 iant cell arteritis, Takayasu arteritis, and Behcet's disease.
13              Main causes of uveitis included Behcet's disease (17.2%), birdshot chorioretinopathy (11
14 95% confidence interval [CI], 0.19-0.74) and Behcet's disease (aHR, 0.10; 95% CI, 0.01-0.85) were ass
15  genotypes in 1,209 Turkish individuals with Behcet's disease and 1,278 controls.
16 a number of inflammatory diseases, including Behcet's disease and age-related macular degeneration.
17 lvement of other autoimmune diseases such as behcet's disease and ankylosing spondylitis, and ocular
18 the genetic association between HLA-B*51 and Behcet's disease and exploring additional susceptibility
19  cause monogenic recessive diseases: MEFV in Behcet's disease and Henoch-Schonlein purpura, and A1AT
20 (GWAS) in vasculitis have been published, in Behcet's disease and Kawasaki disease; none of the genes
21 as demonstrated efficacy in the treatment of Behcet's disease and other forms of posterior uveitis.
22 udy is the first systematic genome screen in Behcet's disease and provides evidence of linkage to sev
23  II HLA associations for PFAPA distinct from Behcet's disease and recurrent aphthous stomatitis.
24 wo other oropharyngeal ulcerative disorders, Behcet's disease and recurrent aphthous stomatitis.
25 ious uveitides (the ocular manifestations of Behcet's disease and sarcoidosis) based on multicolor fl
26 mal set of 5 markers that accurately predict Behcet's disease and sarcoidosis.
27              The genetic association between Behcet's disease and UBAC2 was established, replicated,
28  and mortality of large vessel vasculitis in Behcet's disease are improving.
29 lear cells of individuals homozygous for the Behcet's disease-associated "G" allele.
30 nfliximab and interferon alpha, particularly Behcet's disease-associated uveitis.
31 chemokines and its receptor in patients with Behcet's disease (BD) and their associations with diseas
32 ssociated with the autoinflammatory disorder Behcet's disease (BD) in epistasis with HLA-B*51, which
33 ly genes with Vogt-Koyanagi-Harada (VKH) and Behcet's disease (BD) in Han Chinese.
34 matosus (SLE) in subjects from Colombia; and Behcet's disease (BD) in subjects from Turkey.
35                                              Behcet's disease (BD) is a chronic, relapsing, systemic
36                                              Behcet's disease (BD) is a multi-system inflammatory dis
37                                              Behcet's disease (BD) is a multi-systemic inflammatory d
38                                              Behcet's disease (BD) is a multisystem disease of unknow
39                                              Behcet's disease (BD) is a multisystem disorder of unkno
40                                              Behcet's disease (BD) is a multisystem immune-mediated i
41                                              Behcet's disease (BD) is a multisystem relapsing inflamm
42                                              Behcet's disease (BD) is a rare, multisystem inflammator
43                                              Behcet's Disease (BD) is diagnosed as continuing systema
44                                              Behcet's disease (BD) is reportedly associated with poly
45                                              Behcet's disease (BD) manifests as an autoimmune disorde
46                                              Behcet's disease (BD) pathogenesis involves severe outco
47 aging features of myelopathy associated with Behcet's disease (BD).
48 nous retinal detachment (RD) associated with Behcet's disease (BD).
49 lpha) may play a role in the pathogenesis of Behcet's disease (BD).
50 atients (n = 52, F:M = 40:12), patients with Behcet's disease (BD, n = 40, F:M = 29:11) as another sy
51 r uveitis cases included diagnosis with JIA, Behcet's disease, bilateral uveitis, history of cataract
52                    We analyzed 1,900 Turkish Behcet's disease cases and 1,779 controls genotyped with
53  with 311,459 SNPs in 1,215 individuals with Behcet's disease (cases) and 1,278 healthy controls from
54 analysis of 24,834 variants in 2 independent Behcet's disease cohorts from 2 ancestry groups.
55 correlated with disease activity in terms of Behcet's Disease Current Activity Form (BDCAF) (p < 0.00
56 und in the peripheral blood of patients with Behcet's disease during episodes of ocular inflammation.
57 NCA)-associated vasculitis, Crohn's disease, Behcet's disease, eosinophilic granulomatosis with polya
58 between an HLA class I antigen, HLA-B51, and Behcet's disease has long been known.
59 anding knowledge on large vessel problems in Behcet's disease, highlighting recent contributions.
60                        Ocular involvement in Behcet's disease, if untreated, leads to blindness.
61  patients, pars planitis in 16 patients, and Behcet's disease in 13 patients.
62 ed the genetic association between UBAC2 and Behcet's disease in 3 independent sets of patients and c
63 ntification of other susceptibility loci for Behcet's disease in multicase families.
64 etic effects that increase susceptibility to Behcet's disease in the UBAC2 locus.
65       Most published diagnostic criteria for Behcet's disease include the classic triad of orogenital
66                                              Behcet's disease is a genetically complex disease of unk
67                                              Behcet's disease is a multisystem inflammatory disorder
68                                              Behcet's disease is an inflammatory disease characterize
69                          The vasculopathy of Behcet's disease is distinctive among the vasculitides i
70 gest that the robust HLA-B*51 association in Behcet's disease is explained by a variant located betwe
71                                              Behcet's disease is generally considered to be a multifa
72 teristics of ocular disease in children with Behcet's disease is presented.
73                  An article on the course of Behcet's disease is reviewed as well as another article
74 gly, allotype 10, previously associated with Behcet's disease, is consistently a low-activity outlier
75 sic part of familial Mediterranean fever and Behcet's disease management.
76 current aphthous stomatitis on the mild end, Behcet's disease on the severe end, and PFAPA intermedia
77 ared to ankylosing spondylitis (p = 0.0001), behcet's disease (p = 0.0001), presumed latent tuberculo
78 pect to ankylosing spondylitis (p = 0.0001), behcet's disease, (p = 0.0001) presumed latent tuberculo
79                    We studied a total of 676 Behcet's disease patients and 1,096 controls.
80                                    Pediatric Behcet's disease (PBD) is rarer than BD and can be a cha
81 ng recurrent aphthous stomatitis, PFAPA, and Behcet's disease, placing these disorders on a common sp
82 olving patients with ankylosing spondylitis, behcet's disease, presumed sarcoidosis, presumed latent
83                                              Behcet's disease runs a chronic course, with unpredictab
84                             Individuals with Behcet's disease suffer from episodic inflammation often
85 irst step toward the identification of novel Behcet's disease susceptibility genes.
86 ate immune response to microbial exposure in Behcet's disease susceptibility.
87 a patient who had a vasculopathy fitting the Behcet's disease type, but who lacked the other characte
88                                              Behcet's disease typically arises in young adults, altho
89      To discover new susceptibility loci for Behcet's disease, we performed a genome-wide association
90                       The disorder resembles Behcet's disease, which is typically considered a polyge
91 ulitis occurs in a subgroup of patients with Behcet's disease who are at high risk for disease-relate
92        We confirmed the known association of Behcet's disease with HLA-B*51 and identified a second,
93 ave shown an increased rate of thrombosis in Behcet's disease, with a different clinical presentation