コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 of a mechanosensor in sensory neurons causes joint contracture.
2 channels to developmental malformations and joint contractures.
3 easily eroded skin, rocker bottom feet, and joint contractures.
4 thin, flexed digits, crumpled ears and mild joint contractures.
5 y characterized by early childhood onset and joint contractures.
6 sorders that are characterized by congenital joint contractures.
7 to skeletal deformities in conjunction with joint contractures.
8 the latter is additionally characterized by joint contractures.
10 acterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxi
11 , a childhood-onset disease characterized by joint contractures and in some cases by abnormalities of
12 haracterized by progressive muscle weakness, joint contractures and respiratory insufficiency, to Bet
16 a classic CCA phenotype with arachnodactyly, joint contractures, and abnormal pinnae, whereas her dau
17 l therapy, bracing, soft tissue releases for joint contractures, and early stabilization of the spine
22 ment in hand function, inflammatory indices, joint contractures, arthritis signs, overall functional
25 tions are short stature, a high incidence of joint contractures at birth and progressive scoliosis an
26 and include developmental delay, hypotonia, joint contractures, behavioral abnormalities, Marfanoid
27 cal investigations confirmed sclerotic skin, joint contractures, bone abnormalities, alopecia, and gr
29 characterised by delayed speech development, joint contractures, dysmorphic features and dysmotility
30 yndrome characterized by multiple congenital joint contractures, frequently is caused by lesions in t
32 dhood onset autosomal dominant myopathy with joint contractures, has recently been localized to 21q i
34 steady improvement of skin changes and knee joint contractures in patients with stage 5 chronic kidn
35 ey result in considerable morbidity owing to joint contracture, loss of flexibility, and disfiguremen
36 e recently reported to cause "JMP" syndrome (joint contractures, muscle atrophy, microcytic anemia, a
37 e autoinflammatory syndrome characterized by joint contractures, muscle atrophy, microcytic anemia, a
38 ifesting as early-onset joint hypermobility, joint contractures, muscle weakness and bone dysplasia a
40 ure and/or toxicity of therapy; for example, joint contractures or joint damage may result in life-lo
42 cGVHD, particularly if sclerodermatous skin, joint contractures, or oral manifestations are present.
43 g germline NFATC2 variant and presented with joint contractures, osteochondromas, and recurrent B-cel
45 t baseline (P = 0.0078) and changes in large joint contractures (P = 0.0072), tender joint counts (P
46 e suffering from severe muscle weakness with joint contractures, pronounced growth retardation and ky
47 opmental condition characterized by multiple joint contractures resulting from reduced or absent feta
48 eudohypertrophy of calf muscles, progressive joint contractures, severe scoliosis, elevated serum cre
50 l illnesses including disuse muscle atrophy, joint contractures, thromboembolic disease, and insulin
51 ined when cutaneous sclerosis, fasciitis, or joint contracture was first documented in the medical re
54 c silhouette on radiograph (P = 0.04), large joint contractures (wrist, elbow, knee) (P = 0.008), and