Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Seiji Tsuji"'
Autor:
Kazuyuki Hirao, Kohji Nagashima, Marco A. Condoretty, Seiji Tsuji, Hideki Kawasaki, Heidy Visbal, Luz Quispe, Hitomi Miki
Publikováno v:
Journal of the Ceramic Society of Japan. 123:38-42
Publikováno v:
Orthopedics & Traumatology. 61:245-248
Publikováno v:
Orthopedics & Traumatology. 59:506-509
Publikováno v:
Orthopedics & Traumatology. 58:634-638
【目的】成人における上腕骨顆上骨折の手術療法では早期可動域訓練を可能とする強固な固定が必要とされる.今回この骨折に対しプレート固定を行った症例の治療成績について検討し
Publikováno v:
Orthopedics & Traumatology. 57:548-552
術前にレントゲン上で計測した骨頭サイズと術中に計測した骨頭サイズとが大きく異なった症例を経験した.これを避けるため,計測用の金属性リングを用いる方法を採用し,精度を上
Publikováno v:
Orthopedics & Traumatology. 60:634-636
Autor:
Akio K. Inoue, Hiroshi Hashimoto, Setsuro Komiya, Tetsuya Hamada, Seiji Tsuji, Michihisa Zenmyo, Koji Hiraoka, Kensei Nagata
Publikováno v:
Spine. 26:310-313
STUDY DESIGN A case report. OBJECTIVES To illustrate a rare case of synovial sarcoma arising within a peripheral nerve. SUMMARY OF BACKGROUND DATA A synovial sarcoma arising within a peripheral nerve is very unusual. Only five cases of primary synovi
Autor:
Masanori Hisaoka, Hiroshi Hashimoto, Setsuro Komiya, Seiji Tsuji, Yosuke Morimitsu, Toshitaka Nakamura, Shohei Shimajiri, Masahiro Ushijima
Publikováno v:
The American Journal of Pathology. 153:1807-1812
The reciprocal translocation t(X;18)(p11;q11) is known to be highly characteristic of synovial sarcoma, and its consequence, an SYT-SSX fusion gene, is expected to be a diagnostic molecular marker. In this study, we conducted a reverse transcription-
Autor:
Y Kaneko, H Eguchi, Hiroshi Hashimoto, Masanori Hisaoka, Yosuke Morimitsu, A Jimi, J Watanabe, Seiji Tsuji
Publikováno v:
Histopathology. 33:369-374
Aims We report two unusual cases of intrapulmonary small round cell tumour with evidence that they are primitive neuroectodermal tumours. Methods and results The patients were a 25-year-old woman and a 15-year-old man, in whom mass shadows were found
Publikováno v:
Virchows Archiv. 433:323-329
Fibrosarcomatous (FS) change in a rare, but well-known phenomenon encountered in dermatofibrosarcoma protuberans (DFSP), and an increased chance in an adverse outcome has been suggested in patients with DFSP having FS areas (DFSP-FS). As altered p53