Works matching AU Sato, Kenichi


Results: 83
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    Clinical heterogeneity of α‐synuclein gene duplication in Parkinson's disease.

    Published in:
    Annals of Neurology, 2006, v. 59, n. 2, p. 298
    By:
    • Kenya Nishioka;
    • Shin Hayashi;
    • Matthew J. Farrer;
    • Andrew B. Singleton;
    • Hiroyo Yoshino;
    • Hisamasa Imai;
    • Toshiaki Kitami;
    • Kenichi Sato;
    • Ryu Kuroda;
    • Hiroyuki Tomiyama;
    • Koichi Mizoguchi;
    • Miho Murata;
    • Tatsushi Toda;
    • Issei Imoto;
    • Johji Inazawa;
    • Yoshikuni Mizuno;
    • Nobutaka Hattori
    Publication type:
    Article
    15

    Novel PINK1 mutations in early‐onset parkinsonism.

    Published in:
    Annals of Neurology, 2004, v. 56, n. 3, p. 424
    By:
    • Yasuko Hatano;
    • Yuanzhe Li;
    • Kenichi Sato;
    • Shuichi Asakawa;
    • Yasuhiro Yamamura;
    • Hiroyuki Tomiyama;
    • Hiroyo Yoshino;
    • Masato Asahina;
    • Susumu Kobayashi;
    • Sharon Hassin‐Baer;
    • Chin‐Song Lu;
    • Arlene R. Ng;
    • Raymond L. Rosales;
    • Nobuyoshi Shimizu;
    • Tatsushi Toda;
    • Yoshikuni Mizuno;
    • Nobutaka Hattori
    Publication type:
    Article
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    Homeostatic and pathogenic roles of GM3 ganglioside molecular species in TLR4 signaling in obesity.

    Published in:
    EMBO Journal, 2020, v. 39, n. 12, p. 1, doi. 10.15252/embj.2019101732
    By:
    • Kanoh, Hirotaka;
    • Nitta, Takahiro;
    • Go, Shinji;
    • Inamori, Kei‐ichiro;
    • Veillon, Lucas;
    • Nihei, Wataru;
    • Fujii, Mayu;
    • Kabayama, Kazuya;
    • Shimoyama, Atsushi;
    • Fukase, Koichi;
    • Ohto, Umeharu;
    • Shimizu, Toshiyuki;
    • Watanabe, Taku;
    • Shindo, Hiroki;
    • Aoki, Sorama;
    • Sato, Kenichi;
    • Nagasaki, Mika;
    • Yatomi, Yutaka;
    • Komura, Naoko;
    • Ando, Hiromune
    Publication type:
    Article
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    Risk factors for discontinuation of exclusive breast feeding within 1month: a retrospective cohort study in Japan.

    Published in:
    International Breastfeeding Journal, 2022, v. 17, n. 1, p. 1, doi. 10.1186/s13006-022-00449-w
    By:
    • Yasuda, Shun;
    • Fukuda, Toma;
    • Toba, Naoya;
    • Kamo, Norihito;
    • Imaizumi, Karin;
    • Yokochi, Midori;
    • Okawara, Tomoko;
    • Takano, Seiko;
    • Yoshida, Hideko;
    • Kobayashi, Nobuko;
    • Kudo, Shingo;
    • Miyazaki, Kyohei;
    • Hosoya, Mamiko;
    • Sato, Kenichi;
    • Takano, Kei;
    • Kanno, Aya;
    • Murata, Tsuyoshi;
    • Kyozuka, Hyo;
    • Yamaguchi, Akiko;
    • Ito, Fumihiro
    Publication type:
    Article
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    Familial Parkinsonism with digenic parkin and PINK1 mutations.

    Published in:
    Movement Disorders, 2008, v. 23, n. 10, p. 1461, doi. 10.1002/mds.22143
    By:
    • Funayama, Manabu;
    • Li, Yuanzhe;
    • Tsoi, Tak-Hong;
    • Lam, Ching-Wan;
    • Ohi, Takekazu;
    • Yazawa, Shogo;
    • Uyama, Eiichiro;
    • Djaldetti, Ruth;
    • Melamed, Eldad;
    • Yoshino, Hiroyo;
    • Imamichi, Yoko;
    • Takashima, Hiroshi;
    • Nishioka, Kenya;
    • Sato, Kenichi;
    • Tomiyama, Hiroyuki;
    • Kubo, Shin-Ichiro;
    • Mizuno, Yoshikuni;
    • Hattori, Nobutaka
    Publication type:
    Article
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    Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries.

    Published in:
    Movement Disorders, 2006, v. 21, n. 8, p. 1102, doi. 10.1002/mds.20886
    By:
    • Tomiyama, Hiroyuki;
    • Li, Yuanzhe;
    • Funayama, Manabu;
    • Hasegawa, Kazuko;
    • Yoshino, Hiroyo;
    • Kubo, Shin-Ichiro;
    • Sato, Kenichi;
    • Hattori, Tatsuya;
    • Lu, Chin-Song;
    • Inzelberg, Rivka;
    • Djaldetti, Ruth;
    • Melamed, Eldad;
    • Amouri, Rim;
    • Gouider-Khouja, Neziha;
    • Hentati, Faycal;
    • Hatano, Yasuko;
    • Wang, Mei;
    • Imamichi, Yoko;
    • Mizoguchi, Koichi;
    • Miyajima, Hiroaki
    Publication type:
    Article
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