Результати пошуку - Kazuhiro Muramatsu

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  1. 1
    Effects of a selective inhibitor of cyclic AMP phosphodiesterase on the pial microcirculation in feline cerebral ischemia.

    Effects of a selective inhibitor of cyclic AMP phosphodiesterase on the pial microcirculation in feline cerebral ischemia. за авторством K. Tanaka, Fumio Gotoh, Yasuo Fukuuchi, Takahiro Amano, Daisuke Uematsu, Jun Kawamura, Takemori Yamawaki, Nobuhiko Itoh, K Obara, Kazuhiro Muramatsu

    Опубліковано 1989
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  2. 2
    Clinical features and varieties of non-motor fluctuations in Parkinson's disease: A Japanese multicenter study

    Clinical features and varieties of non-motor fluctuations in Parkinson's disease: A Japanese multicenter study за авторством Morinobu Seki, Kazushi Takahashi, Daisuke Uematsu, Ban Mihara, Yoko Morita, Kazuo Isozumi, Kouichi Ohta, Kazuhiro Muramatsu, Toshitaka Shirai, Shigeru Nogawa, Jun Gotoh, Keiji Yamaguchi, Yutaka Tomita, Daisuke Yasutomi, Yoshihiro Nihei, Satoko Iwasawa, Norihiro Suzuki

    Опубліковано 2012
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  3. 3
    Severe pediatric acute encephalopathy syndromes related to SARS-CoV-2

    Severe pediatric acute encephalopathy syndromes related to SARS-CoV-2 за авторством Hiroshi Sakuma, Jun‐ichi Takanashi, Kazuhiro Muramatsu, H. Kondo, Takashi Shiihara, Motomasa Suzuki, Kazuo Okanari, Mariko Kasai, Osamu Mitani, Tomoyuki Nakazawa, Taku Omata, Konomi Shimoda, Yuichi Abe, Yoshihiro Maegaki, Kei Murayama, Yuka Murofushi, Hiroaki Nagase, Akihisa Okumura, Yasunari Sakai, Hiroko Tada, Masashi Mizuguchi

    Опубліковано 2023
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  4. 4
    Molecular genetic analysis of 30 families with Joubert syndrome

    Molecular genetic analysis of 30 families with Joubert syndrome за авторством Toshifumi Suzuki, Noriko Miyake, Yoshinori Tsurusaki, Nobuhiko Okamoto, A. Alkindy, A. Inaba, Masashi Sato, Shuichi Ito, Kazuhiro Muramatsu, S. Kimura, Daisuke Ieda, Shinji Saitoh, Meire Ioshie Hiyane, Hiroshi Suzumura, Kazuma Yagyu, Hideaki Shiraishi, Masatoshi Nakajima, Noboru Fueki, Y. Habata, Yuki Ueda, Yumiko Komatsu, Kunimasa Yan, Konomi Shimoda, Yoshinori Shitara, Seiji Mizuno, Kenji Ichinomiya, Koichi Sameshima, Yu Tsuyusaki, K. KUROSAWA, Yasunari Sakai, Kazuhiro Haginoya, Yukio Kobayashi, C. Yoshizawa, M. Hisano, Mitsuko Nakashima, Hirotomo Saitsu, Satoru Takeda, Naomichi Matsumoto

    Опубліковано 2016
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  5. 5
    Structural variant allelic heterogeneity in MECP2 duplication syndrome provides insight into clinical severity and variability of disease expression

    Structural variant allelic heterogeneity in MECP2 duplication syndrome provides insight into clinical severity and variability of disease expression за авторством Davut Pehli̇van, Jesse D. Bengtsson, Sameer S. Bajikar, Christopher M. Grochowski, Ming Yin Lun, Mira Gandhi, Angad Jolly, Alexander J. Trostle, Holly K. Harris, Bernhard Suter, Sukru Aras, Melissa B. Ramocki, Haowei Du, Michele G. Mehaffey, KyungHee Park, Ellen Wilkey, Cemal Karakas, Jesper Eisfeldt, Maria Pettersson, Lynn Liu, Marwan Shinawi, Virginia Kimonis, Wojciech Wiszniewski, Kyle McKenzie, Timo Roser, Angela Maria Vianna‐Morgante, Alberto S. Cornier, Ahmed Abdelmoity, James Paul Hwang, Shalini N. Jhangiani, Donna M. Muzny, Tadahiro Mitani, Kazuhiro Muramatsu, Shin Nabatame, Daniel G. Glaze, Jawid M. Fatih, Richard A. Gibbs, Zhandong Liu, Anna Lindstrand, Fritz J. Sedlazeck, James R. Lupski, Huda Y. Zoghbi, Claudia M.B. Carvalho

    Опубліковано 2024
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  6. 6
    Clinical characteristics of SARS-CoV-2-associated encephalopathy in children: Nationwide epidemiological study

