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1 ciated with uveitis also are idiopathic (eg, juvenile idiopathic arthritis).
2 tones risk; and between immunoglobulin A and juvenile idiopathic arthritis).
3  been made in the measurement of outcomes in juvenile idiopathic arthritis.
4 t rheumatoid arthritis might have utility in juvenile idiopathic arthritis.
5 idity and mortality seen with systemic onset juvenile idiopathic arthritis.
6 redominantly in children with systemic onset juvenile idiopathic arthritis.
7 ry outcome measures in therapeutic trials in juvenile idiopathic arthritis.
8 ic arthritis (SoJIA) represents up to 20% of juvenile idiopathic arthritis.
9 diopathic uveitis or uveitis associated with juvenile idiopathic arthritis.
10 ophage activation syndrome in systemic onset juvenile idiopathic arthritis.
11 isk of lower respiratory tract infection and juvenile idiopathic arthritis.
12 omandibular joint arthritis in children with juvenile idiopathic arthritis.
13  11 years, range 4-16), of whom 37 (74%) had juvenile idiopathic arthritis.
14 edict temporomandibular joint involvement in juvenile idiopathic arthritis.
15 f S100A12 correlate with disease activity in juvenile idiopathic arthritis.
16 2001on the matter of uveitis associated with juvenile idiopathic arthritis.
17 as been used to treat children with systemic juvenile idiopathic arthritis.
18 he interleukin-1 signature in systemic onset juvenile idiopathic arthritis.
19 compromise the resolution of inflammation in juvenile idiopathic arthritis.
20 tionally is classified under the umbrella of juvenile idiopathic arthritis.
21 anti-citrullinated protein antibody-positive juvenile idiopathic arthritis.
22 anti-citrullinated protein antibody-positive juvenile idiopathic arthritis.
23  ocular morbidity of uveitis associated with juvenile idiopathic arthritis, aggressive therapies can
24 ackground rate of malignancy associated with juvenile idiopathic arthritis, although the impact of me
25 losing spondylitis, psoriatic arthritis, and juvenile idiopathic arthritis among the inflammatory joi
26 ed with biologic agents for the treatment of juvenile idiopathic arthritis and childhood-onset system
27                             The diagnoses of juvenile idiopathic arthritis and childhood-onset system
28 recognized in children and young adults with juvenile idiopathic arthritis and is multifactorial in o
29 rsity before and after HSCT in patients with juvenile idiopathic arthritis and juvenile dermatomyosit
30 aired in a large proportion of children with juvenile idiopathic arthritis and other rheumatic diseas
31 de has been utilized to treat systemic onset juvenile idiopathic arthritis and related autoinflammato
32 tive diseases, significantly most similar to juvenile idiopathic arthritis and significantly least si
33 ary biliary cirrhosis, rheumatoid arthritis, juvenile idiopathic arthritis, and alopecia areata.
34 itions, and preliminary quality measures for juvenile idiopathic arthritis, and cites examples of qua
35 hildhood-onset systemic lupus erythematosus, juvenile idiopathic arthritis, and juvenile dermatomyosi
36 hildhood-onset systemic lupus erythematosus, juvenile idiopathic arthritis, and juvenile dermatomyosi
37      60% were female, approximately half had juvenile idiopathic arthritis, and most were treated wit
38 ty of life in large cohorts of children with juvenile idiopathic arthritis are important in guiding i
39 tic reports of the use of bisphosphonates in juvenile idiopathic arthritis are welcome additions to t
40 re rheumatic diseases, most notably systemic juvenile idiopathic arthritis, are at risk for MAS.
41 ase pathogenesis of lupus and systemic onset juvenile idiopathic arthritis as well as related conditi
42 ctors, and course of ocular hypotony (OH) in juvenile idiopathic arthritis-associated uveitis (JIAU).
43 ses were birdshot chorioretinopathy (n = 3), juvenile idiopathic arthritis-associated uveitis (n = 3)
44 -Hispanic African-American children with non-juvenile idiopathic arthritis-associated uveitis may hav
45                                Many cases of juvenile idiopathic arthritis-associated uveitis, many c
46 setting of certain forms of uveitis, such as juvenile idiopathic arthritis-associated uveitis, remain
47                       As the pathogenesis of juvenile idiopathic arthritis becomes better understood,
48  the incidence of malignancy associated with juvenile idiopathic arthritis, both with and without tre
49 related protein-14 (S100A9) in children with juvenile idiopathic arthritis can indicate clinically oc
50                                              Juvenile idiopathic arthritis continues to provide probl
51                       A 46-year-old man with juvenile idiopathic arthritis developed a pruritic cutan
52 lity of new medications for the treatment of juvenile idiopathic arthritis has made the accurate asse
53 ith rheumatoid factor positive polyarticular juvenile idiopathic arthritis, have the greatest deficit
54                                           In juvenile idiopathic arthritis, heat shock proteins have
55  with seronegative spondyloarthropathies and juvenile idiopathic arthritis; however, etanercept has f
56                  The most common causes were juvenile idiopathic arthritis in 39 patients, pars plani
57 on electrode, aiming at the diagnosis of the juvenile idiopathic arthritis in real serum samples.
