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1 aphic axial spondyloarthritis (also known as ankylosing spondylitis).
2 ic target for autoimmune diseases, including ankylosing spondylitis.
3 f exercise and nonpharmacologic therapies in ankylosing spondylitis.
4 on may be of benefit to select patients with ankylosing spondylitis.
5 psoriatic arthritis, reactive arthritis, or ankylosing spondylitis.
6 espect to understanding the genetic basis of ankylosing spondylitis.
7 pus erythematosus, rheumatoid arthritis, and ankylosing spondylitis.
8 ists are effective for signs and symptoms of ankylosing spondylitis.
9 s and spinal deformities similar to those in ankylosing spondylitis.
10 en shown to be effective in the treatment of ankylosing spondylitis.
11 dissection of the genetic susceptibility to ankylosing spondylitis.
12 otential role in delaying the progression of ankylosing spondylitis.
13 itis and to attenuate spinal inflammation in ankylosing spondylitis.
14 antagonists can prevent structural damage in ankylosing spondylitis.
15 b were also effective in phase III trials in ankylosing spondylitis.
16 thritis can be asymptomatic, as in classical ankylosing spondylitis.
17 , inflammatory bowel diseases, psoriasis, or ankylosing spondylitis.
18 or (p75):Fc fusion protein, in patients with ankylosing spondylitis.
19 , and sustained improvement in patients with ankylosing spondylitis.
20 in Sardinia, seem not to be associated with ankylosing spondylitis.
21 children or siblings of female patients with ankylosing spondylitis.
22 pathway is a potential therapeutic target in ankylosing spondylitis.
23 report human TRBV9(+) T cell elimination in ankylosing spondylitis.
24 a selective JAK1 inhibitor, in patients with ankylosing spondylitis.
25 ons like psoriasis, psoriatic arthritis, and ankylosing spondylitis.
26 been shown to be effective in patients with ankylosing spondylitis.
27 icrobiome are associated with development of ankylosing spondylitis.
28 sistent with the overall lack of efficacy in ankylosing spondylitis.
29 ondyloarthropathies, psoriatic arthritis and ankylosing spondylitis.
30 rials of secukinumab in patients with active ankylosing spondylitis.
31 ording to the modified New York criteria for ankylosing spondylitis.
32 s Crohn's disease, rheumatoid arthritis, and ankylosing spondylitis.
33 e epistatic association of both molecules in ankylosing spondylitis.
34 orm of axial spondyloarthropathies, which is ankylosing spondylitis.
35 -7.0) for psoriasis, psoriatic arthritis, or ankylosing spondylitis.
36 -B27 subtypes differentially associated with ankylosing spondylitis.
37 inflammatory diseases, notably psoriasis and ankylosing spondylitis.
38 th inflammatory bowel disease, psoriasis and ankylosing spondylitis.
39 ythematosus (1346+/-1011 pg per milliliter), ankylosing spondylitis (1368+/-1162 pg per milliliter),
40 ges of patients achieving the Assessments in Ankylosing Spondylitis 20% response (ASAS20) at weeks 12
41 improved significantly after MR imaging for ankylosing spondylitis (29% vs 80%, P < .001), undiffere
43 ren of women had an even higher incidence of ankylosing spondylitis (7.2 [1.5-34], p=0.013) than did
44 an [SD] age, 48.8 [12.1] years), and 977 had ankylosing spondylitis (7.3%; 658 men [67.3%]; mean [SD]
45 relationship between the gut microbiome and ankylosing spondylitis, a quantitative metagenomics stud
46 Evaluating Long-Term Efficacy and Safety in Ankylosing Spondylitis, a randomized controlled study, w
49 residues 528 and 575/725 is associated with ankylosing spondylitis among HLA-B27-positive individual
50 riteria for PsA, a new composite measure for ankylosing spondylitis and axial SpA, the ASDAS, new mea
52 dies of various physical therapy programs in ankylosing spondylitis and identify their benefits and p
53 has supported novel roles for these drugs in ankylosing spondylitis and in cancer prevention, accumul
54 bserved in phase III trials of patients with ankylosing spondylitis and in trials conducted a decade
56 ecent studies indicate that the morbidity of ankylosing spondylitis and PsA are considerably higher t
58 uding rheumatoid arthritis, Crohn's disease, ankylosing spondylitis and psoriasis, confirms the impor
61 of the tumor necrosis factor antagonists in ankylosing spondylitis and psoriatic arthritis has gener
62 necrosis factor inhibitors for patients with ankylosing spondylitis and psoriatic arthritis has had a
63 Sulfasalazine is moderately effective for ankylosing spondylitis and psoriatic arthritis, although
70 ole for HLA-B27 in genetic susceptibility to ankylosing spondylitis and related spondyloarthropathies
71 cal comparison with originator infliximab in ankylosing spondylitis and rheumatoid arthritis; however
72 ons within major histocompatibility complex (ankylosing spondylitis and sacroiliitis, P = 1.4E-15; OR
73 absence of EIMs (eg, ankylosing spondylitis [ankylosing spondylitis and sacroiliitis], primary sclero
74 ing psoriatic arthritis, reactive arthritis, ankylosing spondylitis), and osteoarthritis have charact
77 ch as rheumatoid arthritis, IgA nephropathy, ankylosing spondylitis, and inflammatory bowel disease (
78 anding inflammation in rheumatoid arthritis, ankylosing spondylitis, and juvenile chronic arthritis.
