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1 n IL-17 inhibitor, in non-radiographic axial spondyloarthritis.
2 ociated with systemic disease, such as axial spondyloarthritis.
3 e currently no diagnostic criteria for axial spondyloarthritis.
4 patients with active non-radiographic axial spondyloarthritis.
5 ty of upadacitinib in non-radiographic axial spondyloarthritis.
6 ts can improve the accuracy for diagnosis of spondyloarthritis.
7 hritides, including rheumatoid arthritis and spondyloarthritis.
8 ment, and patient global assessment in axial spondyloarthritis.
9 tis, but was ineffective in studies of axial spondyloarthritis.
10 n of upadacitinib for the treatment of axial spondyloarthritis.
11 e as targets for therapeutic intervention of spondyloarthritis.
12 anded in synovial tissues from patients with spondyloarthritis.
13 s with chronic back pain and suspected axial spondyloarthritis.
14 ) strongly predisposes to the development of spondyloarthritis.
15 causative in some cases of undifferentiated spondyloarthritis.
16 axis may be involved in the pathogenesis of spondyloarthritis.
17 , diagnosis and management of juvenile-onset spondyloarthritis.
18 th reduced radiographic progression of axial spondyloarthritis.
19 joints increases the diagnostic accuracy of spondyloarthritis.
20 es, including inflammatory bowel disease and spondyloarthritis.
21 d enthesitis-related arthritis (37 [67.3%]), spondyloarthritis (27 [49.1%]), and psoriatic arthritis
23 tis (29% vs 80%, P < .001), undifferentiated spondyloarthritis (58% vs 93%, P < .001) and osteoarthri
24 viously shown efficacy in radiographic axial spondyloarthritis (also known as ankylosing spondylitis)
25 ith rest is the most common symptom of axial spondyloarthritis and affects more than 80% of patients.
26 tients and 109 controls (55 healthy, 54 with spondyloarthritis and connective tissue diseases) were s
27 state of ultrasound imaging with respect to spondyloarthritis and describes some of the limitations
28 With the use of HAART, the prevalence of spondyloarthritis and Diffuse Infiltrative Lymphocytosis
30 allele may contribute to the pathogenesis of spondyloarthritis and its unique phenotype through downs
31 e classification criteria for juvenile-onset spondyloarthritis and magnetic resonance imaging has all
34 ndeed, some 'mixed-pattern' diseases such as spondyloarthritis and some forms of rheumatoid arthritis
35 nflammatory arthritis: rheumatoid arthritis, spondyloarthritis and systemic juvenile idiopathic arthr
36 ical features and overall diagnoses of axial spondyloarthritis, and consequently significantly affect
37 HLA-B27 transgenic) rats, an animal model of spondyloarthritis, and correlated with disease susceptib
39 tes in the blood and joints of patients with spondyloarthritis, and increased numbers of IL-17A(+)GM-
40 okine data in inflammatory bowel disease and spondyloarthritis, and microbiome:immune cell data from
41 ed with human leukocyte antigen B27-negative spondyloarthritis approximately 11 years prior, based on
42 ed with human leukocyte antigen B27-negative spondyloarthritis approximately 11 years prior, based on
43 l fluid-derived monocytes from patients with spondyloarthritis are enriched for IL7R(+) cells with a
44 f bony erosions in patients suspected having spondyloarthritis as compared to the routinely used T1 T
45 A), psoriatic arthritis (PsA) and peripheral spondyloarthritis, as well as of HLA-B27 and other MHC a
55 ity of the broader category now called axial spondyloarthritis (AxSpA) is apparently the opposite.