58 tumor necrosis factor-alpha inhibitors has a juvenile idiopathic arthritis indication.
59           The armamentarium for treatment of juvenile idiopathic arthritis is expanding at a rapid ra
60 tivity in the development of osteoporosis in juvenile idiopathic arthritis is the focus of several st
61 ), fulfillment of criteria for >1 subtype of juvenile idiopathic arthritis (JIA) (5%), and HLA-B27 in
62  about exercise therapy in the management of juvenile idiopathic arthritis (JIA) along with activity
63 dministered to children and adolescents with juvenile idiopathic arthritis (JIA) and pediatric inflam
64 ination on disease activity in patients with juvenile idiopathic arthritis (JIA) are matters of conce
65                                              Juvenile idiopathic arthritis (JIA) can persist through
66                                              Juvenile idiopathic arthritis (JIA) comprises several cl
67                      Uveitis associated with juvenile idiopathic arthritis (JIA) continues to blind s
68 olyarticular rheumatoid factor (RF)-negative juvenile idiopathic arthritis (JIA) due to the presence
69 loci in oligoarthritis in UK Caucasians with juvenile idiopathic arthritis (JIA) has not been describ
70                       Patients with systemic juvenile idiopathic arthritis (JIA) have arthritis, quot
71                            The chronicity of juvenile idiopathic arthritis (JIA) into adulthood and a
72 ciations for Rheumatology criteria parse out juvenile idiopathic arthritis (JIA) into seven groups, w
73                                              Juvenile idiopathic arthritis (JIA) is a chronic rheumat
74                                              Juvenile idiopathic arthritis (JIA) is a heterogeneous g
75                                              Juvenile idiopathic arthritis (JIA) is a wide group of d
76                                              Juvenile idiopathic arthritis (JIA) is an autoimmune dis
77                                     Systemic juvenile idiopathic arthritis (JIA) is an autoinflammato
78 predict response to therapy in polyarticular juvenile idiopathic arthritis (JIA) is an important issu
79            Assessment of this association in juvenile idiopathic arthritis (JIA) is complicated by ag
80                                     Systemic juvenile idiopathic arthritis (JIA) is frequently associ
81                                              Juvenile Idiopathic Arthritis (JIA) is one of the most c
82                                     Systemic juvenile idiopathic arthritis (JIA) is the most severe s
83                          The pathogenesis of juvenile idiopathic arthritis (JIA) is thought to involv
84                                           In juvenile idiopathic arthritis (JIA) patients, we have pr
85                                              Juvenile idiopathic arthritis (JIA) refers to a collecti
86                          Eight children with juvenile idiopathic arthritis (JIA) served as controls.
87                                  Subtypes of juvenile idiopathic arthritis (JIA) share phenotypic fea
88  concentrations in a cohort of patients with juvenile idiopathic arthritis (JIA) to determine the pre
89 aluations of the well-being of children with juvenile idiopathic arthritis (JIA) typically rely on pa
90 amily in which 9 members were diagnosed with juvenile idiopathic arthritis (JIA) was ascertained.
91 n this work, a novel biosensor for detecting juvenile idiopathic arthritis (JIA) was developed based
92 y reported to be a characteristic feature of juvenile idiopathic arthritis (JIA), but the relevance o
93 chip array to analyze 2,816 individuals with juvenile idiopathic arthritis (JIA), comprising the most
94 in patients with the most common subtypes of juvenile idiopathic arthritis (JIA), IgM rheumatoid fact
95 diseases in the UK population, including RA, juvenile idiopathic arthritis (JIA), psoriasis, psoriati
96 ultifactorial diseases, including autoimmune juvenile idiopathic arthritis (JIA), result from a compl
97                                           In juvenile idiopathic arthritis (JIA), there are now more
98 S on children with the polyarticular form of juvenile idiopathic arthritis (JIA), using 2 independent
99 association study of Caucasian patients with juvenile idiopathic arthritis (JIA), we have previously
100 t evidence from the literature pertaining to juvenile idiopathic arthritis (JIA)-associated uveitis.
101 ciation between cow's milk allergy (CMA) and juvenile idiopathic arthritis (JIA).
102 e gene that causes diastrophic dysplasia, in juvenile idiopathic arthritis (JIA).
103 e and are associated with innate immunity in juvenile idiopathic arthritis (JIA).
104 ge activation syndrome complicating systemic juvenile idiopathic arthritis (JIA).
105 RhMDT) assessment for children with incident juvenile idiopathic arthritis (JIA).
106 h the fever and disease activity of systemic juvenile idiopathic arthritis (JIA).