79 tion may have structure-modifying effects in ankylosing spondylitis, and may thereby alter the diseas
80 immune diseases such as behcet's disease and ankylosing spondylitis, and ocular involvement of infect
83 nvestigated one in detail, a risk allele for ankylosing spondylitis, and provide direct evidence of a
84 indications (psoriatic arthritis, psoriasis, ankylosing spondylitis, and rheumatoid arthritis), we te
85 erextensibility, early onset osteoarthritis, ankylosing spondylitis, and seronegative erosive rheumat
86 py not only in RA but also in Crohn disease, ankylosing spondylitis, and several other chronic inflam
87 lgia rheumatica (PMR), giant cell arteritis, ankylosing spondylitis, and Sjogren's syndrome, and to p
88 e of the spondyloarthritides, including PsA, ankylosing spondylitis, and the broader categories of Sp
89 the disease-modifying role of these drugs in ankylosing spondylitis, and their use in the understudie
90 s, two patients with gout, two patients with ankylosing spondylitis, and two patients with psoriatic
91 cases with presence or absence of EIMs (eg, ankylosing spondylitis [ankylosing spondylitis and sacro
93 or rheumatoid arthritis, where patients with ankylosing spondylitis are offered therapy early in the
96 h American sample of two new loci related to ankylosing spondylitis, ARTS1 and IL23R, and confirmatio
97 systemic lupus erythematosus (SLE) (n = 10), ankylosing spondylitis (AS) (n = 10), primary Sjogren's
99 strated similarities and differences between ankylosing spondylitis (AS) and axial psoriatic arthriti
100 s detailing their application in a number of ankylosing spondylitis (AS) and axial spondyloarthritis
101 mography (MDCT) findings of 41 patients with ankylosing spondylitis (AS) and compared them with pulmo
102 rongly associated with predisposition toward ankylosing spondylitis (AS) and other spondyloarthropath
103 e autoimmune inflammatory arthritis disorder ankylosing spondylitis (AS) and with other related spond
105 ) affects approximately 40% of patients with ankylosing spondylitis (AS) but also affects patients wi
106 iasis (PSOR), psoriatic arthritis (PsA), and ankylosing spondylitis (AS) from 526 subjects overall.
108 tients with MRI-evident sacroiliitis develop ankylosing spondylitis (AS) in the long term and whether
116 erstanding of the gene-regulatory network in ankylosing spondylitis (AS) is vital for elucidating the
119 ment of spinal inflammation in patients with ankylosing spondylitis (AS) relies primarily on magnetic
120 udies of the HLA-B27-transgenic rat model of ankylosing spondylitis (AS) suggested that macrophages d
122 seases of the spine and pelvis (for example, ankylosing spondylitis (AS)) and the eye (that is, acute
123 7 subtypes associated with susceptibility to ankylosing spondylitis (AS), and those reported not to b
124 HC) tag SNPs from 1,000 independent cases of ankylosing spondylitis (AS), autoimmune thyroid disease
125 s I molecule B27 is strongly associated with ankylosing spondylitis (AS), but the pathogenic role of
126 rated high heritability of susceptibility to ankylosing spondylitis (AS), it is only recently that th
127 ld standard of rheumatologists' diagnosis of ankylosing spondylitis (AS), psoriatic arthritis (PsA),
128 l and peripheral articular manifestations of ankylosing spondylitis (AS), psoriatic arthritis (PsA),
129 negative spondyloarthropathies (SpA) include ankylosing spondylitis (AS), psoriatic arthritis (PsA),
130 endoplasmic reticulum aminopeptidase 1) with ankylosing spondylitis (AS), which is restricted to HLA-
141 TNFis) have revolutionized the management of ankylosing spondylitis (AS); however, the lack of notabl
142 ciated with the chronic inflammatory disease Ankylosing Spondylitis (AS); however, the mechanisms und
144 with unlike conformations in differentially ankylosing spondylitis-associated subtypes) must not be
147 a prospective study involving patients with ankylosing spondylitis, behcet's disease, presumed sarco
148 e for relieving the pain of axial disease in ankylosing spondylitis but these findings contradict two
149 eased susceptibility and disease activity of ankylosing spondylitis, but the effect of HLA-B27 on the
150 me-wide association study in 2,053 unrelated ankylosing spondylitis cases among people of European de
152 changes in the course of the disease, Stoke Ankylosing spondylitis classification Spinal Score (SASS
153 eously investigated the genetic landscape of ankylosing spondylitis, Crohn's disease, psoriasis, prim
155 0 patients and 45 controls: alopecia areata, ankylosing spondylitis, dermatomyositis, Graves' disease
156 oth M-CSF and MMP-3 correlated with the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) v
158 cal disease activity as measured by the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI),
159 onset, disease activity assessed by the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI),
160 ondylitis Functional Index (BASFI), the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI),
