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1 to 10 of 25 literature results
Multiple center study to evaluate cerebrospinal fluid (CSF) concentrations of nitric oxide metabolites [NOx] in relation to neurologic severity and pr…
Authors: Shinji Kimura, Noboru Hosaka, Itaru Yuge, Akiyoshi Yamazaki, Kohta Suda, Hiroshi Taneichi, Hiroshi Denda, Naoto Endo
Source: Spine. 2009 Aug 15
View Full TextCochlear fibrocytes are the crucial component of the inner ear homeostasis and its defect by various causes; GJB2 (connexin [Cx] 26) mutation, for exa…
Authors: Isamu Yuge, Yutaka Takumi, Kuni Koyabu, Shigenari Hashimoto, Seiji Takashima, Tetsuhiro Fukuyama, Toshio Nikaido, Shin-ichi Usami
Source: Transplantation. 2004 May 15
View Full TextMutations in the GJB2 gene (connexin 26) are the major cause of autosomal recessive non-syndromic hearing impairment in many populations. In contrast …
Authors: Akihiro Ohtsuka, Isamu Yuge, Shinobu Kimura, Atsushi Namba, Satoko Abe, Lut Van Laer, Guy Van Camp, Shin-ichi Usami
Source: Human genetics. 2003 Apr
View Full TextThe choices for practical monitoring of free jejunal transfer have been quite limited because of its own characteristics, such as buried form, lack of…
Authors: Yorihisa Imanishi, Hideo Nameki, Kiyoshi Isobe, Toru Kaneda, Daisuke Yamashita, Isamu Yuge, Waichiro Okada, Ichirota Nameki, Yasutomo Araki, Takafumi Suzuki
Source: Plastic and reconstructive surgery. 2003 Oct
View Full TextAfter treatments, several patients with sudden deafness (SD) continued to have symptoms, including hearing loss, tinnitus and dizziness. These unresol…
Authors: Minako Sato, Kaoru Ogawa, Hideyuki Saito, Daisuke Yamashita, Isamu Yuge, Masatsugu Masuda, Yasuhide Okamoto, Akihiro Kurita
Source: Nihon Jibiinkoka Gakkai kaiho. 2005 Dec
View Full TextConnexin 26 gene (GJB2) mutations are known to be responsible for a significant portion (30-80%) of autosomal recessive congenital severe to profound …
Authors: Isamu Yuge, Akihiro Ohtsuka, Tatsuo Matsunaga, Shin-ichi Usami
Source: Auris, nasus, larynx. 2002 Oct
View Full TextThe COCH gene is the only gene identified in man that causes autosomal dominantly inherited hearing loss associated with vestibular dysfunction. The c…
Authors: Shin-ichi Usami, Kentaro Takahashi, Isamu Yuge, Akihiro Ohtsuka, Atsushi Namba, Satoko Abe, Erik Fransen, Laszlo Patthy, Gottfried Otting, Guy Van Camp
Source: European journal of human genetics : EJHG. 2003 Oct
View Full TextThe case report presented herein shows tortuosity of the vertebral artery in a patient with cervical myelopathy. This case led the authors to evaluate…
Authors: M Oga, I Yuge, K Terada, A Shimizu, Y Sugioka
Source: Spine. 1996 May 1
View Full TextRecent progress in identifying genes responsible for hearing loss enables the ENT clinician to apply molecular diagnosis by genetic testing. This arti…
Authors: Shin-ichi Usami, Eiko Koda, Koji Tsukamoto, Akihiro Otsuka, Isamu Yuge, Kenji Asamura, Satoko Abe, Jiro Akita, Atsushi Namba
Source: Audiology & neuro-otology. 2002 May-Jun
View Full TextWe herein report the case of a 68-year-old man with diabetes who developed pyogenic arthritis of a lumbar facet joint after spinal injection. We perfo…
Authors: K Okazaki, K Sasaki, S Matsuda, I Yuge, K Omiya, H Kido, H Ueda
Source: American journal of orthopedics (Belle Mead, N.J.). 2000 Mar
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