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

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

OGASAWARA MASASHI 小笠原 真志

小笠原 真志 オガサワラ マサシ

Research Projects

Research Products

Co-Researchers

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

Project Period (FY)

Research Category

Review Section

Research Institution

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

Project Period (FY)

Research Category

Review Section

Research Institution

[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)

Journal Title

DOI

ISSN

Year and Date

Data Source

[Journal Article] Coexistence of congenital central hypoventilation syndrome, Hirschsprung disease, and Becker muscular dystrophy2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Evaluation of the Core Formation Process in Congenital Neuromuscular Disease With Uniform Type 1 Fiber and Central Core Disease2020

Author(s)

Journal Title

DOI

Data Source

[Presentation] Coexistence of Congenital Central Hypoventilation Syndrome and Becker Muscular Dystrophy2023

Author(s)

Organizer

Data Source

[Presentation] Deep convolutional-neural-network can differentiate twelve major muscular diseases better than human2020

Author(s)

Organizer

Data Source

[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)

Organizer

Data Source

[Presentation] Congenital neuromuscular disease with uniform type 1 fiber due to RYR1 mutation is a de facto core myopathy2020

Author(s)

Organizer

Data Source

[Presentation] Pathogenesis of congenital neuromuscular disease with uniform type 1 fiber and central core disease.2020

Author(s)

Organizer

Data Source

[Presentation] Myopathy in scleroderma/systemic sclerosis patients: From a histopathological point of view.2020

Author(s)

Organizer

Data Source

OGASAWARA MASASHI 小笠原真志

小笠原真志オガサワラマサシ

[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