TMC1 and TMC2 Are Components of the Mechanotransduction Channel in Hair Cells of the Mammalian Inner Ear von Pan, Bifeng, Géléoc, Gwenaelle S., Asai, Yukako, Horwitz, Geoffrey C., Kurima, Kiyoto, Ishikawa, Kotaro, Kawashima, Yoshiyuki, Griffith, Andrew J., Holt, Jeffrey R.

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Autoimmune hemolytic anemia associated with Takenouchi–Kosaki syndrome von Ishikawa, Kotaro, Uchiyama, Toru, Kaname, Tadashi, Kawai, Toshinao, Ishiguro, Akira

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Splenectomy as an effective treatment for macrothrombocytopenia in Takenouchi-Kosaki syndrome von Yamano, Shio, Iguchi, Akihiro, Ishikawa, Kotaro, Sakamoto, Atsushi, Uchiyama, Toru, Yanagi, Kumiko, Kaname, Tadashi, Kunishima, Shinji, Ishiguro, Akira

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WFS1 mutation screening in a large series of Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis von Kobayashi, Masafumi, Miyagawa, Maiko, Nishio, Shin-Ya, Moteki, Hideaki, Fujikawa, Taro, Ohyama, Kenji, Sakaguchi, Hirofumi, Miyanohara, Ikuyo, Sugaya, Akiko, Naito, Yasushi, Morita, Shin-Ya, Kanda, Yukihiko, Takahashi, Masahiro, Ishikawa, Kotaro, Nagano, Yuki, Tono, Tetsuya, Oshikawa, Chie, Kihara, Chiharu, Takahashi, Haruo, Noguchi, Yoshihiro, Usami, Shin-Ichi

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Comprehensive analysis of syndromic hearing loss patients in Japan von Ideura, Michie, Nishio, Shin-ya, Moteki, Hideaki, Takumi, Yutaka, Miyagawa, Maiko, Sato, Teruyuki, Kobayashi, Yumiko, Ohyama, Kenji, Oda, Kiyoshi, Matsui, Takamichi, Ito, Tsukasa, Suzumura, Hiroshi, Nagai, Kyoko, Izumi, Shuji, Nishiyama, Nobuhiro, Komori, Manabu, Kumakawa, Kozo, Takeda, Hidehiko, Kishimoto, Yoko, Iwasaki, Satoshi, Furutate, Sakiko, Ishikawa, Kotaro, Fujioka, Masato, Nakanishi, Hiroshi, Nakayama, Jun, Horie, Rie, Ohta, Yumi, Naito, Yasushi, Kakudo, Mariko, Sakaguchi, Hirofumi, Kataoka, Yuko, Sugahara, Kazuma, Hato, Naohito, Nakagawa, Takashi, Tsuchihashi, Nana, Kanda, Yukihiko, Kihara, Chiharu, Tono, Tetsuya, Miyanohara, Ikuyo, Ganaha, Akira, Usami, Shin-ichi

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Comprehensive genetic screening of KCNQ4 in a large autosomal dominant nonsyndromic hearing loss cohort: genotype-phenotype correlations and a founder mutation von Naito, Takehiko, Nishio, Shin-ya, Iwasa, Yoh-ichiro, Yano, Takuya, Kumakawa, Kozo, Abe, Satoko, Ishikawa, Kotaro, Kojima, Hiromi, Namba, Atsushi, Oshikawa, Chie, Usami, Shin-ichi

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Massively parallel DNA sequencing facilitates diagnosis of patients with Usher syndrome type 1 von Yoshimura, Hidekane, Iwasaki, Satoshi, Nishio, Shin-Ya, Kumakawa, Kozo, Tono, Tetsuya, Kobayashi, Yumiko, Sato, Hiroaki, Nagai, Kyoko, Ishikawa, Kotaro, Ikezono, Tetsuo, Naito, Yasushi, Fukushima, Kunihiro, Oshikawa, Chie, Kimitsuki, Takashi, Nakanishi, Hiroshi, Usami, Shin-Ichi

