Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Kiyoshi Oda"'
Autor:
Naoko Sakuma, Shin-ya Nishio, Shin-ichi Goto, Yohei Honkura, Kiyoshi Oda, Hidehiko Takeda, Marina Kobayashi, Kozo Kumakawa, Satoshi Iwasaki, Masahiro Takahashi, Taku Ito, Yasuhiro Arai, Yasuhiro Isono, Natsuko Obara, Takeshi Matsunobu, Kimihiro Okubo, Shin-ichi Usami
Publikováno v:
Genes, Vol 15, Iss 4, p 489 (2024)
The PTPRQ gene has been identified as one of the genes responsible for non-syndromic sensorineural hearing loss (SNHL), and assigned as DFNA73 and DFNB84. To date, about 30 causative PTPRQ variants have been reported to cause SNHL. However, the detai
Externí odkaz:
https://doaj.org/article/b0c01e38a5644460a5ff2f20c0e6e309
Autor:
Michie Ideura, Shin-ya Nishio, Hideaki Moteki, Yutaka Takumi, Maiko Miyagawa, Teruyuki Sato, Yumiko Kobayashi, Kenji Ohyama, Kiyoshi Oda, Takamichi Matsui, Tsukasa Ito, Hiroshi Suzumura, Kyoko Nagai, Shuji Izumi, Nobuhiro Nishiyama, Manabu Komori, Kozo Kumakawa, Hidehiko Takeda, Yoko Kishimoto, Satoshi Iwasaki, Sakiko Furutate, Kotaro Ishikawa, Masato Fujioka, Hiroshi Nakanishi, Jun Nakayama, Rie Horie, Yumi Ohta, Yasushi Naito, Mariko Kakudo, Hirofumi Sakaguchi, Yuko Kataoka, Kazuma Sugahara, Naohito Hato, Takashi Nakagawa, Nana Tsuchihashi, Yukihiko Kanda, Chiharu Kihara, Tetsuya Tono, Ikuyo Miyanohara, Akira Ganaha, Shin-ichi Usami
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-13 (2019)
Abstract More than 400 syndromes associated with hearing loss and other symptoms have been described, corresponding to 30% of cases of hereditary hearing loss. In this study we aimed to clarify the mutation spectrum of syndromic hearing loss patients
Externí odkaz:
https://doaj.org/article/96252fd9eecb4e0fb430b805ec9cf43d
Autor:
Tomohiro Kitano, Maiko Miyagawa, Shin-Ya Nishio, Hideaki Moteki, Kiyoshi Oda, Kenji Ohyama, Hiromitsu Miyazaki, Hiroshi Hidaka, Ken-Ichi Nakamura, Takaaki Murata, Rina Matsuoka, Yoko Ohta, Nobuhiro Nishiyama, Kozo Kumakawa, Sakiko Furutate, Satoshi Iwasaki, Takechiyo Yamada, Yumi Ohta, Natsumi Uehara, Yoshihiro Noguchi, Shin-Ichi Usami
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0177636 (2017)
A variant in a transcription factor gene, POU4F3, is responsible for autosomal dominant nonsyndromic hereditary hearing loss, DFNA15. To date, 14 variants, including a whole deletion of POU4F3, have been reported to cause HL in various ethnic groups.
Externí odkaz:
https://doaj.org/article/1f0880387c96479eac09fb7838185e0b
Publikováno v:
Nippon Jibiinkoka Gakkai Kaiho. 124:1013-1020
Autor:
Hiroshi Hidaka, Kiyoshi Oda, Toshimitsu Kobayashi, Hiroki Yamamoto, Ryoukichi Ikeda, Naohiro Yoshida
Publikováno v:
Otologyneurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology. 41(3)
Objective To describe a case of traumatic pneumolabyrinth and subsequent hearing recovery after ejection of air with transcanal endoscopic surgical exploration. Patients A 38-year-old man was struck by his child while cleaning his ear with an ear pic
Autor:
Yoshihiko Esu, Eri Takahashi, Hiromi Kanazawa, Masayo Hasegawa, Satoshi Tamii, Mariya Masuda, Naohiro Yoshida, Hiroki Yamamoto, Kiyoshi Oda, Akihiro Shinnabe
Publikováno v:
Nippon Jibiinkoka Gakkai Kaiho. 121:783-790
Autor:
Kiyoshi Oda, Risako Kakuta, Mihoko Irimada, Yukio Katori, Ryoukichi Ikeda, Kazuhiro Nomura, Daiki Ozawa, Shunsuke Takai, Kenji Ohyama
Publikováno v:
Ear, Nose & Throat Journal. :014556132110264
Background: Ventilation tube (VT) insertion is the most common treatment for otitis media with effusion (OME). However, OME recurrence and persistent tympanic membrane (TM) perforation after VT removal are encountered in a certain percentage of such
Autor:
Yukio Katori, Kiyoshi Oda, Takashi Takahashi, Hiroshi Hidaka, Mihoko Irimada, Kazuaki Arai, Risako Kakuta, Daiki Ozawa, Hisakazu Yano, Hiromitsu Miyazaki, Mitsuo Kaku
Publikováno v:
The Tohoku Journal of Experimental Medicine. 232:301-304
Streptococcus (S.) pyogenes is well recognized as the most common pathogen causing pharyngotonsillitis in school-age children. In Japan, mucoid Streptococcus pneumoniae is well known as a causative agent of severe acute otitis media (AOM); however, m
Autor:
Kiyoshi Oda, Hiroki Yamamoto, Toshimitsu Kobayashi, Hiroshi Hidaka, Ryoukichi Ikeda, Naohiro Yoshida, Oda, Kiyoshi, Yamamoto, Hiroki, Kobayashi, Toshimitsu, Hidaka, Hiroshi, Ikeda, Ryoukichi, Yoshida, Naohiro
Publikováno v:
Otology & Neurotology; Mar2020, Vol. 41 Issue 3, p359-363, 5p
Autor:
Toshimitsu Kobayashi, Makiko Miyazaki, Kiyoshi Oda, Ayako Nakanome, Takayuki Kudo, Syun Sagaii, Masaru Tateda
Publikováno v:
JOURNAL OF JAPAN SOCIETY FOR HEAD AND NECK SURGERY. 16:97-102