Hasil Pencarian - Hiroyuki Ishiura

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  1. 1
    JASPAC: Japan Spastic Paraplegia Research Consortium

    JASPAC: Japan Spastic Paraplegia Research Consortium oleh Kishin Koh, Hiroyuki Ishiura, Shoji Tsuji, Yoshihisa Takiyama

    Diterbitkan 2018-08-01
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  2. 2
    SPG9A with the new occurrence of an ALDH18A1 mutation in a CMT1A family with PMP22 duplication: case report

    SPG9A with the new occurrence of an ALDH18A1 mutation in a CMT1A family with PMP22 duplication: case report oleh Kishin Koh, Ryusuke Takaki, Hiroyuki Ishiura, Shoji Tsuji, Yoshihisa Takiyama

    Diterbitkan 2021-02-01
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  3. 3
    Neurofilament light chain levels in cerebrospinal fluid as a sensitive biomarker for cerebral adrenoleukodystrophy

    Neurofilament light chain levels in cerebrospinal fluid as a sensitive biomarker for cerebral adrenoleukodystrophy oleh Toshiyuki Kakumoto, Takashi Matsukawa, Hiroyuki Ishiura, Harushi Mori, Shoji Tsuji, Tatsushi Toda

    Diterbitkan 2023-07-01
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  4. 4
    A novel mutation in the GBA2 gene in a Japanese patient with SPG46: A case report

    A novel mutation in the GBA2 gene in a Japanese patient with SPG46: A case report oleh Keiko Nakamura-Shindo, Kenjiro Ono, Kishin Koh, Hiroyuki Ishiura, Shoji Tsuji, Yoshihisa Takiyama, Masahito Yamada

    Diterbitkan 2020-06-01
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  5. 5
    VPS13D‐related disorders presenting as a pure and complicated form of hereditary spastic paraplegia

    VPS13D‐related disorders presenting as a pure and complicated form of hereditary spastic paraplegia oleh Kishin Koh, Hiroyuki Ishiura, Haruo Shimazaki, Michiko Tsutsumiuchi, Yuta Ichinose, Haitian Nan, Shun Hamada, Toshihisa Ohtsuka, Shoji Tsuji, Yoshihisa Takiyama

    Diterbitkan 2020-03-01
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  6. 6
    Family with congenital contractural arachnodactyly due to a novel multiexon deletion of the FBN2 gene

    Family with congenital contractural arachnodactyly due to a novel multiexon deletion of the FBN2 gene oleh Hiroki Yagi, Hiroshi Takiguchi, Norifumi Takeda, Ryo Inuzuka, Yuki Taniguchi, Kristine Joyce Porto, Hiroyuki Ishiura, Jun Mitsui, Hiroyuki Morita, Issei Komuro

    Diterbitkan 2022-02-01
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  7. 7
    The novel de novo mutation of KIF1A gene as the cause for Spastic paraplegia 30 in a Japanese case

    The novel de novo mutation of KIF1A gene as the cause for Spastic paraplegia 30 in a Japanese case oleh Keisuke Yoshikawa, Motoi Kuwahara, Kazumasa Saigoh, Hiroyuki Ishiura, Yuko Yamagishi, Yuta Hamano, Makoto Samukawa, Hidekazu Suzuki, Makito Hirano, Yoshiyuki Mitsui, Shoji Tsuji, Susumu Kusunoki

    Diterbitkan 2019-03-01
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  8. 8
    Valosin-containing protein Asp395Gly mutation in a patient with frontotemporal dementia: a case report

    Valosin-containing protein Asp395Gly mutation in a patient with frontotemporal dementia: a case report oleh Ryota Kobayashi, Hiroya Naruse, Shinobu Kawakatsu, Chifumi Iseki, Yuya Suzuki, Shingo Koyama, Daichi Morioka, Hiroyuki Ishiura, Jun Mitsui, Yasuyuki Ohta, Shoji Tsuji, Tatsushi Toda, Koichi Otani

    Diterbitkan 2022-11-01
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  9. 9
    Identification of ATP1A3 mutations by exome sequencing as the cause of alternating hemiplegia of childhood in Japanese patients.

    Identification of ATP1A3 mutations by exome sequencing as the cause of alternating hemiplegia of childhood in Japanese patients. oleh Atsushi Ishii, Yoshiaki Saito, Jun Mitsui, Hiroyuki Ishiura, Jun Yoshimura, Hidee Arai, Sumimasa Yamashita, Sadami Kimura, Hirokazu Oguni, Shinichi Morishita, Shoji Tsuji, Masayuki Sasaki, Shinichi Hirose

    Diterbitkan 2013-01-01
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  10. 10
    SLC4A4 compound heterozygous mutations in exon–intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner’s syndrome: a case report

    SLC4A4 compound heterozygous mutations in exon–intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner’s syndr... oleh Shoko Horita, Enver Simsek, Tulay Simsek, Nilgun Yildirim, Hiroyuki Ishiura, Motonobu Nakamura, Nobuhiko Satoh, Atsushi Suzuki, Hiroyuki Tsukada, Tomohito Mizuno, George Seki, Shoji Tsuji, Masaomi Nangaku

