Nonalcoholic fatty liver disease with prolactin-secreting pituitary adenoma in an adolescent: A case report

by Takaki, Yugo, Mizuochi, Tatsuki, Nishioka, Junko, Eda, Keisuke, Yatsuga, Shuichi, Yamashita, Yushiro
Published in Medicine (Baltimore) (2018)

SAT-426 Macro-Thyroid Stimulating Hormone (TSH) in Children

by Hattori, Naoki, Matsuda, Takeshi, Chihara, Kazuhisa, Nishioka, Junko, Elmaoğulları, Selin, Shimatsu, Akira
Published in J Endocr Soc (2020)

A two-day-old hyperthyroid neonate with thyroid hormone resistance born to a mother with well-controlled Graves’ disease: a case report

by Yatsuga, Shuichi, Hiromatsu, Yuji, Sasaki, Shigekazu, Nakamura, Hirotoshi, Katayama, Koju, Nishioka, Junko, Koga, Yasutoshi
Published 2012

Developmental delay and failure to thrive in a 7-month-old baby boy with spontaneous transient Graves’ thyrotoxicosis: a case report

by Yatsuga, Shuichi, Saikusa, Tomoko, Sasaki, Takako, Ushijima, Kikumi, Kitamura, Miyuki, Nishioka, Junko, Koga, Yasutoshi
Published in J Med Case Rep (2016)

The first Japanese case of central precocious puberty with a novel MKRN3 mutation

by Nishioka, Junko, Shima, Hirohito, Fukami, Maki, Yatsuga, Shuichi, Matsumoto, Takako, Ushijima, Kikumi, Kitamura, Miyuki, Koga, Yasutoshi
Published in Hum Genome Var (2017)

Molecular and clinical analyses of two patients with UPD(16)mat detected by screening 94 patients with Silver-Russell syndrome phenotype of unknown aetiology

by Inoue, Takanobu, Yagasaki, Hideaki, Nishioka, Junko, Nakamura, Akie, Matsubara, Keiko, Narumi, Satoshi, Nakabayashi, Kazuhiko, Yamazawa, Kazuki, Fuke, Tomoko, Oka, Akira, Ogata, Tsutomu, Fukami, Maki, Kagami, Masayo
Published in J Med Genet (2019)

(Epi)genetic defects of MKRN3 are rare in Asian patients with central precocious puberty

by Suzuki, Erina, Shima, Hirohito, Kagami, Masayo, Soneda, Shun, Tanaka, Toshiaki, Yatsuga, Shuichi, Nishioka, Junko, Oto, Yuji, Kamiya, Toshiya, Naiki, Yasuhiro, Ogata, Tsutomu, Fujisawa, Yasuko, Nakamura, Akie, Kawashima, Sayaka, Morikawa, Shuntaro, Horikawa, Reiko, Sano, Shinichiro, Fukami, Maki
Published in Hum Genome Var (2019)

Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients

by Inoue, Takanobu, Nakamura, Akie, Iwahashi-Odano, Megumi, Tanase-Nakao, Kanako, Matsubara, Keiko, Nishioka, Junko, Maruo, Yoshihiro, Hasegawa, Yukihiro, Suzumura, Hiroshi, Sato, Seiji, Kobayashi, Yoshiyuki, Murakami, Nobuyuki, Nakabayashi, Kazuhiko, Yamazawa, Kazuki, Fuke, Tomoko, Narumi, Satoshi, Oka, Akira, Ogata, Tsutomu, Fukami, Maki, Kagami, Masayo
Published in Clin Epigenetics (2020)