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1 estigation of bimekizumab as a treatment for psoriatic arthritis.
2 se of selective inhibition of IL-23 to treat psoriatic arthritis.
3 ne that is implicated in the pathogenesis of psoriatic arthritis.
4 veitis, mild psoriasis, severe psoriasis, or psoriatic arthritis.
5 ses IL17A and IL17F, in patients with active psoriatic arthritis.
6 in-17A monoclonal antibody, in patients with psoriatic arthritis.
7 -17A receptor improved signs and symptoms of psoriatic arthritis.
8 sis of uveitis for the risk for psoriasis or psoriatic arthritis.
9 improved response rates among patients with psoriatic arthritis.
10 ebo-controlled study involving patients with psoriatic arthritis.
11 er investigation of ustekinumab's effects on psoriatic arthritis.
12 icacy of ustekinumab in patients with active psoriatic arthritis.
13 patients aged at least 18 years with active psoriatic arthritis.
14 ncestry with multiple cases of psoriasis and psoriatic arthritis.
15 kinumab efficacy and safety for treatment of psoriatic arthritis.
16 l symptoms and pathological joint changes of psoriatic arthritis.
17 dependent target in therapy of psoriasis and psoriatic arthritis.
18 being developed to characterize and stratify psoriatic arthritis.
19 sease, and a seronegative arthritis known as psoriatic arthritis.
20 ce has accrued in ankylosing spondylitis and psoriatic arthritis.
21 uality of life in ankylosing spondylitis and psoriatic arthritis.
22 tor inhibitors in ankylosing spondylitis and psoriatic arthritis.
23 the treatment of ankylosing spondylitis and psoriatic arthritis.
24 n protein, is FDA approved for psoriasis and psoriatic arthritis.
25 statistical significance in the treatment of psoriatic arthritis.
26 s is most apparent in juvenile arthritis and psoriatic arthritis.
27 atment of psoriasis and have been studied in psoriatic arthritis.
28 of non-steroidal anti-inflammatory drugs for psoriatic arthritis.
29 sociated with both early-onset psoriasis and psoriatic arthritis.
30 en shown equally in rheumatoid arthritis and psoriatic arthritis.
31 thritis appears to be strongly suggestive of psoriatic arthritis.
32 nsitive and quantitatively discriminative in psoriatic arthritis.
33 al models and human rheumatoid arthritis and psoriatic arthritis.
34 c modifiers such as CARD15 may predispose to psoriatic arthritis.
35 s also have joint involvement, indicative of psoriatic arthritis.
36 ies of patients with rheumatoid arthritis or psoriatic arthritis.
37 nd 20-30% of individuals with psoriasis have psoriatic arthritis.
38 recently, was licensed for the treatment of psoriatic arthritis.
39 ors, thereby contributing to pathogenesis of psoriatic arthritis.
40 f RA and, more recently, for juvenile RA and psoriatic arthritis.
41 , and idiopathic inflammatory arthritis), or psoriatic arthritis.
42 n used to distinguish between rheumatoid and psoriatic arthritis.
43 r the experimental approach to mechanisms in psoriatic arthritis.
44 ic susceptibility may underlie psoriasis and psoriatic arthritis.
45 s most significant in those families without psoriatic arthritis.
46 on making in the management of patients with psoriatic arthritis.
47 s guselkumab in biologic-naive patients with psoriatic arthritis.
48 ve treatment option for patients with active psoriatic arthritis.
49 cutaneous psoriasis, psoriasis vulgaris and psoriatic arthritis.
50 IL-17 are also approved for the treatment of psoriatic arthritis.
51 is a potential novel therapeutic approach in psoriatic arthritis.
52 a but instead resulted in the development of psoriatic arthritis.
53 Particular risk factors included sex and psoriatic arthritis.
54 is under investigation for the treatment of psoriatic arthritis.
55 nsight into the cellular immune landscape of psoriatic arthritis.
56 and patients with ankylosing spondylitis and psoriatic arthritis.
57 ant in the development of conditions such as psoriatic arthritis.
58 hese approaches have not yet been studied in psoriatic arthritis.
59 s erythematosus, 20 with vasculitis, 18 with psoriatic arthritis, 16 with scleroderma, and 261 with v
63 riasis (and 1 who also developed features of psoriatic arthritis) after receiving rituximab for a var
64 ritis and the group with mild psoriasis with psoriatic arthritis also had an increased risk of incide
65 ely effective for ankylosing spondylitis and psoriatic arthritis, although the large placebo response
66 e lack of agreed classification criteria for psoriatic arthritis; although in both adult and juvenile
67 with RA and 3 with seronegative SpA (2 with psoriatic arthritis and 1 with ankylosing spondylitis) w
70 psoriasis (including 10107 with concomitant psoriatic arthritis and 137847 without psoriatic arthrit
73 significantly reduced signs and symptoms of psoriatic arthritis and diminished skin lesions compared
75 ritis, undifferentiated spondyloarthropathy, psoriatic arthritis and juvenile spondyloarthropathy.
