Works by Kano, Hiroki

Results: 29
    1

    Combined Therapy with Ixazomib, Lenalidomide, and Dexamethasone for Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Gammopathy, and Skin Changes Syndrome.

    Published in:
    Internal Medicine, 2022, v. 61, n. 17, p. 2567, doi. 10.2169/internalmedicine.8786-21
    By:
    • Tomoki Suichi;
    • Sonoko Misawa;
    • Yukari Sekiguchi;
    • Kazumoto Shibuya;
    • Keigo Nakamura;
    • Hiroki Kano;
    • Yuya Aotsuka;
    • Ryo Otani;
    • Morooka, Marie;
    • Shokichi Tsukamoto;
    • Yusuke Takeda;
    • Naoya Mimura;
    • Chikako Ohwada;
    • Emiko Sakaida;
    • Satoshi Kuwabara
    Publication type:
    Article
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    Fukuyama-type congenital muscular dystrophy (FCMD) and α-dystroglycanopathy.

    Published in:
    Congenital Anomalies, 2003, v. 43, n. 2, p. 97, doi. 10.1111/j.1741-4520.2003.tb01033.x
    By:
    • Toda, Tatsushi;
    • Kobayashi, Kazuhiro;
    • Takeda, Satoshi;
    • Sasaki, Junko;
    • Kurahashi, Hiroki;
    • Kano, Hiroki;
    • Tachikawa, Masaji;
    • Wang, Fan;
    • Nagai, Yoshitaka;
    • Taniguchi, Kiyomi;
    • Taniguchi, Mariko;
    • Sunada, Yoshihide;
    • Terashima, Toshio;
    • Endo, Tamao;
    • Matsumura, Kiichiro
    Publication type:
    Article
    5

    Molecular pathogenesis of Spondylocheirodysplastic Ehlers-Danlos syndrome caused by mutant ZIP13 proteins.

    Published in:
    EMBO Molecular Medicine, 2014, v. 6, n. 8, p. 1028, doi. 10.15252/emmm.201303809
    By:
    • Bin, Bum‐Ho;
    • Hojyo, Shintaro;
    • Hosaka, Toshiaki;
    • Bhin, Jinhyuk;
    • Kano, Hiroki;
    • Miyai, Tomohiro;
    • Ikeda, Mariko;
    • Kimura‐Someya, Tomomi;
    • Shirouzu, Mikako;
    • Cho, Eun‐Gyung;
    • Fukue, Kazuhisa;
    • Kambe, Taiho;
    • Ohashi, Wakana;
    • Kim, Kyu‐Han;
    • Seo, Juyeon;
    • Choi, Dong‐Hwa;
    • Nam, Yeon‐Ju;
    • Hwang, Daehee;
    • Fukunaka, Ayako;
    • Fujitani, Yoshio
    Publication type:
    Article
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    Fukuyama-type congenital muscular dystrophy (FCMD) and oc-dystroglycanopathy.

    Published in:
    Clinical Genetics, 1993, v. 43, n. 2, p. 97, doi. 10.1111/j.1399-0004.1993.tb04427.x
    By:
    • Toda, Tatsushi;
    • Kobayashi, Kazuhiro;
    • Takeda, Satoshi;
    • Sasaki, Junko;
    • Kurahashi, Hiroki;
    • Kano, Hiroki;
    • Tachikawa, Masaji;
    • Wang, Fan;
    • Nagai, Yoshitaka;
    • Taniguchi, Kiyomi;
    • Taniguchi, Mariko;
    • Sunada, Yoshihide;
    • Terashima, Toshio;
    • Endo, Tamao;
    • Matsumura, Kiichiro
    Publication type:
    Article
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    Decreased initial compound muscle action potential amplitudes in myasthenia gravis.

    Published in:
    Neurology & Clinical Neuroscience, 2022, v. 10, n. 5, p. 245, doi. 10.1111/ncn3.12661
    By:
    • Kojima, Yuta;
    • Shibuya, Kazumoto;
    • Uzawa, Akiyuki;
    • Kano, Hiroki;
    • Nakamura, Keigo;
    • Yasuda, Manato;
    • Suzuki, Yo‐ichi;
    • Tsuneyama, Atsuko;
    • Suichi, Tomoki;
    • Ozawa, Yukiko;
    • Misawa, Sonoko;
    • Noto, Yu‐ichi;
    • Mizuno, Toshiki;
    • Kuwabara, Satoshi
    Publication type:
    Article
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    L1 retrotransposition can occur early in human embryonic development.

