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1 pathological decrease of the lubrication in degenerative joint disease.
2 arthritis (OA) is an age-related progressive degenerative joint disease.
3 an turnover and cartilage degradation during degenerative joint disease.
4 whereby CSA may be an effective therapy for degenerative joint disease.
5 ut not in successfully treated infections or degenerative joint disease.
6 d function, and may serve as an indicator of degenerative joint disease.
7 short stature, joint laxity and early-onset degenerative joint disease.
8 avoiding the evolution of this condition to degenerative joint disease.
9 score was also significantly associated with degenerative joint disease.
10 Osteoarthritis (OA) is the most common degenerative joint disease.
11 Osteoarthritis is a complex degenerative joint disease.
12 e sarcopenia, cardiovascular remodeling, and degenerative joint disease.
13 of SnCs as a therapeutic target for treating degenerative joint disease.
14 the catabolic phenotype may protect against degenerative joint disease.
15 0 could modulate cartilage mineralization in degenerative joint diseases.
16 age is an early event in the pathogenesis of degenerative joint diseases.
17 resolved associated comorbidities were 6/14 degenerative joint disease, 9/10 gastroesophageal reflux
21 al phenotype in which surviving mice acquire degenerative joint diseases and tumors in multiple organ
23 Importantly, we observe no clinical signs of degenerative joint disease apart from mild, or in one ca
24 ltrating immune cells play a central role in degenerative joint disease associated with osteoarthriti
25 matory drug (NSAID) robenacoxib in cats with degenerative joint disease-associated pain (DJD-pain).
28 bular joint (TMJ) disc displacement (DD) and degenerative joint disease (DJD) has never been conclusi
29 intelligence (AI) model for the screening of degenerative joint disease (DJD) using temporomandibular
30 th and without reduction (DDwR and DDwoR) to degenerative joint disease (DJD), and patient-reported o
32 esity comorbidity in these patients included degenerative joint disease, gastroesophageal reflux dise
36 eritance, coalitions also can be acquired by degenerative joint disease, inflammatory arthritis, infe
38 n of Smad3 exon 8 (Smad3(ex8/ex8)) developed degenerative joint disease resembling human osteoarthrit
39 ifferentiation and results in development of degenerative joint disease resembling osteoarthritis in
40 Osteoarthritis (OA) is the most prevalent degenerative joint disease, resulting in joint pain, imp
45 y in the local treatment of inflammatory and degenerative joint disease, such as osteoarthritis and r
47 rome, hypertension, gastroesophageal reflux, degenerative joint disease symptoms, type 2 diabetes mel
52 a, hypoventilation, gastroesophageal reflux, degenerative joint disease, urinary incontinence, venous
54 teoarthritis (OA) is the most common chronic degenerative joint disease which causes substantial join
56 omologous recombination leads to early onset degenerative joint disease, which is revealed by simulta
58 steoarthritis (OA) is a prevalent, heritable degenerative joint disease with a substantial public hea