107 umatoid arthritis (RA), and 19 subjects with juvenile idiopathic arthritis (JIA).
108 ears further defining the pathophysiology of juvenile idiopathic arthritis (JIA).
109 1 is pivotal in the pathogenesis of systemic juvenile idiopathic arthritis (JIA).
110 ociated with a rare group of diseases called juvenile idiopathic arthritis (JIA).
111 and autoantigen in a subset of children with juvenile idiopathic arthritis (JIA).
112 l antibody, is effective in the treatment of juvenile idiopathic arthritis (JIA).
113 trated that there is familial aggregation of juvenile idiopathic arthritis (JIA).
114 ate (MTX) are unpredictable in patients with juvenile idiopathic arthritis (JIA).
115 and autoantigen in a subset of children with juvenile idiopathic arthritis (JIA).
116  is abundant in the synovia of patients with juvenile idiopathic arthritis (JIA).
117 is (RA) and other rheumatic diseases such as juvenile idiopathic arthritis (JIA).
118 il activation in children with polyarticular juvenile idiopathic arthritis (JIA).
119 MTX) in children with selected categories of juvenile idiopathic arthritis (JIA).
120 thin the IL2RA/CD25 gene are associated with juvenile idiopathic arthritis (JIA).
121                      Systemic diagnoses with juvenile idiopathic arthritis (JIA; adjusted hazard rati
122  associated with increased risk for systemic juvenile idiopathic arthritis, leprosy and Crohn's disea
123 in weight-bearing cartilage in patients with juvenile idiopathic arthritis may help with early detect
124 approved dosage for rheumatoid arthritis and juvenile idiopathic arthritis, may be an effective treat
125 tients with uveitic glaucoma associated with juvenile idiopathic arthritis (n = 20), idiopathic uveit
126 NK cells isolated from the synovial fluid of juvenile idiopathic arthritis patients failed to inhibit
127 ophage activation syndrome in systemic onset juvenile idiopathic arthritis patients.
128 ed muscle mass and abnormal bone geometry in juvenile idiopathic arthritis patients.
129 +) monocytes exposed to plasma from systemic juvenile idiopathic arthritis patients.
130 (SF) from patients with osteoarthritis (OA), juvenile idiopathic arthritis, psoriatic arthritis (PsA)
131                The majority of patients with juvenile idiopathic arthritis-related uveitic glaucoma r
132 re was achieved in the eyes of patients with juvenile idiopathic arthritis-related uveitis glaucoma w
133 ing of the risk factors for poor outcomes in juvenile idiopathic arthritis-related uveitis.
134 e far more costly than that of adult SLE and juvenile idiopathic arthritis reported in the literature
135 eitis in children are highlighted, including juvenile idiopathic arthritis, sarcoidosis and Behcet's
136 ned from the synovial fluid of patients with juvenile idiopathic arthritis show marked downregulation
137 rs most frequently in patients with systemic juvenile idiopathic arthritis (SJIA) and systemic lupus
138                                     Systemic juvenile idiopathic arthritis (SJIA) is an inflammatory
139                     When applied to systemic juvenile idiopathic arthritis (sJIA), an autoinflammator
140 escent from the United Kingdom with systemic juvenile idiopathic arthritis (sJIA), with the GG genoty
141 his review summarizes biomarkers in systemic juvenile idiopathic arthritis (sJIA).
142 y, is most strongly associated with systemic juvenile idiopathic arthritis (SJIA).
143                               Systemic onset juvenile idiopathic arthritis (SoJIA) encompasses approx
144                               Systemic onset juvenile idiopathic arthritis (SoJIA) represents up to 2
145 ation is now also reported in systemic onset juvenile idiopathic arthritis (SoJIA).
146 pivotal trial of infliximab in polyarticular juvenile idiopathic arthritis suggested efficacy, but th
147 osed rheumatic diseases in children, such as juvenile idiopathic arthritis, systemic lupus erythemato
148                   The disorders reviewed are juvenile idiopathic arthritis, systemic lupus erythemato
149  in treating chronic uveitis associated with juvenile idiopathic arthritis than etanercept.
150 more frequent manifestation in patients with juvenile idiopathic arthritis than previously believed,
151            In the inflammatory site in human juvenile idiopathic arthritis, the CD39(+)Foxp3(-) popul
152 charged with developing quality measures for juvenile idiopathic arthritis; thus, there is a commitme
153 iments, the addition of NGF to LPS-activated juvenile idiopathic arthritis to both mononuclear cells
154 ortant; no child should be labeled as having juvenile idiopathic arthritis unless there is a clear hi
155 ciated at the inflamed site in patients with juvenile idiopathic arthritis, which led us to question
156                             In patients with juvenile idiopathic arthritis who do not respond to oral
157 ic illness and rheumatic conditions, such as juvenile idiopathic arthritis, who demonstrated no socia

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