76 eye symptoms in patients with psoriasis and psoriatic arthritis and on skin and joint symptoms in pa
77 the first-line drug for the treatment of RA, psoriatic arthritis and other forms of inflammatory arth
78 ed IL-23/IL-17 responses have been linked to psoriatic arthritis and other forms of spondyloarthritid
79 ets interleukin-17A, in patients with active psoriatic arthritis and previous inadequate response to
86 ic studies did not find associations between psoriatic arthritis and several class I major histocompa
87 l tissue in rheumatoid arthritis, as well as psoriatic arthritis and spondyloarthritis, is bringing n
88 ed 18 years or older with active adult-onset psoriatic arthritis and symptoms for at least 6 months w
90 n 2.9 ng/ml, IQR 0.9 ng/ml) of patients with psoriatic arthritis and the plasma of healthy control su
91 progression of radiographic joint damage in psoriatic arthritis and to attenuate spinal inflammation
92 inflammatory features, such as enthesitis in psoriatic arthritis and uveitis in ankylosing spondyliti
93 e signs and symptoms of patients with active psoriatic arthritis and who had previously inadequate re
94 itant psoriatic arthritis and 137847 without psoriatic arthritis) and 147954 nonpsoriatic controls.
95 I patients (12 rheumatoid arthritis [RA], 12 psoriatic arthritis, and 12 systemic sclerosis) were rec
96 t of moderate-to-severe plaque psoriasis and psoriatic arthritis, and further agents are currently in
97 s immunological disorders such as psoriasis, psoriatic arthritis, and inflammatory bowel diseases.
98 heumatoid arthritis, ankylosing spondylitis, psoriatic arthritis, and juvenile idiopathic arthritis a
99 r than RA, including ankylosing spondylitis, psoriatic arthritis, and polymyositis, in 36 patients.
100 was recently approved to treat psoriasis and psoriatic arthritis, and related agents are in clinical
101 consideration of the extent of skin disease, psoriatic arthritis, and severity of nail disease with c
102 tients with rheumatoid arthritis, those with psoriatic arthritis, and those with ankylosing spondylit
104 asis, Crohn's disease, rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, non-infecti
105 older with rheumatoid arthritis, psoriasis, psoriatic arthritis, ankylosing spondylitis, or inflamma
109 ased focus on the diagnosis and treatment of psoriatic arthritis as newer and more effective drugs th
110 Recognition of the immunopathogenesis of psoriatic arthritis, as with rheumatoid arthritis and ps
112 enrolled biologic-naive patients with active psoriatic arthritis (at least five swollen joints, at le
113 orth America and enrolled adults with active psoriatic arthritis (at least three swollen and three te
115 ntly increased in frequency in patients with psoriatic arthritis, but not in those with psoriasis.
116 KIR2DS2 genes are susceptible to developing psoriatic arthritis, but only when HLA ligands for their
117 dered understanding of disease mechanisms in psoriatic arthritis, but recent studies have provided in
119 ammation and specifically the development of psoriatic arthritis by impeding the Adam17-mediated rele
121 ted with a number of comorbidities including psoriatic arthritis, cardiometabolic diseases, and depre
123 Ustekinumab significantly improved active psoriatic arthritis compared with placebo, and might off
125 for Research and Assessment of Psoriasis and Psoriatic Arthritis Composite Exercise cohort was used f
127 multiple sclerosis, hepatitis C, psoriasis, psoriatic arthritis, Crohn's disease, or ulcerative coli
128 kumab in biologic-naive patients with active psoriatic arthritis (DISCOVER-2): a double-blind, random
130 at Fhl2-deficient mice develop a more severe psoriatic arthritis disease under induction of the induc
134 years or older, had a confirmed diagnosis of psoriatic arthritis for at least 6 months, and had a pre
135 epresent a physiologically relevant model of psoriatic arthritis for understanding disease progressio
136 Diagnosis of mild or severe psoriasis or psoriatic arthritis for uveitis risk and diagnosis of uv
138 merica, and Asia-Pacific, adults with active psoriatic arthritis (>/=5 tender and >/=5 swollen joints
139 nd that the group with severe psoriasis with psoriatic arthritis had the greatest risk of incident uv
140 or antagonists in ankylosing spondylitis and psoriatic arthritis has generated considerable enthusias
141 for patients with ankylosing spondylitis and psoriatic arthritis has had a tremendous impact on daily
146 , psoriasis (HR 0.58 [95% CI 0.10-3.31]), or psoriatic arthritis (HR 0.74 [95% CI 0.20-2.76]) during
148 umatoid arthritis in 3.9%, and psoriasis and psoriatic arthritis in (6.3%) [corrected], atopy (allerg