    Diterbitkan 2018-06-01
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  11. 11
    Multi-type RFC1 repeat expansions as the most common cause of hereditary sensory and autonomic neuropathy

    Multi-type RFC1 repeat expansions as the most common cause of hereditary sensory and autonomic neuropathy oleh Jun-Hui Yuan, Yujiro Higuchi, Masahiro Ando, Eiji Matsuura, Akihiro Hashiguchi, Akiko Yoshimura, Tomonori Nakamura, Yusuke Sakiyama, Jun Mitsui, Hiroyuki Ishiura, Shoji Tsuji, Shoji Tsuji, Hiroshi Takashima

    Diterbitkan 2022-08-01
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  12. 12
    SNP haplotype mapping in a small ALS family.

    SNP haplotype mapping in a small ALS family. oleh Katherine A Dick Krueger, Shoji Tsuji, Yoko Fukuda, Yuji Takahashi, Jun Goto, Jun Mitsui, Hiroyuki Ishiura, Joline C Dalton, Michael B Miller, John W Day, Laura P W Ranum

    Diterbitkan 2009-05-01
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  13. 13
    Proteomic profile of nuclei containing p62-positive inclusions in a patient with neuronal intranuclear inclusion disease

    Proteomic profile of nuclei containing p62-positive inclusions in a patient with neuronal intranuclear inclusion disease oleh Masanori Kurihara, Tatsuo Mano, Fumihiro Eto, Ikuko Yao, Kenichiro Sato, Gaku Ohtomo, Taro Bannai, Shota Shibata, Hiroyuki Ishiura, Masako Ikemura, Tomoyasu Matsubara, Maho Morishima, Yuko Saito, Shigeo Murayama, Tatsushi Toda, Mitsutoshi Setou, Atsushi Iwata

    Diterbitkan 2023-02-01
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  14. 14
    Novel de novo POLR3B mutations responsible for demyelinating Charcot–Marie–Tooth disease in Japan

    Novel de novo POLR3B mutations responsible for demyelinating Charcot–Marie–Tooth disease in Japan oleh Masahiro Ando, Yujiro Higuchi, Jun‐Hui Yuan, Akiko Yoshimura, Ruriko Kitao, Takehiko Morimoto, Takaki Taniguchi, Mika Takeuchi, Jun Takei, Yu Hiramatsu, Yusuke Sakiyama, Akihiro Hashiguchi, Yuji Okamoto, Jun Mitsui, Hiroyuki Ishiura, Shoji Tsuji, Hiroshi Takashima

    Diterbitkan 2022-05-01
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  15. 15
    Comprehensive Genetic Analyses of Inherited Peripheral Neuropathies in Japan: Making Early Diagnosis Possible

    Comprehensive Genetic Analyses of Inherited Peripheral Neuropathies in Japan: Making Early Diagnosis Possible oleh Masahiro Ando, Yujiro Higuchi, Junhui Yuan, Akiko Yoshimura, Takaki Taniguchi, Fumikazu Kojima, Yutaka Noguchi, Takahiro Hobara, Mika Takeuchi, Jun Takei, Yu Hiramatsu, Yusuke Sakiyama, Akihiro Hashiguchi, Yuji Okamoto, Jun Mitsui, Hiroyuki Ishiura, Shoji Tsuji, Hiroshi Takashima

    Diterbitkan 2022-06-01
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  16. 16
    SPTLC2 variants are associated with early‐onset ALS and FTD due to aberrant sphingolipid synthesis

    SPTLC2 variants are associated with early‐onset ALS and FTD due to aberrant sphingolipid synthesis oleh Hiroya Naruse, Hiroyuki Ishiura, Kayoko Esaki, Jun Mitsui, Wataru Satake, Peter Greimel, Nanoka Shingai, Yuka Machino, Yasumasa Kokubo, Hirotoshi Hamaguchi, Tetsuya Oda, Tomoko Ikkaku, Ichiro Yokota, Yuji Takahashi, Yuta Suzuki, Takashi Matsukawa, Jun Goto, Kishin Koh, Yoshihisa Takiyama, Shinichi Morishita, Takeo Yoshikawa, Shoji Tsuji, Tatsushi Toda

    Diterbitkan 2024-04-01
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  17. 17
    A case of intravascular lymphoma presenting with a lesion in the splenium of the corpus callosum

    A case of intravascular lymphoma presenting with a lesion in the splenium of the corpus callosum oleh Haruka Masuzawa, MD, Fumio Suzuki, MD, PhD, Shiori Amemiya, MD, PhD, Kenta Orimo, MD, Hiroyuki Ishiura, MD, PhD, Ryo Hara, MD, Tatsushi Toda, MD, PhD, Teruo Nakazawa, MD, Akira Honda, MD, PhD, Mariko Tanaka, MD, PhD, Munetoshi Hinata, MD, PhD, Osamu Abe, MD, PhD

