Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Makoto Sakoh"'
Autor:
Yukiko Motohashi, Chitose Murata, Kazuya Oyanagi, Makoto Sakoh, Takashi Hitosugi, Hirofumi Murase
Publikováno v:
Japanese Journal of Oral & Maxillofacial Surgery. 52:77-80
Adult rhabdomyoma is rare benign tumor of muscle origin usually occurring in the head and neck region. Only a few cases of this disease have been reported in the literature.We describe a 63-year-old man with an adult rhabdomyoma arising in the floor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::420b82f64d09627249d9899c066ffe0c
https://doi.org/10.5794/jjoms.52.77
https://doi.org/10.5794/jjoms.52.77
Autor:
Chitose Murata, Naoyuki Sato, Hirofumi Murase, Makoto Sakoh, Takeshi Hitosugi, Yukiko Motohashi
Publikováno v:
Japanese Journal of Oral & Maxillofacial Surgery. 50:616-619
Multiple myeloma is a disease characterized by the proliferation of tumorigenically transformed plasma cells in bone marrow. It is associated with various symptoms. We describe a patient who was given a diagnosis of multiple myeloma based on the resu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8df7b251758c4433b5cf260fc9bae6f3
https://doi.org/10.5794/jjoms.50.616
https://doi.org/10.5794/jjoms.50.616
Autor:
Makoto Sakoh
Publikováno v:
Japanese Journal of Oral & Maxillofacial Surgery. 37:763-778
We sometimes perform the operation of the palate on the diabetic patients. The present study, therefore, investigates the wound healing of the palate in mice with diabetes and with diabetes injected with insulin.Methods and Results:Experiment I (Pala
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f546a699e210d644b855ddacb5157d3
https://doi.org/10.5794/jjoms.37.763
https://doi.org/10.5794/jjoms.37.763
Autor:
Kazuo Shimozato, Tadashi Yamamoto, Yuji Kamiya, Yoichiro Kameyama, Kana Tokura, Makoto Sakoh, Takashi Yasue, Shigeki Takehana, Hijiri Mori, Tsuyoshi Kawai
Publikováno v:
Japanese Journal of Oral & Maxillofacial Surgery. 36:2074-2082
Basal cell nevus syndrome is primarily considered to be an autosomal dominant hereditary disease frequently accompanying basal cell epitheliomas, multiple jaw cysts, anomalies of the rib, palmar and plantar pits, calcification of the cerebro-falx, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bcdcc38710c4690bfb96d68db5502935
https://doi.org/10.5794/jjoms.36.2074
https://doi.org/10.5794/jjoms.36.2074
Autor:
Makoto Sakoh, Hideki Ogiuchi, Megumi Chino, Hiroyuki Kaneko, Kenji Fukada, Tatsuo Takahashi, Akira Takaishi, Hiroaki Kataumi
Publikováno v:
Japanese Journal of Oral & Maxillofacial Surgery. 42:1215-1217
A pigmented nevus is defined as a hamartomatous proliferation of nevus cells. It is a very common skin lesion. Pigmented nevi of the oral mucosa are considered a rare lesion and only a few cases have been reported in Japan.We recently encountered 2 c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1b9d912192360207d32154cb906a53f
https://doi.org/10.5794/jjoms.42.1215
https://doi.org/10.5794/jjoms.42.1215