Výsledky vyhledávání - Mawatari, Go

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  1. 1
    Base Curve of Progressive Addition Lenses Influences Clear Vision and Stereopsis Area

    Base Curve of Progressive Addition Lenses Influences Clear Vision and Stereopsis Area Autor Mawatari, Go, Uchida, Saeko, Nao-i, Nobuhisa

    Vydáno 2020
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  2. 2
    Modified Muscle Transposition Procedure for a Case of Inferior Rectus Muscle Aplasia

    Modified Muscle Transposition Procedure for a Case of Inferior Rectus Muscle Aplasia Autor Makino, Shinji, Hozawa, Kozue, Kondo, Reiko, Kanai, Mika, Suto, Haruko, Mawatari, Go, Ito, Kanako

    Vydáno 2014
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  3. 3
    Genetic and Phenotypic Landscape of PRPH2-Associated Retinal Dystrophy in Japan

    Genetic and Phenotypic Landscape of PRPH2-Associated Retinal Dystrophy in Japan Autor Oishi, Akio, Fujinami, Kaoru, Mawatari, Go, Naoi, Nobuhisa, Ikeda, Yasuhiro, Ueno, Shinji, Kuniyoshi, Kazuki, Hayashi, Takaaki, Kondo, Hiroyuki, Mizota, Atsushi, Shinoda, Kei, Kusuhara, Sentaro, Nakamura, Makoto, Iwata, Takeshi, Tsujikawa, Akitaka, Tsunoda, Kazushige

    Vydáno 2021
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  4. 4
    Clinical and genetic characteristics of 14 patients from 13 Japanese families with RPGR-associated retinal disorder: report of eight novel variants

    Clinical and genetic characteristics of 14 patients from 13 Japanese families with RPGR-associated retinal disorder: report of eight novel variants Autor Mawatari, Go, Fujinami, Kaoru, Liu, Xiao, Yang, Lizhu, Yokokawa, Yu-Fujinami, Komori, Shiori, Ueno, Shinji, Terasaki, Hiroko, Katagiri, Satoshi, Hayashi, Takaaki, Kuniyoshi, Kazuki, Miyake, Yozo, Tsunoda, Kazushige, Yoshitake, Kazutoshi, Iwata, Takeshi, Nao-i, Nobuhisa

    Vydáno 2019
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  5. 5
    Correction to: Clinical and genetic characteristics of 14 patients from 13 Japanese families with RPGR-associated retinal disorder: report of eight novel variants

    Correction to: Clinical and genetic characteristics of 14 patients from 13 Japanese families with RPGR-associated retinal disorder: report of eight novel variants Autor Mawatari, Go, Fujinami, Kaoru, Liu, Xiao, Yang, Lizhu, Fujinami-Yokokawa, Yu, Komori, Shiori, Ueno, Shinji, Terasaki, Hiroko, Katagiri, Satoshi, Hayashi, Takaaki, Kuniyoshi, Kazuki, Miyake, Yozo, Tsunoda, Kazushige, Yoshitake, Kazutoshi, Iwata, Takeshi, Nao-i, Nobuhisa

    Vydáno 2020
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  6. 6
    Genetic Spectrum of EYS-associated Retinal Disease in a Large Japanese Cohort: Identification of Disease-associated Variants with Relatively High Allele Frequency

    Genetic Spectrum of EYS-associated Retinal Disease in a Large Japanese Cohort: Identification of Disease-associated Variants with Relatively High Allele Frequency Autor Yang, Lizhu, Fujinami, Kaoru, Ueno, Shinji, Kuniyoshi, Kazuki, Hayashi, Takaaki, Kondo, Mineo, Mizota, Atsushi, Naoi, Nobuhisa, Shinoda, Kei, Kameya, Shuhei, Fujinami-Yokokawa, Yu, Liu, Xiao, Arno, Gavin, Pontikos, Nikolas, Kominami, Taro, Terasaki, Hiroko, Sakuramoto, Hiroyuki, Katagiri, Satoshi, Mizobuchi, Kei, Nakamura, Natsuko, Mawatari, Go, Kurihara, Toshihide, Tsubota, Kazuo, Miyake, Yozo, Yoshitake, Kazutoshi, Iwata, Takeshi, Tsunoda, Kazushige

    Vydáno 2020
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