Disruption of the circadian rhythms and its relationship with pediatric obesity von Kawai, Masanobu

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Evaluations for Wilms tumor and late‐onset nephrotic syndrome in 46,XY DSD von Koizumi, Mikiko, Ida, Shinobu, Etani, Yuri, Kawai, Masanobu

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Renal function in short‐statured children born small for gestational age and treated with growth hormone von Koizumi, Mikiko, Ida, Shinobu, Shoji, Yasuko, Etani, Yuri, Kawai, Masanobu

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Ultrasonography for inguinal hernia led to the diagnosis of complete androgen insensitivity syndrome von Kubo, Hiroyuki, Kozan, Hiroko, Kawai, Masanobu

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Male assignment in 5α‐reductase type 2 deficiency with female external genitalia von Konishi, Ayako, Ida, Shinobu, Matsui, Futoshi, Etani, Yuri, Kawai, Masanobu

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Phosphate as a Signaling Molecule and Its Sensing Mechanism von Michigami, Toshimi, Kawai, Masanobu, Yamazaki, Miwa, Ozono, Keiichi

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Diagnostic Pitfall: Mosaic Turner syndrome with a 46, XY lymphocyte karyotype von Shoji, Yasuko, Ida, Shinobu, Kubo, Toshihide, Etani, Yuri, Kawai, Masanobu

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Skeletal Characteristics of Children and Adolescents with Turner Syndrome von Kawai, Masanobu, Hasegawa, Yukihiro

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Growth hormone treatment for extremely low birthweight children born small for gestational age von Onuma, Shinsuke, Ida, Shinobu, Maeyama, Takatoshi, Shoji, Yasuko, Etani, Yuri, Kawai, Masanobu

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Reductions in estimated glomerular filtration rate during puberty in GH-treated children born small for gestational age are associated with prematurity and low birth weight, not th... von Koizumi, Mikiko, Ida, Shinobu, Etani, Yuri, Kawai, Masanobu

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Lack of PTEN in osteocytes increases circulating phosphate concentrations by decreasing intact fibroblast growth factor 23 levels von Kawai, Masanobu, Kinoshita, Saori, Ozono, Keiichi, Michigami, Toshimi

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The Lack of Bmal1, a Core Clock Gene, in the Intestine Decreases Glucose Absorption in Mice von Onuma, Shinsuke, Kinoshita, Saori, Shimba, Shigeki, Ozono, Keiichi, Michigami, Toshimi, Kawai, Masanobu

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Factors associated with low bone mineral density in Turner syndrome: a multicenter prospective observational study von Ikegawa, Kento, Koga, Eri, Itonaga, Tomoyo, Sakakibara, Hideya, Kawai, Masanobu, Hasegawa, Yukihiro

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Sympathetic activation induces skeletal Fgf23 expression in a circadian rhythm-dependent manner von Kawai, Masanobu, Kinoshita, Saori, Shimba, Shigeki, Ozono, Keiichi, Michigami, Toshimi

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Growth-related skeletal changes and alterations in phosphate metabolism von Michigami, Toshimi, Tachikawa, Kanako, Yamazaki, Miwa, Nakanishi, Tatsuro, Kawai, Masanobu, Ozono, Keiichi

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Hypophosphatasia in Japan: ALPL Mutation Analysis in 98 Unrelated Patients von Michigami, Toshimi, Tachikawa, Kanako, Yamazaki, Miwa, Kawai, Masanobu, Kubota, Takuo, Ozono, Keiichi

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Very young children with Prader-Willi syndrome are refractory to growth hormone-associated decreases in free thyroxine levels von Konishi, Ayako, Koizumi, Mikiko, Etani, Yuri, Ida, Shinobu, Kawai, Masanobu

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Beta-human chorionic gonadotropin-producing neuroblastoma: an unrecognized cause of gonadotropin-independent precocious puberty von Maeyama, Takatoshi, Ichikawa, Chihiro, Okada, Yosuke, Sawada, Akihisa, Inoue, Masami, Takeuchi, Makoto, Soh, Hideki, Usui, Noriaki, Etani, Yuri, Kawai, Masanobu

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Nephrogenic diabetes insipidus caused by a novel missense variant (p.S127Y) in the AVPR2 gene von Maeyama, Takatoshi, Etani, Yuri, Nishigaki, Satsuki, Kawai, Masanobu

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A retrospective multicenter study of bone mineral density in adolescents and adults with Turner syndrome in Japan von Itonaga, Tomoyo, Koga, Eri, Nishigaki, Satsuki, Kawai, Masanobu, Sakakibara, Hideya, Hasegawa, Yukihiro

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