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Kaori Fujikura
Kaori Fujikura
Internal medicine
Endocrinology
Biology
Mutation
Gene
5
Papers
39
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Association of maternal serum concentration of hydroxylated polychlorinated biphenyls with maternal and neonatal thyroid hormones: The Hokkaido birth cohort study
2018
Environmental Research
Sachiko Itoh
Toshiaki Baba
Motoyuki Yuasa
Chihiro Miyashita
Sumitaka Kobayashi
Atsuko Araki
Seiko Sasaki
Jumboku Kajiwara
Tsuguhide Hori
Takashi Todaka
Kaori Fujikura
Sonomi Nakajima
Shizue Kato
Reiko Kishi
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Citations (15)
Novel CYP17A1 mutation in a Japanese patient with combined 17α-hydroxylase/17,20-lyase deficiency
2010
Metabolism-clinical and Experimental
Noriyuki Katsumata
Eishin Ogawa
Ikuma Fujiwara
Kaori Fujikura
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Novel intronic CYP21A2 mutation in a Japanese patient with classic salt-wasting steroid 21-hydroxylase deficiency
2010
Metabolism-clinical and Experimental
Noriyuki Katsumata
Takashi Shinagawa
Reiko Horikawa
Kaori Fujikura
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Citations (6)
IVS9-9C>A, not IVS9-9A>C, mutation in CYP21A2 causes classic salt-wasting steroid 21-hydroxylase deficiency
2010
Metabolism-clinical and Experimental
Noriyuki Katsumata
Takashi Shinagawa
Reiko Horikawa
Kaori Fujikura
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A study on "open to blow" of housing with CAD : The psychological effects of humans in a space
2000
Megumi Yanai
Haruki Yasuhara
Yasuo Inoue
Shizuki Okamoto
Motoki Koh
Tatuya Iwabu
Yasumasa Otoguro
Eiko Sakai
Keiko Takano
Kaori Fujikura
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