Rchr
J-GLOBAL ID：202401000593517620   Update date: Feb. 11, 2025

Hara Munetsugu

ハラ ムネツグ | Hara Munetsugu
Affiliation and department：
Kurume University Department of Pediatrics and Child Health

About Kurume University Department of Pediatrics and Child Health


Job title： Assistant Professor
Research field  (3)： Nervous system function ,  Neuroscience - general ,  Fetal medicine/Pediatrics
Research keywords  (5)： Pediatrics ,  Genetic Medicine ,  Rett syndrome ,  Autism Spectrum Disorder ,  Pediatric Neurology
Research theme for competitive and other funds  (4)：
  • 2024 - Clinical Research on Rett Syndrome and Related Disorders
  • 2021 - 2024 Does neurotransmitter switch of autonomic nerve lead to disturb heart-brain interaction of Rett syndrome?
  • 2014 - 2016 The study of impaired autonomic nerve system in Rett syndrome model mice and ES/iPS cells derived from them
  • 2012 - 2014 Development of a new therapy for Rett syndrome model iPS cells and mouse by recombinant Ghrelin
Papers (20)：
  • Munetsugu Hara, Toyojiro Matsuishi, Satoru Takahashi, Yushiro Yamashita. Sertraline treatment for paroxysmal nonkinesigenic dyskinesia comorbid with anxiety and depression. eNeurologicalSci. 2024. 36. 100520-100520
  • Syun Yoshida, Masano Amamoto, Tomoyuki Takahashi, Ichiro Tomita, Kotaro Yuge, Munetsugu Hara, Kazuhiro Iwama, Naomichi Matsumoto, Toyojiro Matsuishi. Perampanel markedly improved clinical seizures in a patient with a Rett-like phenotype and 960-kb deletion on chromosome 9q34.11 including the STXBP1. Clinical case reports. 2022. 10. 5. e05811
  • Atsushi Takata, Mitsuko Nakashima, Hirotomo Saitsu, Takeshi Mizuguchi, Satomi Mitsuhashi, Yukitoshi Takahashi, Nobuhiko Okamoto, Hitoshi Osaka, Kazuyuki Nakamura, Jun Tohyama, et al. Comprehensive analysis of coding variants highlights genetic complexity in developmental and epileptic encephalopathy. Nature Communications. 2019. 10. 1. 2506-2506
  • Tomoko Saikusa, Munetsugu Hara, Kazuhiro Iwama, Kotaro Yuge, Chihiro Ohba, Jun ichiro Okada, Tadashi Hisano, Yushiro Yamashita, Nobuhiko Okamoto, Hirotomo Saitsu, et al. De novo HDAC8 mutation causes Rett-related disorder with distinctive facial features and multiple congenital anomalies. Brain and Development. 2018. 40. 5. 406-409
  • Hiroshi Kida, Tomoyuki Takahashi, Yuki Nakamura, Takashi Kinoshita, Munetsugu Hara, Masaki Okamoto, Satoko Okayama, Keiichiro Nakamura, Ken Ichiro Kosai, Takayuki Taniwaki, et al. Pathogenesis of Lethal Aspiration Pneumonia in Mecp2-null Mouse Model for Rett Syndrome. Scientific Reports. 2017. 7. 1. 12032-12032
ｍore...
MISC (116)：
  • 金堂 円太郎, 阪田 健祐, 石井 隆大, 弓削 康太郎, 小池 敬義, 原 宗嗣, 水落 建輝, 古田 啓一郎, 森岡 基浩. インフルエンザA感染による意識障害と左上下肢の脱力を契機にもやもや病と診断した1例. 日本小児科学会雑誌. 2024. 128. 10. 1365-1365
  • 太田 光紀, 山下 大輔, 弓削 康太郎, 石井 隆大, 小池 敬義, 原 宗嗣, 山下 裕史朗. chorea,体幹失調により歩容異常を認めた2歳2ヵ月の女児例. 脳と発達. 2024. 56. 3. 225-225
  • 田中 裕大, 河野 剛, 泉 清徳, 弓削 康太郎, 原 宗嗣, 山下 裕史朗, 江島 伸興, 久村 悠祐, 松石 豊次郎. 視線解析装置を用いたRett症候群患者の視覚機能評価に関する検討. 脳と発達. 2024. 56. Suppl. S247-S247
  • 山下 大輔, 原 宗嗣, 石井 隆太, 弓削 康太郎, 小池 敬義, 藤野 武彦, 山下 裕史朗. 副腎白質ジストロフィー患児の病状変化とプラズマローゲンの推移に関する検討. 脳と発達. 2024. 56. Suppl. S266-S266
  • 後藤 康平, 八戸 由佳子, 弓削 康太郎, 山下 大輔, 石井 隆大, 小池 敬義, 木下 正啓, 原 宗嗣, 山下 裕史朗. 当院の現状から考えるトランジションの課題. 脳と発達. 2024. 56. Suppl. S288-S288
ｍore...
Patents (1)：
Books (5)：
  • 日常生活から学ぶ子どもの発達障害と睡眠
    診断と治療社 2024 ISBN:9784787826176
  • レット症候群診療ガイドブック
    大阪大学出版会 2015 ISBN:9784872594966
  • 厚生労働科学研究費補助金障害者対策総合研究事業(神経・筋疾患分野)レット症候群の早期診断と治療をめざした統合的研究研究報告書
    [国立精神・神経医療研究センター] 2013
  • 厚生労働科学研究費補助金難治性疾患克服研究事業レット症候群の診断と予防・治療法確立のための臨床および生物科学の集学的研究研究報告書
    [国立精神・神経医療研究センター神経研究所疾病研究第2部] 2011
  • 厚生労働科学研究費補助金難治性疾患克服研究事業レット症候群の診断と予防・治療法確立のための臨床および生物科学の集学的研究
    [国立精神・神経センター神経研究所疾病研究第2部] 2010
Education (1)：
  • 2008 - 2012 Kurume University Graduate School of Medicine Cognitive and Molecular Research Institute of Brain Diseases
Work history (2)：
  • 2017/08 - 2020/07 Vanderbilt University Medical Center Developmental Neuroscience, Department of Pediatrics Postdoctoral Researcher
  • 2016/10 - 2017/07 Department of Neuroscience, University of California San Diego Developmental Neuroscience, Postdoctoral Researcher
Awards (4)：
  • 2015/11 - the Pediatric subcommittee of the Kyushu society of medical science The 2015 Best Article Award at the Pediatric subcommittee of the Kyushu society of medical science Disturbance of cardiac gene expression and cardiomyocyte structure predisposes Mecp2-null mice to arrhythmias.
  • 2014/03 - Rett Syndrome Support Organization in Japan First Rett syndrome Research Award in Japan Elucidation of the Mechanisms of Arrhythmogenesis Using Rett Syndrome Model Animals and ES/iPS Cells
  • 2013/10 - Morinaga Volunteer Association 2013 Morinaga Volunteer Association Research Grant Exploratory Research on Pathological Predictive Markers of Growth and Developmental Disorders in Rett Syndrome
  • 2012/04 - Kurume University Academic Research Promotion Fund 2012 Kurume University Academic Research Promotion Fund Grant 「Development of Novel Therapies Using Ghrelin in the iPS Cells and Animals of Rett syndrome
Association Membership(s) (5)：
The Japan Society of Pediatric Genetics ,  The Asian and Oceanian Child Neurology Association ,  Japan Society of Human Genetics ,  The Japanese Society of Child Neurology ,  JAPAN PEDIATRIC SOCIETY
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