Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Yumeta Shimazu"'
Autor:
Ryo, Miyata, Masatsugu, Hamaji, Akiyoshi, Nakakura, Satoshi, Morita, Yumeta, Shimazu, Masashi, Ishikawa, Hidenao, Kayawake, Toshi, Menju, Yasuto, Sakaguchi, Makoto, Sonobe, Mamoru, Takahashi, Akihiro, Aoyama, Ryota, Sumitomo, Cheng-Long, Huang, Tomoya, Kono, Ryo, Miyahara, Akira, Matsumoto, Hiromichi, Katakura, Takahisa, Fukada, Hiroaki, Sakai, Masashi, Kobayashi, Norihito, Okumura, Naoki, Date, Takuji, Fujinaga, Ei, Miyamoto, Tatsuo, Nakagawa, Hiroshi, Date
Publikováno v:
Surgery Today. 53:135-144
The effect of postoperative tegafur-uracil on overall survival (OS) after resection of stage I adenocarcinoma has been shown in clinical trials. The purpose of this study was to investigate whether findings from randomized trials of adjuvant tegafur-
Autor:
Ryo Miyata, Masatsugu Hamaji, Atsushi Kawaguchi, Yumeta Shimazu, Masaki Ikeda, Masashi Ishikawa, Hidenao Kayawake, Toshi Menju, Masashi Kobayashi, Norihito Okumura, Yasuto Sakaguchi, Makoto Sonobe, Akira Matsumoto, Tsuyoshi Shoji, Hiromichi Katakura, Ryota Sumitomo, Cheng-Long Huang, Mamoru Takahashi, Akihiro Aoyama, Yusuke Muranishi, Tomoya Kono, Ryo Miyahara, Naoki Date, Takuji Fujinaga, Ei Miyamoto, Tatsuo Nakagawa, Takahisa Fukada, Hiroaki Sakai, Hiroshi Date
Publikováno v:
European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery. 62(5)
OBJECTIVES The aim of this study was to analyse the long-term survival outcomes and prognostic factors of patients receiving epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) as first-line treatment for postoperative recurrent E
Publikováno v:
Kyobu geka. The Japanese journal of thoracic surgery. 72(9)
Morvan syndrome is a rare autoimmune neurological disease characterized by peripheral nerve hyperexcitability, autonomic dysfunction and encephalopathy. Morvan syndrome is often associated with thymoma as a paraneoplastic condition. Here we present a
Publikováno v:
Journal of Surgical Case Reports
Malignant triton tumor (MTT) is a rare subtype of malignant peripheral nerve sheath tumors with rhabdomyoblastic differentiation. Although the condition may manifest sporadically, it typically affects adult patients with neurofibromatosis type 1. In
Autor:
Tomomi, Isono, Hiroyoshi, Watanabe, Yumeta, Shimazu, Nobuhisa, Yamazaki, Hirokazu, Tanaka, Masaharu, Nakade
Publikováno v:
Kyobu geka. The Japanese journal of thoracic surgery. 70(6)
A 71-years-old man, who had undergone resection for sacral chordoma 15 years before, was admitted to our hospital to treat a nodule in the right middle lobe detected by computed tomography. The nodule was resected and was histologically diagnosed as