152 the incidence and prognosis of psoriasis and psoriatic arthritis in patients undergoing bariatric sur
155 randomly sampled patients with psoriasis and psoriatic arthritis in the US population from a database
164 er, increased body mass index, nail disease, psoriatic arthritis, larger plaques, more body sites, an
167 adult patients (aged >/=18 years) with early psoriatic arthritis (<24 months symptom duration), who h
168 oval by the Food and Drug Administration for psoriatic arthritis management are safe and effective in
170 t that the uveitis that accompanies juvenile psoriatic arthritis might be a distinct disease that is
171 , juvenile chronic arthritis (JCA) (n = 13), psoriatic arthritis (n = 9), rheumatoid arthritis (RA) (
172 e patients who were HLA-C*06:02 positive and psoriatic arthritis negative demonstrated significantly
173 ion, dyslipidemia, type 2 diabetes mellitus, psoriatic arthritis, nonalcoholic fatty liver disease, d
174 nkylosing spondylitis, and two patients with psoriatic arthritis, only one of whom was infected with
176 s that resulted in disabling flares of known psoriatic arthritis or unmasked previously occult joint
177 ase (OR 0.81 [95% CI 0.70-0.94]; p < 0.005), psoriatic arthritis (OR 1.36 [95% CI 1.00-1.84]; p < 0.0
179 ammatory bowel disease (IBD), and psoriasis, psoriatic arthritis, or ankylosing spondylitis (psoriasi
181 comes were incident (new-onset) psoriasis or psoriatic arthritis, or progression to severe psoriasis.
183 sting efficacy for both plaque psoriasis and psoriatic arthritis, our case series raises concern that
187 Confirmation was sought in 199 psoriasis and psoriatic arthritis patients from Toronto who were follo
189 kin disease, including genital psoriasis and psoriatic arthritis patients, also had increased IL-19,
190 fluid from RA and OA patients compared with psoriatic arthritis patients, whereas RNase activity of
192 ritis, such as rheumatoid arthritis (RA) and psoriatic arthritis, periodontitis and peri-prosthetic l
194 ses, including systemic lupus erythematosus, psoriatic arthritis, polymyalgia rheumatica (PMR), giant
195 us on chromosome 16 are also associated with psoriatic arthritis, providing support for a model invol
196 n this double-blind study, 127 patients with psoriatic arthritis (PsA) and active psoriasis were rand
197 joint arthropathy is characteristic of both psoriatic arthritis (PsA) and osteoarthritis (OA), but t
198 examine its pathophysiologic significance in psoriatic arthritis (PsA) and rheumatoid arthritis (RA).
199 erging treatments and treatment paradigms of psoriatic arthritis (PsA) and spondyloarthritis (SpA).
200 n in synovial membrane (SM) of patients with psoriatic arthritis (PsA) compared with that in skin of
210 in reducing the signs and symptoms of active psoriatic arthritis (PsA) through week 24 of the GO-REVE
211 f patients with RA, osteoarthritis (OA), and psoriatic arthritis (PsA) to determine OPN-R, OPN-L, and
212 Up to 30% of the patients with PS develop psoriatic arthritis (PsA), a condition characterized by
213 ing receptors were susceptible to developing psoriatic arthritis (PsA), an effect that was strongest
214 to 30% of people with PsV eventually develop psoriatic arthritis (PsA), an inflammatory musculoskelet
215 arly rheumatoid arthritis (RA), 12 had early psoriatic arthritis (PsA), and 10 had osteoarthritis (OA
216 4 inhibitor apremilast in psoriasis (PSOR), psoriatic arthritis (PsA), and ankylosing spondylitis (A
219 enile idiopathic arthritis (JIA), psoriasis, psoriatic arthritis (PsA), and multiple sclerosis (MS),
220 thritis (OA), juvenile idiopathic arthritis, psoriatic arthritis (PsA), and RA were quantified by enz
221 nifestations of ankylosing spondylitis (AS), psoriatic arthritis (PsA), and reactive arthritis (ReA;
222 r incident liver disease in psoriasis (PsO), psoriatic arthritis (PsA), and rheumatoid arthritis (RA)
223 y effective in rheumatoid arthritis (RA) and psoriatic arthritis (PsA), but a significant number of p
224 patients with rheumatoid arthritis (RA) and psoriatic arthritis (PsA), but not osteoarthritis (OA),
225 s' diagnosis of ankylosing spondylitis (AS), psoriatic arthritis (PsA), or reactive arthritis (ReA):
226 rms of arthritis (rheumatoid arthritis (RA), psoriatic arthritis (PsA), osteoarthritis (OA)) or chron
227 s (SpA) include ankylosing spondylitis (AS), psoriatic arthritis (PsA), reactive arthritis, the arthr
228 ternational diagnostic standard for juvenile psoriatic arthritis (PsA), replacing the less-restrictiv
238 risk of two major clinical subtypes of PsV, psoriatic arthritis (PsA; n = 3,038) and cutaneous psori
