Detailed clinical features and genotype–phenotype correlation in an OTOF-related hearing loss cohort in Japan von Iwasa, Yoh-ichiro, Nishio, Shin-ya, Yoshimura, Hidekane, Sugaya, Akiko, Kataoka, Yuko, Maeda, Yukihide, Kanda, Yukihiko, Nagai, Kyoko, Naito, Yasushi, Yamazaki, Hiroshi, Ikezono, Tetsuo, Matsuda, Han, Nakai, Masako, Tona, Risa, Sakurai, Yuika, Motegi, Remi, Takeda, Hidehiko, Kobayashi, Marina, Kihara, Chiharu, Ishino, Takashi, Morita, Shin-ya, Iwasaki, Satoshi, Takahashi, Masahiro, Furutate, Sakiko, Oka, Shin-ichiro, Kubota, Toshinori, Arai, Yasuhiro, Kobayashi, Yumiko, Kikuchi, Daisuke, Shintani, Tomoko, Ogasawara, Noriko, Honkura, Yohei, Izumi, Shuji, Hyogo, Misako, Ninoyu, Yuzuru, Suematsu, Mayumi, Nakayama, Jun, Tsuchihashi, Nana, Okami, Mayuri, Sakata, Hideaki, Yoshihashi, Hiroshi, Kobayashi, Taisuke, Kumakawa, Kozo, Yoshida, Tadao, Esaki, Tomoko, Usami, Shin-ichi

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Frequency and clinical features of hearing loss caused by STRC deletions von Yokota, Yoh, Moteki, Hideaki, Nishio, Shin-ya, Yamaguchi, Tomomi, Wakui, Keiko, Kobayashi, Yumiko, Ohyama, Kenji, Miyazaki, Hiromitsu, Matsuoka, Rina, Abe, Satoko, Kumakawa, Kozo, Takahashi, Masahiro, Sakaguchi, Hirofumi, Uehara, Natsumi, Ishino, Takashi, Kosho, Tomoki, Fukushima, Yoshimitsu, Usami, Shin-ichi

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Correction to: Detailed clinical features and genotype–phenotype correlation in an OTOF-related hearing loss cohort in Japan von Iwasa, Yoh-ichiro, Nishio, Shin-ya, Yoshimura, Hidekane, Sugaya, Akiko, Kataoka, Yuko, Maeda, Yukihide, Kanda, Yukihiko, Nagai, Kyoko, Naito, Yasushi, Yamazaki, Hiroshi, Ikezono, Tetsuo, Matsuda, Han, Nakai, Masako, Tona, Risa, Sakurai, Yuika, Motegi, Remi, Takeda, Hidehiko, Kobayashi, Marina, Kihara, Chiharu, Ishino, Takashi, Morita, Shin-ya, Iwasaki, Satoshi, Takahashi, Masahiro, Furutate, Sakiko, Oka, Shin-ichiro, Kubota, Toshinori, Arai, Yasuhiro, Kobayashi, Yumiko, Kikuchi, Daisuke, Shintani, Tomoko, Ogasawara, Noriko, Honkura, Yohei, Izumi, Shuji, Hyogo, Misako, Ninoyu, Yuzuru, Suematsu, Mayumi, Nakayama, Jun, Tsuchihashi, Nana, Okami, Mayuri, Sakata, Hideaki, Yoshihashi, Hiroshi, Kobayashi, Taisuke, Kumakawa, Kozo, Yoshida, Tadao, Esaki, Tomoko, 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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A randomized controlled clinical trial of topical insulin-like growth factor-1 therapy for sudden deafness refractory to systemic corticosteroid treatment von Nakagawa, Takayuki, Kumakawa, Kozo, Usami, Shin-ichi, Hato, Naohito, Tabuchi, Keiji, Takahashi, Mariko, Fujiwara, Keizo, Sasaki, Akira, Komune, Shizuo, Sakamoto, Tatsunori, Hiraumi, Harukazu, Yamamoto, Norio, Tanaka, Shiro, Tada, Harue, Yamamoto, Michio, Yonezawa, Atsushi, Ito-Ihara, Toshiko, Ikeda, Takafumi, Shimizu, Akira, Tabata, Yasuhiko, Ito, Juichi

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POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing l... von Kitano, Tomohiro, Miyagawa, Maiko, Nishio, Shin-Ya, Moteki, Hideaki, Oda, Kiyoshi, Ohyama, Kenji, Miyazaki, Hiromitsu, Hidaka, Hiroshi, Nakamura, Ken-Ichi, Murata, Takaaki, Matsuoka, Rina, Ohta, Yoko, Nishiyama, Nobuhiro, Kumakawa, Kozo, Furutate, Sakiko, Iwasaki, Satoshi, Yamada, Takechiyo, Ohta, Yumi, Uehara, Natsumi, Noguchi, Yoshihiro, Usami, Shin-Ichi

