Search Results - "Yuge, Isamu"

Transplanted human amniotic epithelial cells express connexin 26 and NA-K-adenosine triphosphatase in the inner ear by YUGE, Isamu, TAKUMI, Yutaka, KOYABU, Kuni, HASHIMOTO, Shigenari, TAKMHIMA, Seiji, FUKUYAMA, Tetsuhiro, NIKAIDO, Toshio, USAMI, Shin-Ichi

“…Cochlear fibrocytes are the crucial component of the inner ear homeostasis and its defect by various causes; GJB2 (connexin [Cx] 26) mutation, for example,…”
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Intramucosal PCO2 measurement as a new monitoring method of free jejunal transfer following pharyngo-laryngo-esophagectomy by IMANISHI, Yorihisa, NAMEKI, Hideo, ISOBE, Kiyoshi, KANEDA, Toru, YAMASHITA, Daisuke, YUGE, Isamu, OKADA, Waichiro, NAMEKI, Ichirota, ARAKI, Yasutomo, SUZUKI, Takafumi

“…The choices for practical monitoring of free jejunal transfer have been quite limited because of its own characteristics, such as buried form, lack of skin…”
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Identification of 605ins46, a novel GJB2 mutation in a Japanese family by Yuge, Isamu, Ohtsuka, Akihiro, Matsunaga, Tatsuo, Usami, Shin-ichi

“…Connexin 26 gene ( GJB2) mutations are known to be responsible for a significant portion (30–80%) of autosomal recessive congenital severe to profound…”
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Assessment of hyperacusis with a newly produced Japanese version of the Khalfa hyperacusis questionnaire by Oishi, Naoki, Yamada, Hiroyuki, Kanzaki, Sho, Kurita, Akihiro, Takiguchi, Yoichiro, Yuge, Isamu, Asama, Yoji, Masuda, Masatsugu, Ogawa, Kaoru

“…Objectives: The purpose of this study was to determine the validity and reliability of a Japanese version of the Khalfa hyperacusis questionnaire (KHQ) and…”
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Evaluation of the quality of life in sudden deafness patients by HHIA (hearing Hatidicap Inventory) and questionnaire by Sato, Minako, Ogawa, Kaoru, Saito, Hideyuki, Yamashita, Daisuke, Yuge, Isamu, Masuda, Masatsugu, Okamoto, Yasuhide, Kurita, Akihiro

“…After treatments, several patients with sudden deafness (SD) continued to have symptoms, including hearing loss, tinnitus and dizziness. These unresolved…”
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Early-phase outcome of Tinnitus Retraining Therapy and comparison of sound therapy measures by Yuge, Isamu, Satou, Minako, Shinden, Seiichi, Saitou, Hideyuki, Okamoto, Yasuhide, Kurita, Akihiro, Ogawa, Kaoru

“…Tinnitus Retraining Therapy (TRT) consists of directive counseling and sound therapy. As sound therapy, patients are told to use the following competing…”
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GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation by OHTSUKA, Akihiro, YUGE, Isamu, KIMURA, Shinobu, NAMBA, Atsushi, ABE, Satoko, VAN LAER, Lut, VAN CAMP, Guy, USAMI, Shin-Ichi

“…Mutations in the GJB2 gene (connexin 26) are the major cause of autosomal recessive non-syndromic hearing impairment in many populations. In contrast to the…”
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Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease by Usami, Shin-ichi, Takahashi, Kentaro, Yuge, Isamu, Ohtsuka, Akihiro, Namba, Atsushi, Abe, Satoko, Fransen, Erik, Patthy, Laszlo, Otting, Gottfried, Van Camp, Guy

“…The COCH gene is the only gene identified in man that causes autosomal dominantly inherited hearing loss associated with vestibular dysfunction. The condition…”
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Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleovestibular dysfunction, but not of Meniere's disease by USAMI, Shin-Ichi, TAKAHASHI, Kentaro, YUGE, Isamu, OHTSUKA, Akihiro, NAMBA, Atsushi, ABE, Satoko, FRANSEN, Erik, PATTHY, Laszlo, OTTING, Gottfried, VAN CAMP, Guy

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Molecular diagnosis of deafness: impact of gene identification by Usami, Shin-ichi, Koda, Eiko, Tsukamoto, Koji, Otsuka, Akihiro, Yuge, Isamu, Asamura, Kenji, Abe, Satoko, Akita, Jiro, Namba, Atsushi

“…Recent progress in identifying genes responsible for hearing loss enables the ENT clinician to apply molecular diagnosis by genetic testing. This article…”
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