Rchr
J-GLOBAL ID:201801006904844086   Update date: Jan. 29, 2021

Kurosawa Kenji

Kurosawa Kenji
Research field  (1): Fetal medicine/Pediatrics
Papers (225):
  • Satomi Mori, Koji Tanoue, Hiroyuki Shimizu, Hiroyuki Nagafuchi, Ki-Sung Kim, Hiroaki Murakami, Kenji Kurosawa, Kiyoshi Matsui. Lung disease due to FLNA mutation improved after shunt closure for congenital heart disease. Pediatric pulmonology. 2021
  • Masayuki Sasaki, Noriko Sumitomo, Yuko Shimizu-Motohashi, Eri Takeshita, Kenji Kurosawa, Kenjiro Kosaki, Kazuhiro Iwama, Takeshi Mizuguchi, Naomichi Matsumoto. ATP1A3 variants and slowly progressive cerebellar ataxia without paroxysmal or episodic symptoms in children. Developmental medicine and child neurology. 2021. 63. 1. 111-115
  • Takayuki Yokoi, Yumi Enomoto, Yoshinori Tsurusaki, Kenji Kurosawa. Siblings with vascular Ehlers-Danlos syndrome inherited via maternal mosaicism. Congenital anomalies. 2020
  • Hitoshi Kashiki, Heng Li, Sachiko Miyamoto, Hiroe Ueno, Yoshinori Tsurusaki, Chizuru Ikeda, Hirofumi Kurata, Takumi Okada, Tomoyuki Shimazu, Hoseki Imamura, et al. POLR1C variants dysregulate splicing and cause hypomyelinating leukodystrophy. Neurology. Genetics. 2020. 6. 6. e524
  • Mio Tsuchiya, Takahiro Yamada, Rina Akaishi, Haruka Hamanoue, Akira Hirasawa, Maki Hyodo, Issei Imoto, Tomoki Kosho, Kenji Kurosawa, Hiromi Murakami, et al. Attitudes toward and current status of disclosure of secondary findings from next-generation sequencing: a nation-wide survey of clinical genetics professionals in Japan. Journal of human genetics. 2020. 65. 12. 1045-1053
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MISC (516):
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Books (1):
  • 新先天奇形症候群アトラス
    南江堂 2015 ISBN:9784524242887
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