240 ariables included age, sex, body mass index, psoriatic arthritis, psychiatric disorders, and comorbid
241 a seronegative spondyloarthropathy, such as psoriatic arthritis, reactive arthritis, or ankylosing s
242 spondyloarthropathy (ankylosing spondylitis, psoriatic arthritis, reactive arthritis, undifferentiate
243 18-86 years) with psoriasis, with or without psoriatic arthritis, receiving conventional IT and/or bi
244 and cholestasis in a 48-year-old female with psoriatic arthritis, receiving methotrexate and inflixim
245 ndertreatment of patients with psoriasis and psoriatic arthritis remain a significant problem in the
251 luded the proportion of patients who met the Psoriatic Arthritis Response Criteria (PsARC) and who me
252 All three loci were also associated with psoriatic arthritis (rs4795067, combined P = 1 x 10; rs1
253 p19 subunit binding, significantly improved psoriatic arthritis signs and symptoms with an acceptabl
254 otably radiographic outcome in patients with psoriatic arthritis, so that stratified medicine approac
255 nd 150 mg improved the signs and symptoms of psoriatic arthritis, suggesting that secukinumab is a po
256 he major histocompatibility complex (MHC) to psoriatic arthritis susceptibility resembles that in pso
257 that B*38:01 and B*08 may be associated with psoriatic arthritis susceptibility, and that allotypes e
258 developed and cross-sectional evaluations of psoriatic arthritis synovia in the context of other arth
261 othelial growth factor and angiopoietin 2 in psoriatic arthritis synovial vasculature may provide ins
262 metalloproteinases are strongly expressed in psoriatic arthritis synovium, and serum matrix metallopr
263 l inspection of RA, osteoarthritis (OA), and psoriatic arthritis synovium, exRNA was detectable only
264 port for distinct pathogenetic mechanisms in psoriatic arthritis that arise from a complex interplay
266 Extrapolating from studies on adults with psoriatic arthritis, the mechanism of older-onset PsJIA
267 r positivity does not exclude a diagnosis of psoriatic arthritis--the single most important clinical
269 We randomly assigned patients with active psoriatic arthritis to receive brodalumab (140 or 280 mg
270 Ustekinumab is approved for psoriasis and psoriatic arthritis treatment and has been successfully
271 tanercept slowed radiographic progression in psoriatic arthritis trials, but it is not known whether
273 assess the effect of tight control on early psoriatic arthritis using a treat-to-target approach.
274 incident uveitis with mild psoriasis without psoriatic arthritis was not identified (adjusted hazard
276 human stratum corneum found in patients with psoriatic arthritis was shown to be different from AKA.
278 ts with psoriasis and 45.5% of patients with psoriatic arthritis were dissatisfied with their treatme
280 A, adults (aged >/=18 years old) with active psoriatic arthritis were randomly allocated in a 1:1:1:1
282 uble-blind, phase 3 study, 606 patients with psoriatic arthritis were randomly assigned in a 1:1:1 ra
283 ReA, 1 with rheumatoid arthritis, and 1 with psoriatic arthritis) were positive for C. trachomatis.
284 risk and improved prognosis of psoriasis and psoriatic arthritis, whereas gastric banding was not.
285 with psoriasis and patients with concurrent psoriatic arthritis, whereas men with psoriasis had part
286 e data published in 2004 on the treatment of psoriatic arthritis, which arthritis affects 6 to 39% of
287 more effective than placebo in patients with psoriatic arthritis, which validates interleukin-17A as
288 oped digit arthritis with features common to psoriatic arthritis, while mice expressing point mutatio
289 In this trial involving patients with active psoriatic arthritis who had had an inadequate response t
290 that of placebo at month 3 in patients with psoriatic arthritis who had previously had an inadequate
291 valuated tofacitinib in patients with active psoriatic arthritis who had previously had an inadequate
292 valuated tofacitinib in patients with active psoriatic arthritis who previously had an inadequate res
293 benefit-risk profile in patients with active psoriatic arthritis who were naive to treatment with bio
294 t modalities are available for psoriasis and psoriatic arthritis, widespread treatment dissatisfactio
297 and that proposed treatment of psoriasis and psoriatic arthritis with rituximab may result in unpredi
298 ithin this disease group and the relation of psoriatic arthritis with the other spondyloarthropathies
299 therapy for 52 weeks in patients with active psoriatic arthritis, with a musculoskeletal primary endp
300 for spondyloarthropathy exist, the place of psoriatic arthritis within this larger group requires fu