Rchr
J-GLOBAL ID:201901001077673859   Update date: Mar. 23, 2024

Eura Nobuyuki

エウラ ノブユキ | Eura Nobuyuki
Affiliation and department:
Research field  (4): Medical biochemistry ,  Neuroanatomy and physiology ,  Neuroscience - general ,  Neurology
Research keywords  (5): Clinical genetics ,  Myology ,  induced pluripotent stem cells ,  Muscle Pathology ,  Neurology
Research theme for competitive and other funds  (4):
  • 2020 - 2023 Investigation of pathology of intractable central nervous disorders using human brain organoids
  • 2019 - 2020 ヒト脳オルガノイドを用いたMowat-Wilson症候群における中枢神経病変の病態解析
  • 2018 - 2019 オートファジー異常を呈する炎症性筋疾患の臨床病理学的検討
  • 2017 - 2018 オートファジー異常によるミオパチーの病態解明
Papers (118):
  • Shogo Komaki, Akatsuki Kubota, Kazuto Katsuse, Asuka Kitamura, Meiko Maeda, Takashi Matsukawa, Nobuyuki Eura, Yoshihiko Saito, Ichizo Nishino, Tatsushi Toda. A Case of a Patient with Calpainopathy Carrying Compound Heterozygous Mutations of a <i>de novo</i> Pathogenic Variant of c.1333G>A and a Novel Variant of c.1331C>T in <i>CAPN3</i>. Internal Medicine. 2024
  • Nobuyuki Eura, Satoru Noguchi, Masashi Ogasawara, Theerawat Kumutpongpanich, Shinichiro Hayashi, Ichizo Nishino. Characteristics of the muscle involvement along the disease progression in a large cohort of oculopharyngodistal myopathy compared to oculopharyngeal muscular dystrophy. Journal of neurology. 2023
  • Yoshiaki Takahashi, Nobutoshi Morimoto, Tomoaki Nada, Mizuki Morimoto, Nobuyuki Eura, Narihiro Minami, Ichizo Nishino. A Case of Oculopharyngeal Muscular Dystrophy Caused by a Novel PABPN1 c.34G > T (p.Gly12Trp) Point Mutation without Polyalanine Expansion. JOURNAL OF NEUROMUSCULAR DISEASES. 2023. 10. 3. 459-463
  • Yoshiaki Takahashi, Nobutoshi Morimoto, Tomoaki Nada, Mizuki Morimoto, Nobuyuki Eura, Narihiro Minami, Ichizo Nishino. A Case of Oculopharyngeal Muscular Dystrophy Caused by a Novel PABPN1 c.34G > T (p.Gly12Trp) Point Mutation without Polyalanine Expansion. Journal of neuromuscular diseases. 2023. 10. 3. 459-463
  • Nobuyuki Eura, Aritoshi Iida, Masashi Ogasawara, Shinichiro Hayashi, Satoru Noguchi, Ichizo Nishino. RILPL1-related OPDM is absent in a Japanese cohort. American journal of human genetics. 2022. 109. 11. 2088-2089
more...
MISC (12):
more...
Lectures and oral presentations  (30):
  • 核内封入体によって眼咽頭型筋ジストロフィーと眼咽頭遠位型ミオパチーは鑑別しうる
    (第7回日本筋学会学術大会)
  • Exploring the mechanism of myogenic and neurogenic changes on electromyography by quantifying muscle pathology in sporadic inclusion body myositis
    (The 26th Annual Congress of the World Muscle Society)
  • A 48-year-old man with progressive facial, bulbar and distal predominant limb weakness
    (The 20th Annual Scientific Meeting of Asian Oceanian Myology Center 2021)
  • Comparison of electromyography and quantified muscle pathology in sporadic inclusion body myositis
    (The 62nd Annual Meeting of the Japanese Society of Neurology)
  • ヒト多能性幹細胞を用いた脳幹オルガノイドの開発
    (第14回パーキンソン病・運動障害疾患コングレス 2021)
more...
Education (1):
  • 2002 - 2008 Nara Medical University Medical Faculty Medical Department
Professional career (1):
  • M.D., Ph.D. (Nara Medical University)
Work history (8):
  • 2023/04 - 現在 Nara Medical University Neurology
  • 2021/04 - 2023/03 National Center of Neurology and Psychiatry Department of Neuromuscular Research
  • 2018/07 - 2021/03 Nara Medical University Neurology Assistant Professor
  • 2013/11 - 2018/06 Nara Medical University
  • 2013/04 - 2013/10 Nara Medical University
Show all
Awards (1):
  • 2020/12 - 奈良県医師会 2020年度 奈良県医師会学術奨励賞
Association Membership(s) (12):
THE JAPANESE SOCIETY OF NEUROPATHOLOGY ,  日本頭痛学会 ,  JAPAN SOCIETY FOR HIGHER BRAIN DYSFUNCTION ,  THE JAPANESE ASSOCIATION OF REHABILITATION MEDICINE ,  JAPANESE PERIPHERAL NERVE SOCIETY ,  World Muscle Society ,  THE JAPAN STROKE SOCIETY ,  THE JAPANESE SOCIETY OF INTERNAL MEDICINE ,  THE JAPAN SOCIETY OF HUMAN GENETICS ,  日本筋学会 ,  日本神経治療学会 ,  JAPANESE SOCIETY OF NEUROLOGY
※ Researcher’s information displayed in J-GLOBAL is based on the information registered in researchmap. For details, see here.

Return to Previous Page