Rchr
J-GLOBAL ID:201901005063670380   Update date: Feb. 15, 2024

Miura Shiroh

Miura Shiroh
Affiliation and department:
Research field  (1): Neurology
Research keywords  (1): 遺伝性神経疾患
Research theme for competitive and other funds  (1):
  • 2014 - 2017 Genetic analysis of novel hereditary neuropathy mapping to chromosome 1
Papers (77):
  • Shiroh Miura, Emina Watanabe, Kensuke Senzaki, Shigeyoshi Hiruki, Sayaka Matsumoto, Takuya Morikawa, Yusuke Uchiyama, Seiji Kurata, Masayuki Ochi, Yasumasa Ohyagi, et al. Episodic ataxia type 2 with a novel missense variant (Leu602Arg) in CACNA1A. Human Genome Variation. 2024
  • 岡部 颯, 松本 清香, 藤下 幸穂, 武井 聡子, 岡田 陽子, 越智 雅之, 三浦 史郎, 越智 博文, 伊賀瀬 道也, 大八木 保政. 長大な脊髄炎様病変と免疫介在性血小板減少症を呈した脊髄髄内原発悪性リンパ腫の1例. 臨床神経学. 2023. 63. 9. 620-620
  • Seiko Koizumi, Yoko Okada, Shiroh Miura, Yuuki Imai, Keiji Igase, Yasumasa Ohyagi, Michiya Igase. Ingestion of a collagen peptide containing high concentrations of prolyl-hydroxyproline and hydroxyprolyl-glycine reduces advanced glycation end products levels in the skin and subcutaneous blood vessel walls: a randomized, double-blind, placebo-controlled study. Bioscience, biotechnology, and biochemistry. 2023
  • 武井 聡子, 千崎 健佑, 越智 雅之, 藤下 幸穂, 松本 清香, 岡田 陽子, 三浦 史郎, 越智 博文, 伊賀瀬 道也, 大八木 保政. Valosin-containing protein(VCP)遺伝子ミスセンス変異を伴うALS+FTDの1例. 臨床神経学. 2023. 63. 5. 319-319
  • Takuya Morikawa, Masatomo Takahashi, Yoshihiro Izumi, Takeshi Bamba, Kosei Moriyama, Gohsuke Hattori, Ryuta Fujioka, Shiroh Miura, Hiroki Shibata. Oleic Acid-Containing Phosphatidylinositol Is a Blood Biomarker Candidate for SPG28. Biomedicines. 2023
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MISC (78):
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Education (2):
  • 九州大学大学院 医学系研究科
  • Kyushu University School of Medicine
Work history (4):
  • Duke University Medical Center Center for Human Genetics
  • 久留米大学病院
  • 松山赤十字病院
  • 九州大学医学部附属病院
Association Membership(s) (2):
日本人類遺伝学会 ,  日本内科学会
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