161 Disease activity was assessed using the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI).
162 ter disease activity as measured by the Bath Ankylosing Spondylitis Disease Activity Index (P = 0.002
163 ase activity and functional parameters (Bath Ankylosing Spondylitis Disease Activity Index [BASDAI],
164 s (EAIR, 0.02; 95% CI, 0.00-0.11), and 2 had ankylosing spondylitis (EAIR, 0.08; 95% CI, 0.01-0.28).
165 nthesitis (using the PsA-modified Maastricht Ankylosing Spondylitis Enthesitis Score [MASES] index).
166 ce of rheumatoid arthritis, Crohn's disease, ankylosing spondylitis, familial Mediterranean fever, an
167 rmatomyositis; 16 had scleroderma; eight had ankylosing spondylitis; five had juvenile RA; three had
168 ose with psoriatic arthritis, and those with ankylosing spondylitis from phase III trials of golimuma
170 al assessments included the BASDAI, the Bath Ankylosing Spondylitis Functional Index (BASFI), the Ank
171 ght, VAS scores for entheseal pain, the Bath Ankylosing Spondylitis Functional Index (BASFI), the Bat
173 nal limitations were assessed using the Bath Ankylosing Spondylitis Functional Index (BASFI; score ra
174 ylitis Disease Activity Index [BASDAI], Bath Ankylosing Spondylitis Functional Index [BASFI], and Bat
176 etween inflammation and structural damage in ankylosing spondylitis has been an important focus of re
178 ive arthritis, but an infectious trigger for ankylosing spondylitis has not yet been established.
179 d for patients with rheumatoid arthritis and ankylosing spondylitis have been reported, and generic q
183 that TNFi slows radiographic progression in ankylosing spondylitis in data from clinical trials may
186 principle has relevance to diseases such as ankylosing spondylitis, in which HLA-B27 and ERAP jointl
187 une hemolytic anemia, pernicious anemia, and ankylosing spondylitis), infectious (pneumonia, hepatiti
188 f Life (ASQoL) instrument, the ASsessment in Ankylosing Spondylitis International Working Group crite
193 IL-1A association further substantiate that ankylosing spondylitis is determined to a large extent b
194 modified New York criteria, the diagnosis of ankylosing spondylitis is made based on the presence of
198 rthritis, psoriasis/psoriatic arthritis, and ankylosing spondylitis) linked to newborns with periconc
199 autoimmune disease and evidence showed that ankylosing spondylitis may be a microbiome-driven diseas
201 with many immune-mediated diseases including ankylosing spondylitis, multiple sclerosis, and inflamma
202 = 8), juvenile rheumatoid arthritis (n = 3), ankylosing spondylitis (n = 1), and psoriatic spondylart
203 pproval of Janus kinase (JAK) inhibitors for ankylosing spondylitis, new data on the effect of biolog
204 , rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, non-infectious uveitis, and mult
205 ebo-controlled RCTs of rheumatoid arthritis, ankylosing spondylitis, optic neuritis, systemic lupus e
206 = 1.33; 95% CI, 1.03-1.72) and negative for ankylosing spondylitis (OR = 0.72; 95% CI, 0.54-0.98) an
207 d arthritis, psoriasis, psoriatic arthritis, ankylosing spondylitis, or inflammatory bowel disease us
208 indications (psoriasis, psoriatic arthritis, ankylosing spondylitis, or juvenile arthritis), as an ac
209 adults diagnosed with rheumatoid arthritis, ankylosing spondylitis, or psoriatic arthritis and 219 h
210 wel disease, psoriasis, psoriatic arthritis, ankylosing spondylitis, or rheumatoid arthritis exhibite
211 d IL12B regions convincingly associated with ankylosing spondylitis (P < 5 x 10(-8) in the combined d
212 tients with presumed sarcoidosis compared to ankylosing spondylitis (p = 0.0001), behcet's disease (p
213 ts with presumed sarcoidosis with respect to ankylosing spondylitis (p = 0.0001), behcet's disease, (
215 shown to be differentially abundant between ankylosing spondylitis patients and healthy controls.
