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1 l bone marrow edema, synovitis, bursitis, or enthesitis.
2 ce, increased risk of axial involvement, and enthesitis.
3 tween bone erosion and new bone formation in enthesitis.
4 of spondyloarthritis, such as synovitis and enthesitis.
5 ans rarely confirm the clinical diagnosis of enthesitis.
6 -seven patients with SpA and Achilles tendon enthesitis (20 with early SpA and 17 with chronic SpA) a
7 al SpA with or without peripheral arthritis, enthesitis, acute anterior uveitis and gastrointestinal
9 his is associated with marked improvement of enthesitis and associated osteitis pathology as determin
13 e specific and characteristic development of enthesitis and entheseal new bone formation in the initi
14 of pathological lesions was not specific to enthesitis and might more likely correspond to degenerat
15 for inflammatory changes (bone marrow edema, enthesitis) and structural changes (erosions, sclerosis)
16 g the mechanisms that underlie angiogenesis, enthesitis, and bone resorption in psoriatic arthritis a
18 oint count, evaluation for dactylitis and/or enthesitis, and skin examination) and HLA-B27 typing wer
20 In contrast, older patents tend to manifest enthesitis, axial joint disease, and persistent oligoart
21 , spinal pain, functioning, quality of life, enthesitis, chest expansion, erythrocyte sedimentation r
22 litis, seronegative ankylosing arthritis and enthesitis, conditions stereotypical of human inflammato
24 of PsA: peripheral arthritis, axial disease, enthesitis, dactylitis, and skin and nail psoriasis; add
25 rthritis (OR = 9.61), psoriasis (OR = 1.48), enthesitis/enthesopathy (OR = 12.65), and iridocyclitis
26 and 48 of 82 patients (59%) with peripheral enthesitis had PsA after 10 years compared with 37 of 30
27 ht of diagnostic difficulties with detecting enthesitis in clinical examinations and laboratory inves
28 in associated inflammatory features, such as enthesitis in psoriatic arthritis and uveitis in ankylos
29 erosion in association with Achilles tendon enthesitis in SpA is anatomically uncoupled from bone fo
30 drawn attention to the ubiquitous nature of enthesitis in spondyloarthropathies, especially adjacent
31 n psoriasis and PsA including improvement in enthesitis in the peripheral skeleton but has failed to
32 ts associated with spondyloarthropathy is an enthesitis (inflammation at sites where ligaments, tendo
33 fashion; inflammation at tendon insertions (enthesitis); inflammatory eye disease (uveitis); psorias
35 , or joint capsules to bone, which is termed enthesitis, is a characteristic feature of spondyloarthr
36 resonance imaging studies also suggest that enthesitis lesions may be extensive, which could explain
38 tion of HLA-B27 with bone pathology in early enthesitis may have implications for a better understand
40 as, beyond synovitis, it often also involves enthesitis, peritendinitis, tenosynovitis, osteitis and
42 ever, in much of PsA with axial involvement, enthesitis primarily manifests in ligamentous soft tissu
43 arthritis (125 [33.0%] of 379 patients) and enthesitis-related arthritis (113 [29.8%] of 379) were m
44 initive rash (44%), a competing diagnosis of enthesitis-related arthritis (23%), family history of ps
45 e most common subtypes of arthritis included enthesitis-related arthritis (37 [67.3%]), spondyloarthr
46 tients with SpA and 5 patients with juvenile enthesitis-related arthritis (juvenile ERA); samples wer
47 children and 136 patients with JIA (28 with enthesitis-related arthritis [ERA], 42 with persistent o
48 IA, including oligoarthritis, polyarthritis, enthesitis-related arthritis and psoriatic arthritis.
51 age was abnormally high in all JIA subtypes (enthesitis-related arthritis was not assessed), most str
53 ligoarticular juvenile idiopathic arthritis, enthesitis-related arthritis, and juvenile psoriatic art
54 ligoarticular juvenile idiopathic arthritis, enthesitis-related arthritis, or juvenile psoriatic arth
55 plates was evident in adolescent humans with enthesitis-related arthritis, which could progress to AS
59 al assessment of psoriatic nail disease, and enthesitis (using the PsA-modified Maastricht Ankylosing