56 ber of ankylosing spondylitis (AS) and axial spondyloarthritis (axSpA) Registries already in existenc
57 s (PsO), psoriatic arthritis (PsA), or axial spondyloarthritis (axSpA) who received ixekizumab (IXE)
58 o standardize imaging in patients with axial spondyloarthritis (axSpA), few studies have been publish
61 HLA-B27 positive subjects have less active spondyloarthritis compared to HLA-B27 negative subjects
64 or rheumatoid arthritis, osteoarthritis, and spondyloarthritis, digital tomosynthesis detected bone a
65 ous rheumatic syndromes including arthritis, spondyloarthritis, DILS, vasculitides, connective tissue
67 of the interleukin-23/interleukin-17 axis in spondyloarthritis has important therapeutic implications
69 tem associated with rheumatoid arthritis and spondyloarthritis have led to the gut-joint hypothesis,
71 eitis DESIGN: Machine learning of cases with spondyloarthritis/HLA-B27-associated anterior uveitis an
72 was to determine classification criteria for spondyloarthritis/HLA-B27-associated anterior uveitis DE
76 f anterior uveitides, including 184 cases of spondyloarthritis/HLA-B27-associated anterior uveitis, w
77 5, a proton-sensing receptor associated with spondyloarthritis in genome-wide association studies and
79 Older children with psJIA have features of spondyloarthritis, including relative male preponderance
80 ases including systemic lupus erythematosus, spondyloarthritis, inflammatory bowel disease and alopec
81 analysis of MRI scans from the Assessment of SpondyloArthritis International Society (ASAS) classific
82 diagnosis of SpA according to Assessment of SpondyloArthritis International Society (ASAS) criteria
83 commendations developed by the Assessment of SpondyloArthritis International Society (ASAS) that aim
84 th at least 20% improvement in Assessment of Spondyloarthritis International Society (ASAS20) respons
85 proportion of patients with an Assessment of SpondyloArthritis international Society 40 (ASAS40) resp
86 mposite outcome measure of the Assessment of SpondyloArthritis international Society 40 response at w
87 ificantly more patients had an Assessment of SpondyloArthritis international Society 40 response in t
88 The publication of the new Assessment of SpondyloArthritis International Society classification c
90 th back pain who fulfilled the Assessment of SpondyloArthritis International Society criteria for SpA
91 mmatory changes fulfilling the Assessment of SpondyloArthritis international Society definition, and
95 rthritis, as well as psoriatic arthritis and spondyloarthritis, is bringing new insights into the div
98 lled trials (RCTs) in non-radiographic axial spondyloarthritis (nr-axSpA) might be failing to identif
99 graphic sacroiliitis (non-radiographic axial spondyloarthritis), objective signs of inflammation (via
100 ral alternating anterior uveitis with either spondyloarthritis or a positive test result for HLA-B27;
101 h a history of the classic course and either spondyloarthritis or HLA-B27; or 3) anterior uveitis wit
109 matoid arthritis, psoriatic arthritis, axial spondyloarthritis, psoriasis, and inflammatory bowel dis
110 nflammatory arthritis (rheumatoid arthritis, spondyloarthritis, psoriatic arthritis), or psoriasis ta
111 luding 458 adults with rheumatoid arthritis, spondyloarthritis, psoriatic arthritis, ulcerative colit
112 ial of 411 adults with rheumatoid arthritis, spondyloarthritis, psoriatic arthritis, ulcerative colit
113 of individual inflammatory lesions in axial spondyloarthritis (SpA) has not been well established.
116 ss disease activity among 3435 patients with spondyloarthritis (SpA) who participated in a survey des
118 e involvement are rheumatoid arthritis (RA), spondyloarthritis (SpA), and juvenile idiopathic arthrit
119 Gut inflammation is strongly associated with spondyloarthritis (SpA), as exemplified by the high prev
120 diseases like rheumatoid arthritis (RA) and spondyloarthritis (SpA), but the causal mechanisms linki
122 HLA-B*27 confers a strong risk of developing spondyloarthritis (SpA), which includes axial SpA with o
130 The SELECT-AXIS 2 non-radiographic axial spondyloarthritis study was a multicentre, randomised, d
131 -B27 test facilitates the diagnosis of axial spondyloarthritis such that patients from a community su
132 al examination in detecting many features of spondyloarthritis, such as synovitis and enthesitis.
134 ities, medication usage, and side-effects in spondyloarthritis underscores the need for combining dat
135 patients with active non-radiographic axial spondyloarthritis were enrolled into the study, and 313
136 ion for patients with non-radiographic axial spondyloarthritis who had an inadequate response or were
137 ble adults had active non-radiographic axial spondyloarthritis, with objective signs of inflammation
138 e adults (aged >=18 years) with active axial spondyloarthritis without definite radiographic sacroili