    Clinical characteristics of SARS-CoV-2-associated encephalopathy in children: Nationwide epidemiological study за авторством Mariko Kasai, Hiroshi Sakuma, Yuichi Abe, Ichiro Kuki, Yoshihiro Maegaki, Kei Murayama, Yuka Murofushi, Hiroaki Nagase, Masahiro Nishiyama, Akihisa Okumura, Yasunari Sakai, Hiroko Tada, Masashi Mizuguchi, Jun‐ichi Takanashi, Satoshi Akamine, Pin Fee Chong, Tatsuya Ema, Sayaka Enomoto, Ryohei Fukatsu, Yoshiyuki Hanaoka, Ayuko Igarashi, Tae Ikeda, Kouhei Ishida, Nobutsune Ishikawa, Shinji Itamura, Hideyuki Iwayama, Nanako Kawata, Go Kawano, Kenjiro Kikuchi, Osamu Kobayashi, H. Kondo, Seigo Korematsu, Tsuyoshi Matsuoka, Yuki Minamisawa, Osamu Mitani, Kanako Mizuma, Tatsuo Mori, Shinichiro Morıchı, Yoko Moriyama, Mitsuo Motobayashi, Hirotaka Motoi, Kazuhiro Muramatsu, Kazuyuki Nakamura, Tomoyuki Nakazawa, Yutaka Negishi, Yuka Nishizawa, Hiroshi Okada, Kazuo Okanari, Keisuke Oki, Yoshinori Okumura, Taku Omata, Saki Saeki, Fumikazu Sano, Kentaro Sano, Tatsuharu Sato, Takashi Shiihara, Konomi Shimoda, Motomasa Suzuki, Ryuta Tanaka, Chiho Tokorodani, Mitsugu Uematsu, Hiroyuki Yamada, Naohiro Yamamoto, Tatsuya Yamamoto, Haruna Yokoyama

    Опубліковано 2024
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  7. 7
    Biallelic mutations in the 3′ exonuclease TOE1 cause pontocerebellar hypoplasia and uncover a role in snRNA processing

    Biallelic mutations in the 3′ exonuclease TOE1 cause pontocerebellar hypoplasia and uncover a role in snRNA processing за авторством Rea M. Lardelli, Ashleigh E. Schaffer, Veerle Rc Eggens, Maha S. Zaki, Stephanie Grainger, Shashank Sathe, Eric L. Van Nostrand, Zinayida Schlachetzki, Başak Rosti, Naiara Akizu, Eric Scott, Jennifer L. Silhavy, Laura D. Heckman, Rasim Özgür Rosti, Esra Dikoglu, Anne Gregor, Alicia Guemez‐Gamboa, Damir Musaev, Rohit Mande, Ari Widjaja, Timothy Shaw, Sebastian Markmiller, Isaac Marin‐Valencia, Justin H. Davies, Linda De Meırleır, Hülya Kayserili, Umut Altunoğlu, Mary Louise Freckmann, Linda Warwick, David Chitayat, Susan Blasér, Ahmet Okay Çağlayan, Kaya Bilgüvar, Hüseyin Per, Christina Fagerberg, Henrik Thybo Christesen, Maria Kibæk, Kimberly A. Aldinger, David K. Manchester, Naomichi Matsumoto, Kazuhiro Muramatsu, Hirotomo Saitsu, Masaaki Shiina, Kazuhiro Ogata, Nicola Foulds, William B. Dobyns, C. Neil, David Traver, Luigina Spaccini, Stefania Maria Bova, Stacey B. Gabriel, Murat Günel, Enza Maria Valente, Marie‐Cécile Nassogne, Eric J. Bennett, G Yeo, Frank Baas, Jens Lykke‐Andersen, Joseph G. Gleeson

    Опубліковано 2017
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  8. 8
    Genetic and clinical landscape of childhood cerebellar hypoplasia and atrophy

    Genetic and clinical landscape of childhood cerebellar hypoplasia and atrophy за авторством Masamune Sakamoto, Kazuhiro Iwama, Masayuki Sasaki, Akihiko Ishiyama, Hirofumi Komaki, Takashi Saito, Eri Takeshita, Yuko Shimizu‐Motohashi, Kazuhiro Haginoya, Tomoko Kobayashi, Tomohide Goto, Yu Tsuyusaki, Mizue Iai, Kenji Kurosawa, Hitoshi Osaka, Jun Tohyama, Yu Kobayashi, Nobuhiko Okamoto, Yume Suzuki, Satoko Kumada, Kenji Inoue, Hideaki Mashimo, Atsuko Arisaka, Ichiro Kuki, Harumi Saijo, Kenji Yokochi, Mitsuhiro Kato, Yuji Inaba, Yuko Gomi, Shinji Saitoh, Kentaro Shirai, Masafumi Morimoto, Yuishin Izumi, Yoriko Watanabe, Shin-Ichiro Nagamitsu, Yasunari Sakai, Shinobu Fukumura, Kazuhiro Muramatsu, Tomomi Ogata, Keitaro Yamada, Keiko Ishigaki, Kyoko Hirasawa, Konomi Shimoda, Manami Akasaka, Kosuke Kohashi, Takafumi Sakakibara, Masashi Ikuno, Noriko Sugino, Takahiro Yonekawa, Semra Gürsoy, Tayfun Çinleti, Chong Ae Kim, Keng Wee Teik, Chan Mei Yan, Muzhirah Haniffa, Chihiro Ohba, Shuuichi Ito, Hirotomo Saitsu, Ken Saida, Naomi Tsuchida, Yuri Uchiyama, Eriko Koshimizu, Atsushi Fujita, Kohei Hamanaka, Kazuharu Misawa, Satoko Miyatake, Takeshi Mizuguchi, Noriko Miyake, Naomichi Matsumoto

    Опубліковано 2022
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