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OGASAWARA MASASHI  小笠原 真志

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小笠原 真志  オガサワラ マサシ

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Researcher Number 70827617
Other IDs
Affiliation (Current) 2025: 国立研究開発法人国立精神・神経医療研究センター, 神経研究所 疾病研究第一部, 研究生
Affiliation (based on the past Project Information) *help 2023: 国立研究開発法人国立精神・神経医療研究センター, 神経研究所 疾病研究第一部, 研究生
2020: 国立研究開発法人国立精神・神経医療研究センター, メディカルゲノムセンター, リサーチフェロー
Review Section/Research Field
Principal Investigator
Basic Section 52020:Neurology-related
Keywords
Principal Investigator
先天性ミオパチー / 筋力低下 / NEB / ネマリンミオパチー / カルシウム / Tubular aggregates / Congenital myopathy / STIM1 / ORAI1 / ATP1A2 / Tubular aggregate
  • Research Projects

    (2 results)
  • Research Products

    (9 results)
  • Co-Researchers

    (1 People)
  •  NEB関連ミオパチーにおける臨床病理学的な遺伝子型・表現型相関とその自然歴の解明Principal Investigator

    • Principal Investigator
      小笠原 真志
    • Project Period (FY)
      2023 – 2025
    • Research Category
      Grant-in-Aid for Early-Career Scientists
    • Review Section
      Basic Section 52020:Neurology-related
    • Research Institution
      National Center of Neurology and Psychiatry
  •  ATP1A2遺伝子変異は管状凝集体ミオパチーを引き起こすか?Principal Investigator

    • Principal Investigator
      小笠原 真志
    • Project Period (FY)
      2020
    • Research Category
      Grant-in-Aid for Early-Career Scientists
    • Review Section
      Basic Section 52020:Neurology-related
    • Research Institution
      National Center of Neurology and Psychiatry

All 2023 2020

All Journal Article Presentation

  • [Journal Article] 特集 小児科医が知っておくべき筋疾患診療:遺伝学的理解と治療の最新事情 代表的筋疾患 先天性ミオパチー2023

    • Author(s)
      小笠原 真志
    • Journal Title

      小児内科

      Volume: 55 Issue: 12 Pages: 1941-1945

    • DOI

      10.24479/pm.0000001432

    • ISSN
      0385-6305
    • Year and Date
      2023-12-01
    • Data Source
      KAKENHI-PROJECT-23K14766
  • [Journal Article] Coexistence of congenital central hypoventilation syndrome, Hirschsprung disease, and Becker muscular dystrophy2023

    • Author(s)
      Kawashima Yuki、Akiyama Satoka、Yamada Yosuke、Noda Masahiro、Oba Kunihiro、Komaki Hirofumi、Komori Koji、Sasaki Ayako、Ogasawara Masashi
    • Journal Title

      Brain and Development Case Reports

      Volume: 1 Issue: 1 Pages: 100003-100003

    • DOI

      10.1016/j.bdcasr.2023.100003

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-23K14766
  • [Journal Article] Evaluation of the Core Formation Process in Congenital Neuromuscular Disease With Uniform Type 1 Fiber and Central Core Disease2020

    • Author(s)
      Ogasawara Masashi、Ogawa Megumu、Nonaka Ikuya、Hayashi Shinichiro、Noguchi Satoru、Nishino Ichizo
    • Journal Title

      Journal of Neuropathology & Experimental Neurology

      Volume: 79 Issue: 12 Pages: 1370-1375

    • DOI

      10.1093/jnen/nlaa104

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18K07082, KAKENHI-PROJECT-20K16612
  • [Presentation] Coexistence of Congenital Central Hypoventilation Syndrome and Becker Muscular Dystrophy2023

    • Author(s)
      Yuki Kawashima, Satoka Akiyama, Yosuke Yamada, Masahiro Noda, Kunihiro Oba, Hirofumi Komaki, Koji Komori, Ayako Sasaki, Masashi Ogasawara.
    • Organizer
      16th Asian-Oceanian Congress of Child Neurology (AOCCN 2023)
    • Data Source
      KAKENHI-PROJECT-23K14766
  • [Presentation] Deep convolutional-neural-network can differentiate twelve major muscular diseases better than human2020

    • Author(s)
      Kabeya Y, Okubo M, Yonezawa S, Nakano H, Inoue M, Ogasawara M, Saito Y, Tanboon J, Indrawati L, Kumutpongpanich T, Chen Y, Tokumasu R, Iwamori T, Takano A, Nishino I
    • Organizer
      25th International Congress of the World Muscle Society (国際学会)
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20K16612
  • [Presentation] イントロン変異を原因とする筋ジストロフィーの治療2020

    • Author(s)
      大原寛明,細川元靖,粟屋智就,髙橋良輔,小笠原真志,野口 悟,後藤雄一,西野一三,萩原正敏
    • Organizer
      第6回日本筋学会学術集会
    • Data Source
      KAKENHI-PROJECT-20K16612
  • [Presentation] Congenital neuromuscular disease with uniform type 1 fiber due to RYR1 mutation is a de facto core myopathy2020

    • Author(s)
      Ogasawara M, Ogawa M, Nonaka I, Hayashi S, Noguchi S, Nishino I
    • Organizer
      25th International Congress of the World Muscle Society (国際学会)
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20K16612
  • [Presentation] Pathogenesis of congenital neuromuscular disease with uniform type 1 fiber and central core disease.2020

    • Author(s)
      Ogasawara M, Ogawa M, Hayashi S, Nonaka I, Noguchi S, Nishino I
    • Organizer
      第62回日本小児神経学会学術集会
    • Data Source
      KAKENHI-PROJECT-20K16612
  • [Presentation] Myopathy in scleroderma/systemic sclerosis patients: From a histopathological point of view.2020

    • Author(s)
      Chen Y, Inoue M, Ogasawara M, Saito Y, Indrawati L, Tanboon J, Kumutpongpanich T, Okubo M, Yoshioka W, Hayashi S, Noguchi S, Nishino I
    • Organizer
      25th International Congress of the World Muscle Society (国際学会)
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20K16612
  • 1.  林 晋一郎
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results

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