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J-GLOBAL ID:202001002469143782   Update date: Dec. 27, 2024

Yoshino Hiroyo

ヨシノ ヒロヨ | Yoshino Hiroyo
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Affiliation and department:
Research theme for competitive and other funds  (3):
  • 2022 - 2025 神経変性疾患関連遺伝子VPS13のパーキンソン病におけるリスク因子の解明
  • 2018 - 2021 Genetic analysis of VPS13C in Parkinson's disease
  • 2008 - 2010 Gene analysis of amyotrophic lateral sclerosis/parkinsonism-dementia complex, Kii, Japan
Papers (113):
  • Kensuke Daida, Hiroyo Yoshino, Laksh Malik, Breeana Baker, Mayu Ishiguro, Rylee Genner, Kimberly Paquette, Yuanzhe Li, Kenya Nishioka, Satoshi Masuzugawa, et al. The Utility of Long-Read Sequencing in Diagnosing Early Onset Parkinson's Disease. Annals of neurology. 2024
  • Mayuko Imura, Keiichi Nakahara, Kentaro Hara, Hiroyo Yoshino, Kenya Nishioka, Nobutaka Hattori, Mitsuharu Ueda. Rapidly Progressive Gait Disturbance and Extensive Iron Deposits in Late-Onset MPAN With a Pathogenic C19orf12 Variant: An 8-Year Follow-up. Neurology. 2024. 103. 4. e209724
  • Aya Ikeda, Hongrui Meng, Daisuke Taniguchi, Muneyo Mio, Manabu Funayama, Kenya Nishioka, Mari Yoshida, Yuanzhe Li, Hiroyo Yoshino, Tsuyoshi Inoshita, et al. CHCHD2 P14L, found in amyotrophic lateral sclerosis, exhibits cytoplasmic mislocalization and alters Ca2+ homeostasis. PNAS Nexus. 2024. 3. 8
  • Mayuko Imura, Keiichi Nakahara, Kentaro Hara, Hiroyo Yoshino, Kenya Nishioka, Nobutaka Hattori, Mitsuharu Ueda. Rapidly Progressive Gait Disturbance and Extensive Iron Deposits in Late-Onset MPAN With a Pathogenic C19orf12 Variant An 8-Year Follow-up. Neurology. 2024. 103. 4
  • 中原 圭一, 井村 麻由子, 原 健太朗, 吉野 浩代, 西岡 健弥, 服部 信孝, 植田 光晴. C19orf12遺伝子のホモ接合型新規変異を伴う晩発性MPANの病態解析. パーキンソン病・運動障害疾患コングレスプログラム・抄録集. 2024. 18回. 105-105
more...
MISC (68):
  • Yamashita Yuri, Tagai Kenji, Shimada Hitoshi, Shimonaka Shotaro, Yoshino Hiroyo, Li Yuanzhe, Oyama Genko, Saiki Shinji, Hatano Taku, Matsuoka Kiwamu, et al. MAPT p.K298_H299insQ患者におけるタウ凝集の性質と臨床的特徴との関連性(Property of tau aggregation and its relation with clinical features in MAPT p.K298_H299insQ patients). 臨床神経学. 2021. 61. Suppl. S357-S357
  • 西岡健弥, 山下由莉, 互健二, 島田斉, 吉野浩代, 李元哲, 舩山学, 舩山学, 樋口真, 服部信孝, et al. 新規変異MAPT p.K298_H299insQのタウイメージングと臨床遺伝学的解析. 日本人類遺伝学会大会プログラム・抄録集. 2021. 66th
  • 吉野 浩代, 服部 信孝. 【パーキンソン病(第2版)-基礎・臨床研究のアップデート-】 病因 原因・関連遺伝子 GCH1遺伝子. 日本臨床. 2018. 76. 増刊4 パーキンソン病. 135-139
  • Nakayama Sachiko, Shimonaka Shotaro, Elahi Montasir, Oji Yutaka, Li Yuanzhe, Hiroyo Yoshino, Nishioka Kenya, Hatano Taku, Motoi Yumiko, Hattori Nobutaka. 新規MAPT遺伝子変異 臨床的および生化学的解析(New Mutations in the MAPT Gene: Clinical and Biochemical Characterization). 順天堂醫事雑誌. 2017. 63. 6. 489-490
  • 服部 達哉, 服部 優子, 後藤 洋二, 吉野 浩代, 服部 信孝. ドーパミントランスポーターSPECT(DAT SPECT)で高度集積低下のみられたbata-propeller protein-associated neurodegeneration(BPAN)の1例. 臨床神経学. 2017. 57. 12. 791-791
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Professional career (1):
  • 医学博士 (順天堂大学大学院医学研究科)
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