    Diterbitkan 2023-05-01
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  18. 18
    Ataxic phenotype with altered CaV3.1 channel property in a mouse model for spinocerebellar ataxia 42

    Ataxic phenotype with altered CaV3.1 channel property in a mouse model for spinocerebellar ataxia 42 oleh Shunta Hashiguchi, Hiroshi Doi, Misako Kunii, Yukihiro Nakamura, Misa Shimuta, Etsuko Suzuki, Shigeru Koyano, Masaki Okubo, Hitaru Kishida, Masaaki Shiina, Kazuhiro Ogata, Fumiko Hirashima, Yukichi Inoue, Shun Kubota, Noriko Hayashi, Haruko Nakamura, Keita Takahashi, Atsuko Katsumoto, Mikiko Tada, Kenichi Tanaka, Toshikuni Sasaoka, Satoko Miyatake, Noriko Miyake, Hirotomo Saitsu, Nozomu Sato, Kokoro Ozaki, Kiyobumi Ohta, Takanori Yokota, Hidehiro Mizusawa, Jun Mitsui, Hiroyuki Ishiura, Jun Yoshimura, Shinichi Morishita, Shoji Tsuji, Hideyuki Takeuchi, Kinya Ishikawa, Naomichi Matsumoto, Taro Ishikawa, Fumiaki Tanaka

    Diterbitkan 2019-10-01
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  19. 19
    Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2

    Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2 oleh Mark A. Corbett, Thessa Kroes, Liana Veneziano, Mark F. Bennett, Rahel Florian, Amy L. Schneider, Antonietta Coppola, Laura Licchetta, Silvana Franceschetti, Antonio Suppa, Aaron Wenger, Davide Mei, Manuela Pendziwiat, Sabine Kaya, Massimo Delledonne, Rachel Straussberg, Luciano Xumerle, Brigid Regan, Douglas Crompton, Anne-Fleur van Rootselaar, Anthony Correll, Rachael Catford, Francesca Bisulli, Shreyasee Chakraborty, Sara Baldassari, Paolo Tinuper, Kirston Barton, Shaun Carswell, Martin Smith, Alfredo Berardelli, Renee Carroll, Alison Gardner, Kathryn L. Friend, Ilan Blatt, Michele Iacomino, Carlo Di Bonaventura, Salvatore Striano, Julien Buratti, Boris Keren, Caroline Nava, Sylvie Forlani, Gabrielle Rudolf, Edouard Hirsch, Eric Leguern, Pierre Labauge, Simona Balestrini, Josemir W. Sander, Zaid Afawi, Ingo Helbig, Hiroyuki Ishiura, Shoji Tsuji, Sanjay M. Sisodiya, Giorgio Casari, Lynette G. Sadleir, Riaan van Coller, Marina A. J. Tijssen, Karl Martin Klein, Arn M. J. M. van den Maagdenberg, Federico Zara, Renzo Guerrini, Samuel F. Berkovic, Tommaso Pippucci, Laura Canafoglia, Melanie Bahlo, Pasquale Striano, Ingrid E. Scheffer, Francesco Brancati, Christel Depienne, Jozef Gecz

    Diterbitkan 2019-10-01
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  20. 20
    CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia

    CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia oleh Kelly L. Williams, Simon Topp, Shu Yang, Bradley Smith, Jennifer A. Fifita, Sadaf T. Warraich, Katharine Y. Zhang, Natalie Farrawell, Caroline Vance, Xun Hu, Alessandra Chesi, Claire S. Leblond, Albert Lee, Stephanie L. Rayner, Vinod Sundaramoorthy, Carol Dobson-Stone, Mark P. Molloy, Marka van Blitterswijk, Dennis W. Dickson, Ronald C. Petersen, Neill R. Graff-Radford, Bradley F. Boeve, Melissa E. Murray, Cyril Pottier, Emily Don, Claire Winnick, Emily P. McCann, Alison Hogan, Hussein Daoud, Annie Levert, Patrick A. Dion, Jun Mitsui, Hiroyuki Ishiura, Yuji Takahashi, Jun Goto, Jason Kost, Cinzia Gellera, Athina Soragia Gkazi, Jack Miller, Joanne Stockton, William S. Brooks, Karyn Boundy, Meraida Polak, José Luis Muñoz-Blanco, Jesús Esteban-Pérez, Alberto Rábano, Orla Hardiman, Karen E. Morrison, Nicola Ticozzi, Vincenzo Silani, Jacqueline de Belleroche, Jonathan D. Glass, John B. J. Kwok, Gilles J. Guillemin, Roger S. Chung, Shoji Tsuji, Robert H. Brown, Alberto García-Redondo, Rosa Rademakers, John E. Landers, Aaron D. Gitler, Guy A. Rouleau, Nicholas J. Cole, Justin J. Yerbury, Julie D. Atkin, Christopher E. Shaw, Garth A. Nicholson, Ian P. Blair

    Diterbitkan 2016-04-01
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