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The Prevalence and Clinical Characteristics of TECTA -Associated Autosomal Dominant Hearing Loss von Yasukawa, Rika, Moteki, Hideaki, Nishio, Shin-Ya, Ishikawa, Kotaro, Abe, Satoko, Honkura, Yohei, Hyogo, Misako, Mihashi, Ryota, Ikezono, Tetsuo, Shintani, Tomoko, Ogasawara, Noriko, Shirai, Kyoko, Yoshihashi, Hiroshi, Ishino, Takashi, Otsuki, Koshi, Ito, Tsukasa, Sugahara, Kazuma, Usami, Shin-Ichi

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Public Assistance for Persons with Hearing Loss von Ishikawa, Kotaro

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Disruption of fibroblast growth factor receptor 3 signaling results in defects in cellular differentiation, neuronal patterning, and hearing impairment von Puligilla, Chandrakala, Feng, Feng, Ishikawa, Kotaro, Bertuzzi, Stefano, Dabdoub, Alain, Griffith, Andrew J., Fritzsch, Bernd, Kelley, Matthew W.

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Metallurgical study on erosion and corrosion behaviors of steels exposed to liquid lead–bismuth flow von Kondo, Masatoshi, Takahashi, Minoru, Suzuki, Tadashi, Ishikawa, Kotaro, Hata, Koji, Qiu, Suizheng, Sekimoto, Hiroshi

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Are patients with severe epistaxis caused by hereditary hemorrhagic telangiectasia satisfied with nostril closure surgery? von Ichimura, Keiichi, Kikuchi, Hisashi, Imayoshi, Shoichiro, Yamauchi, Tomohiko, Ishikawa, Kotaro

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Oral administration of acidic xylooligosaccharides prevents the development of atopic dermatitis-like skin lesions in NC/Nga mice von Ohbuchi, T., Oji Paper Co. Ltd., Tokyo (Japan), Sakaino, M, Takahashi, T, Azumi, N, Ishikawa, K, Kawazoe, S, Kobayashi, Y, Kido, Y

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Guidelines for the evaluation of hearing aid fitting (2010) von Kodera, Kazuoki, Hosoi, Hiroshi, Okamoto, Makito, Manabe, Toshiki, Kanda, Yukihiko, Shiraishi, Kimio, Sugiuchi, Tomoko, Suzuki, Keiko, Tauchi, Hikaru, Nishimura, Tadashi, Matsuhira, Toshimasa, Ishikawa, Kotaro

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Phenotype of DFNA11: A Nonsyndromic Hearing Loss Caused by a Myosin VIIA Mutation von Tamagawa, Yuya, Ishikawa, Kazuhiro, Ishikawa, Kotaro, Ishida, Takashi, Kitamura, Ken, Makino, Shinji, Tsuru, Tadahiko, Ichimura, Keiichi

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プレドニゾロンにより結核を発症したELISPOT判定保留の自己免疫性肝炎の1例 von 石川, 孝太郎, 木村, 修, 生形, 晃男, 川邉, 誠, 大方, 英樹, 平本, 圭一郎, 阿曽沼, 祥, 梅村, 賢, 佐藤, 晃彦, 下瀬川, 徹

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The prevalence and clinical features of MYO7A-related hearing loss including DFNA11, DFNB2 and USH1B von Watanabe, Kizuki, Nishio, Shin-ya, Usami, Shin-ichi

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Nonsyndromic Hearing Loss Caused by a Mitochondrial T7511C Mutation von Ishikawa, Kotaro, Tamagawa, Yuya, Takahashi, Katsumasa, Kimura, Hiroshi, Kusakari, Jun, Hara, Akira, Ichimura, Keiichi

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Mutation spectrum and genotype-phenotype correlation of hearing loss patients caused by SLC26A4 mutations in the Japanese: a large cohort study von Miyagawa, Maiko, Nishio, Shin-Ya, Usami, Shin-Ichi

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Effects of age on survival and morbidity in gastric cancer patients undergoing gastrectomy von Fujiwara, Yoshinori, Fukuda, Shuichi, Tsujie, Masanori, Ishikawa, Hajime, Kitani, Kotaro, Inoue, Keisuke, Yukawa, Masao, Inoue, Masatoshi

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