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1 n syndrome, are characterized by generalized joint hypermobility.
2 d connective tissue abnormalities, including joint hypermobility.
3 rs that have the orthopedic manifestation of joint hypermobility.
4 ene may account for some subgroups of benign joint hypermobility.
5 ) is characterized by an association between joint hypermobility and musculoskeletal pains, the latte
9 s provide hope that more common varieties of joint hypermobility can be understood and that effective
10 ctive tissue/myopathy overlap disorders with joint hypermobility, contractures, mild skeletal dysplas
12 underlie classic Ehlers-Danlos syndrome, and joint hypermobility is an important clinical manifestati
14 onnective tissue, manifesting as early-onset joint hypermobility, joint contractures, muscle weakness
17 vely inherited form of EDS (characterized by joint hypermobility, skin hyperextensibility, and cardia
20 tional families, one of which diagnosed with joint hypermobility syndrome/Ehlers-Danlos syndrome hype
21 and body mass index-adjusted heritability of joint hypermobility was estimated to be 70% (95% confide
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