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Successful cochlear implantation in a patient with Epstein syndrome during long-term follow-up von Mori, Anjin, Takeda, Hidehiko, Kobayashi, Marina, Misawa, Takeru, Watanabe, Ryoko, Abe, Satoko, Kumakawa, Kozo, Nishio, Shinya, Usami, Shinichi, Yamasoba, Tatsuya

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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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Prognostic impact of salvage treatment on hearing recovery in patients with sudden sensorineural hearing loss refractory to systemic corticosteroids: A retrospective observational... von Nakagawa, Takayuki, Yamamoto, Michio, Kumakawa, Kozo, Usami, Shin-ichi, Hato, Naohito, Tabuchi, Keiji, Takahashi, Mariko, Fujiwara, Keizo, Sasaki, Akira, Komune, Shizuo, Yamamoto, Norio, Hiraumi, Harukazu, Sakamoto, Tatsunori, Shimizu, Akira, Ito, Juichi

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OTOF mutation screening in Japanese severe to profound recessive hearing loss patients von Iwasa, Yoh-ichiro, Nishio, Shin-ya, Yoshimura, Hidekane, Kanda, Yukihiko, Kumakawa, Kozo, Abe, Satoko, Naito, Yasushi, Nagai, Kyoko, Usami, Shin-ichi

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Facial nerve stimulation following cochlear implantation for X-linked stapes gusher syndrome leading to identification of a novel POU3F4 mutation von Wester, Jacob L., MD, Merna, Catherine, BS, Peng, Kevin A., MD, Lewis, Rebecca, AuD, Sepahdari, Ali R., MD, Ishiyama, Gail, MD, Hosokawa, Kumino, MD, Kumakawa, Kozo, MD, Ishiyama, Akira, MD

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Frequency of Usher syndrome type 1 in deaf children by massively parallel DNA sequencing von Yoshimura, Hidekane, Miyagawa, Maiko, Kumakawa, Kozo, Nishio, Shin-Ya, Usami, Shin-Ichi

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Auditory Brainstem Implantation Improves Speech Recognition in Neurofibromatosis Type II Patients von Matthies, Cordula, Brill, Stefan, Kaga, Kimitaka, Morita, Akio, Kumakawa, Kozo, Skarzynski, Henryk, Claassen, Andre, Hui, Yau, Chiong, Charlotte, Müller, Joachim, Behr, Robert

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Discrimination of Japanese monosyllables in patients with high-frequency hearing loss von Karino, Shotaro, Usami, Shin-ichi, Kumakawa, Kozo, Takahashi, Haruo, Tono, Tetsuya, Naito, Yasushi, Doi, Katsumi, Ito, Ken, Suzuki, Mitsuya, Sakata, Hideaki, Takumi, Yutaka, Iwasaki, Satoshi, Kakigi, Akinobu, Yamasoba, Tatsuya

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Small fenestra stapedotomy saving the stapedial tendon von Kumakawa, Kozo

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Massively Parallel DNA Sequencing Successfully Identified Seven Families With Deafness-Associated MYO6 Mutations: The Mutational Spectrum and Clinical Characteristics von Miyagawa, Maiko, Nishio, Shin-ya, Kumakawa, Kozo, Usami, Shin-ichi

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Development of oral communication in hearing-impaired children who could be observed for a long term ―Comparison between groups with moderate/severe hearing impairment and the grou... von Sato, Kiyoko, Sugiuchi, Tomoko, Shiromoto, Osamu, Sugio, Yuichiro, Kumakawa, Kozo

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Round Window Application of an Active Middle Ear Implant: A Comparison With Hearing Aid Usage in Japan von Iwasaki, Satoshi, Usami, Shin-ichi, Takahashi, Haruo, Kanda, Yukihiko, Tono, Tetsuya, Doi, Katsumi, Kumakawa, Kozo, Gyo, Kiyofumi, Naito, Yasushi, Kanzaki, Sho, Yamanaka, Noboru, Kaga, Kimitaka

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Detailed Clinical Features of IPTPRQ/I-Associated Hearing Loss Identified in a Large Japanese Hearing Loss Cohort von Sakuma, Naoko, Nishio, Shin-ya, Goto, Shin-ichi, Honkura, Yohei, Oda, Kiyoshi, Takeda, Hidehiko, Kobayashi, Marina, Kumakawa, Kozo, Iwasaki, Satoshi, Takahashi, Masahiro, Ito, Taku, Arai, Yasuhiro, Isono, Yasuhiro, Obara, Natsuko, Matsunobu, Takeshi, Okubo, Kimihiro, Usami, Shin-ichi

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