Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Tohru Futami"'
Autor:
Kenichi Fukiage, Makoto Watanabe, Shiro Ikegawa, Zheng Wang, Cantas Alev, Yoshihiro Yamanaka, Jing-Yi Xue, Megumi Nishio, Yann Pretemer, Junya Toguchida, Shunsuke Kawai, Tohru Futami, Masako Tsukanaka, Sanae Nagata, Sakura Tamaki
Publikováno v:
Stem Cell Reports
Summary Chondrodysplasias are hereditary diseases caused by mutations in the components of growth cartilage. Although the unfolded protein response (UPR) has been identified as a key disease mechanism in mouse models, no suitable in vitro system has
Autor:
Kenichi Fukiage, Jing-Yi Xue, Masako Tsukanaka, Yann Pretemer, Tohru Futami, Junya Toguchida, Shunsuke Kawai, Zheng Wang, Megumi Nishio, Cantas Alev, Sanae Nagata, Makoto Watanabe, Shiro Ikegawa, Sakura Tamaki
SummaryChondrodysplasias are hereditary diseases caused by mutations in the components of growth cartilage. Although the unfolded protein response (UPR) has been identified as a key disease mechanism in mouse models, no suitablein vitrosystem has bee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91cc7c5b698493439987117a3bbeae9e
https://doi.org/10.1101/2020.05.19.103960
https://doi.org/10.1101/2020.05.19.103960
Publikováno v:
Journal of Pediatric Orthopaedics B. 26:519-525
The aim of this study is to evaluate the complications of humeral lengthening and their associated factors. Fifty-four achondroplastic patients were treated by bilateral humeral lengthening. Our original shoulder sling was sufficient to prevent shoul
Autor:
Shinichi Satsuma, Takashi Saisu, Takuya Otani, Atsushi Kita, Yasuhiko Kawaguchi, Toshio Kitano, Tohru Futami
Publikováno v:
Journal of Orthopaedic Science. 21:847-851
Background Treatment for unstable slipped capital femoral epiphysis (SCFE) is challenging and controversial. For many years, the debate centered around closed treatments and especially the pros and cons of manual reduction and its concrete procedure.
Publikováno v:
Journal of Children's Orthopaedics
Purpose The aim of this study was to first develop and use 1.0 s ultrafast magnetic resonance imaging (MRI) to confirm the location of the femoral head in non-sedated infants with developmental dysplasia of the hip (DDH) after reduction with spica ca
Publikováno v:
Clinical Pediatric Endocrinology. 25:103-106
Gain-of-function mutations in the fibroblast growth factor receptor 3 gene (FGFR3) result in a group of skeletal dysplasias, such as prototypic achondroplasia (ACH: OMIM #100800) and lethal thanatophoric dysplasia (TD1: OMIM #187600). Hypochondroplas
Autor:
Shunsuke Fujibayashi, Tomiharu Matsushita, Takeshi Sakamoto, Kiyoyuki Sasaki, Shuich Matsuda, Mitsuru Takemoto, Eigo Ota, Toshiyuki Kawai, Hiroaki Kimura, Takashi Nakamura, Bungo Otsuki, Tohru Futami, Masashi Neo
Publikováno v:
European Spine Journal. 25:1698-1705
Image-based navigational patient-specific templates (PSTs) for pedicle screw (PS) placement have been described. With recent advances in three-dimensional computer-aided designs and additive manufacturing technology, various PST designs have been rep
Publikováno v:
Modern Rheumatology. 27:1098-1100
Chronic infantile neurological, cutaneous, and articular (CINCA) syndrome is a systemic autoinflammatory disease caused by increased production of interleukin (IL)-1β. We present a case of CINCA syndrome followed up to skeletal maturity. Joint contr
Publikováno v:
Journal of pediatric orthopedics. Part B. 24(4)
The aims of this study were to quantify the femoral head volume (FHV) in developmental dysplasia of the hip (DDH) and to estimate its relation with the severity of the disease. Fifty-one patients (age range 2-11 months) with unilateral DDH were evalu
Publikováno v:
Journal of Pediatric Orthopaedics, Part B. 10:298-303
Thirty-three images using magnetic resonance imaging (MRI) in 10 patients with slipped capital femoral epiphysis were evaluated. The MRI of affected hips delineated typical widening of the physis. Sequential MRI demonstrated the process of premature