221 e advances in the pharmacological therapy of ankylosing spondylitis, physical therapy remains an esse
222 RS had a higher significant association with ankylosing spondylitis, polymyositis, psoriasis, rheumat
223 carrying of the spinal cord in the course of ankylosing spondylitis, present in MRI include: bone mar
224 dently linked to inflammatory bowel disease, ankylosing spondylitis, primary sclerosing cholangitis a
225 n the pathogenesis or development process of ankylosing spondylitis, providing new leads for the deve
226 IBD), and psoriasis, psoriatic arthritis, or ankylosing spondylitis (psoriasis and spondyloarthropath
227 Group criteria for SpA, without evidence of ankylosing spondylitis, psoriasis, inflammatory bowel di
228 recently associated with the pathogenesis of ankylosing spondylitis, psoriatic arthritis and acute an
229 ct in the treatment of rheumatoid arthritis, ankylosing spondylitis, psoriatic arthritis, and juvenil
230 ts and for diseases other than RA, including ankylosing spondylitis, psoriatic arthritis, and polymyo
231 mmatory bowel disease, rheumatoid arthritis, ankylosing spondylitis, psoriatic arthritis, and psorias
232 mmatory bowel disease, rheumatoid arthritis, ankylosing spondylitis, psoriatic arthritis, and psorias
233 uded in the category of spondyloarthropathy (ankylosing spondylitis, psoriatic arthritis, reactive ar
234 ng Spondylitis Functional Index (BASFI), the Ankylosing Spondylitis Quality of Life (ASQoL) instrumen
235 the Short Form 36 (SF-36) Health Survey and Ankylosing Spondylitis Quality of Life (ASQoL) Questionn
236 tis Disease Activity Index (BASDAI), and the Ankylosing Spondylitis Quality of Life (ASQoL) questionn
237 lvis, and hips were scored by using the Bath Ankylosing Spondylitis Radiology Index (BASRI) by an exp
238 pinal radiographs were scored using the Bath Ankylosing Spondylitis Radiology Index for the spine (BA
239 ry rheumatic diseases that primarily include ankylosing spondylitis, reactive arthritis, and the arth
241 rheumatological conditions (i.e. psoriasis, ankylosing spondylitis, rheumatoid arthritis, fibromyalg
242 keletal disorders, including osteoarthritis, ankylosing spondylitis, rheumatoid arthritis, heterotopi
243 dy reports four genetic loci associated with ankylosing spondylitis risk and identifies a major role
244 before HLA class I presentation, only affect ankylosing spondylitis risk in HLA-B27-positive individu
246 ccess in psoriasis, psoriatic arthritis, and ankylosing spondylitis, sparking efforts to develop oral
248 biologic DMARDs on structural progression in ankylosing spondylitis, strategy trials on tapering or s
249 of the interleukin-1 (IL-1) region genes in ankylosing spondylitis suggested the susceptibility to b
250 A recent meta-analysis of published scans of ankylosing spondylitis susceptibility has confirmed site
251 on-major histocompatibility complex genes in ankylosing spondylitis susceptibility, and suggests area
253 r psoriatic arthritis, rheumatoid arthritis, ankylosing spondylitis, systemic lupus erythematosus, an
254 , psoriatic arthritis, rheumatoid arthritis, ankylosing spondylitis, systemic lupus erythematosus, Sj
255 c lupus erythematosus, rheumatoid arthritis, ankylosing spondylitis, systemic sclerosis, Sjogren synd
256 nt GWAS on multiple sclerosis, psoriasis and ankylosing spondylitis that inclusion of known covariate
257 able and effective structure modification in ankylosing spondylitis, the data strongly suggest a bene
259 ide strong evidence that HLA-B27 operates in ankylosing spondylitis through a mechanism involving abe
260 Exercise therapy should remain a mainstay of ankylosing spondylitis treatment complementing medical t
261 durations may result in a paradigm shift for ankylosing spondylitis treatment similar to that undergo
262 gone substantial change from when the entity ankylosing spondylitis was defined by the modified New Y
265 50% and 75% of patients were diagnosed with ankylosing spondylitis were ascertained from a database
266 Forty patients with active, inflammatory ankylosing spondylitis were randomly assigned to receive
267 e SpA (2 with psoriatic arthritis and 1 with ankylosing spondylitis) were isolated by positive select
268 cantly reduces spinal inflammation in active ankylosing spondylitis when compared to placebo; there w
270 atibility complex genes in predisposition to ankylosing spondylitis, which will be summarized here.
271 s and well tolerated in patients with active ankylosing spondylitis who had an inadequate response or
273 and women differ in their susceptibility to ankylosing spondylitis, with about 2.5 men affected for
274 de over 90% of the overall susceptibility to ankylosing spondylitis, with about half of the genetic c
275 esitis-related arthritis progress to develop ankylosing spondylitis within 10 years after presentatio