    Published in:
    Human Molecular Genetics, 2007, v. 16, n. 13, p. 1587, doi. 10.1093/hmg/ddm108
    By:
    • van den Hurk, José A.J.M.;
    • Meij, Iwan C.;
    • del Carmen Seleme, Maria;
    • Kano, Hiroki;
    • Nikopoulos, Konstantinos;
    • Hoefsloot, Lies H.;
    • Sistermans, Erik A.;
    • de Wijs, Ilse J.;
    • Mukhopadhyay, Arijit;
    • Plomp, Astrid S.;
    • de Jong, Paulus T.V.M.;
    • Kazazian, Haig H.;
    • Cremers, Frans P.M.
    Publication type:
    Article
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    Fukutin is required for maintenance of muscle integrity, cortical histiogenesis and normal eye development.

    Published in:
    Human Molecular Genetics, 2003, v. 12, n. 12, p. 1449, doi. 10.1093/hmg/ddg153
    By:
    • Takeda, Satoshi;
    • Kondo, Mari;
    • Sasaki, Junko;
    • Kurahashi, Hiroki;
    • Kano, Hiroki;
    • Arai, Ken;
    • Misaki, Kazuyo;
    • Fukui, Takehiko;
    • Kobayashi, Kazuhiro;
    • Tachikawa, Masaji;
    • Imamura, Michihiro;
    • Nakamura, Yusuke;
    • Shimizu, Teruo;
    • Murakami, Tatsufumi;
    • Sunada, Yoshihide;
    • Fujikado, Takashi;
    • Matsumura, Kiichiro;
    • Terashima, Toshio;
    • Toda, Tatsushi
    Publication type:
    Article
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    Diagnostic utility of Gold Coast criteria for amyotrophic lateral sclerosis in Asia.

    Published in:
    Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2024, v. 25, n. 3/4, p. 264, doi. 10.1080/21678421.2024.2303062
    By:
    • Otani, Ryo;
    • Shibuya, Kazumoto;
    • Shimizu, Toshio;
    • Kitaoji, Takamasa;
    • Noto, Yu-Ichi;
    • Bokuda, Kota;
    • Kimura, Hideki;
    • Suichi, Tomoki;
    • Nakamura, Keigo;
    • Kano, Hiroki;
    • Morooka, Marie;
    • Aotsuka, Yuya;
    • Ogushi, Moeko;
    • Misawa, Sonoko;
    • Kuwabara, Satoshi
    Publication type:
    Article
    28

    Japanese founder duplications/triplications involving BHLHA9 are associated with split-hand/ foot malformation with or without long bone deficiency and Gollop-Wolfgang complex

    Published in:
    Orphanet Journal of Rare Diseases, 2014, v. 9, n. 1, p. 125, doi. 10.1186/s13023-014-0125-5
    By:
    • Eiko Nagata;
    • Hiroki Kano;
    • Fumiko Kato;
    • Rie Yamaguchi;
    • Shinichi Nakashima;
    • Shinichiro Takayama;
    • Rika Kosaki;
    • Hidefumi Tonoki;
    • Seiji Mizuno;
    • Satoshi Watanabe;
    • Koh-ichiro Yoshiura;
    • Tomoki Kosho;
    • Tomonobu Hasegawa;
    • Mamori Kimizuka;
    • Atsushi Suzuki;
    • Kenji Shimizu;
    • Hirofumi Ohashi;
    • Nobuhiko Haga;
    • Hironao Numabe;
    • Emiko Horii
    Publication type:
    Article
    29

    Japanese founder duplications/triplications involving BHLHA9 are associated with split-hand/foot malformation with or without long bone deficiency and Gollop-Wolfgang complex.

    Published in:
    2014
    By:
    • Nagata, Eiko;
    • Kano, Hiroki;
    • Kato, Fumiko;
    • Yamaguchi, Rie;
    • Nakashima, Shinichi;
    • Takayama, Shinichiro;
    • Kosaki, Rika;
    • Tonoki, Hidefumi;
    • Mizuno, Seiji;
    • Watanabe, Satoshi;
    • Yoshiura, Koh-Ichiro;
    • Kosho, Tomoki;
    • Hasegawa, Tomonobu;
    • Kimizuka, Mamori;
    • Suzuki, Atsushi;
    • Shimizu, Kenji;
    • Ohashi, Hirofumi;
    • Haga, Nobuhiko;
    • Numabe, Hironao;
    • Horii, Emiko
    Publication type:
    journal article