Early growth hormone treatment accelerates delayed onset of puberty in patients with growth hormone deficiency von Tanaka, Toshiaki, Soneda, Shun, Sato, Naoko, Kishi, Kentaro, Noda, Masahiro, Ogasawara, Atsuko

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Clinical practice guidelines for congenital hyperinsulinism von Yorifuji, Tohru, Horikawa, Reiko, Hasegawa, Tomonobu, Adachi, Masanori, Soneda, Shun, Minagawa, Masanori, Ida, Shinobu, Yonekura, Takeo, Kinoshita, Yoshiaki, Kanamori, Yutaka, Kitagawa, Hiroaki, Shinkai, Masato, Sasaki, Hideyuki, Nio, Masaki, (on behalf of The Japanese Society for Pediatric Endocrinology and The Japanese Society of Pediatric Surgeons)

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Increasing secular trends in height and obesity in children with type 1 diabetes: JSGIT cohort von Mochizuki, Mie, Ito, Yoshiya, Yokomichi, Hiroshi, Kikuchi, Toru, Soneda, Shun, Musha, Ikuma, Anzou, Makoto, Kobayashi, Koji, Matsuo, Kumihiro, Sugihara, Shigetaka, Sasaki, Nozomu, Matsuura, Nobuo, Amemiya, Shin

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Retrospective study of the renal function using estimated glomerular filtration rate and congenital anomalies of the kidney‐urinary tract in pediatric Turner syndrome von Izumita, Yukie, Nishigaki, Satsuki, Satoh, Mari, Takubo, Noriyuki, Numakura, Chikahiko, Takahashi, Ikuko, Soneda, Shun, Abe, Yoshifusa, Kamasaki, Hotaka, Ohtsu, Yoshiaki, Igaki, Junko, Hasegawa, Yukihiro, Nagasaki, Keisuke

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SLC25A13 gene analysis in citrin deficiency: sixteen novel mutations in East Asian patients, and the mutation distribution in a large pediatric cohort in China von Song, Yuan-Zong, Zhang, Zhan-Hui, Lin, Wei-Xia, Zhao, Xin-Jing, Deng, Mei, Ma, Yan-Li, Guo, Li, Chen, Feng-Ping, Long, Xiao-Ling, He, Xiang-Ling, Sunada, Yoshihide, Soneda, Shun, Nakatomi, Akiko, Dateki, Sumito, Ngu, Lock-Hock, Kobayashi, Keiko, Saheki, Takeyori

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Mutation spectrum and phenotypic variation in nine patients with SOX2 abnormalities von Suzuki, Junichi, Azuma, Noriyuki, Dateki, Sumito, Soneda, Shun, Muroya, Koji, Yamamoto, Yukiyo, Saito, Reiko, Sano, Shinichiro, Nagai, Toshiro, Wada, Hiroshi, Endo, Akira, Urakami, Tatsuhiko, Ogata, Tsutomu, Fukami, Maki

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Rare pseudoautosomal copy-number variations involving SHOX and/or its flanking regions in individuals with and without short stature von Fukami, Maki, Naiki, Yasuhiro, Muroya, Koji, Hamajima, Takashi, Soneda, Shun, Horikawa, Reiko, Jinno, Tomoko, Katsumi, Momori, Nakamura, Akie, Asakura, Yumi, Adachi, Masanori, Ogata, Tsutomu, Kanzaki, Susumu

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

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Systematic molecular analyses of SHOX in Japanese patients with idiopathic short stature and Leri-Weill dyschondrosteosis von Shima, Hirohito, Tanaka, Toshiaki, Kamimaki, Tsutomu, Dateki, Sumito, Muroya, Koji, Horikawa, Reiko, Kanno, Junko, Adachi, Masanori, Naiki, Yasuhiro, Tanaka, Hiroyuki, Mabe, Hiroyo, Yagasaki, Hideaki, Kure, Shigeo, Matsubara, Yoichi, Tajima, Toshihiro, Kashimada, Kenichi, Ishii, Tomohiro, Asakura, Yumi, Fujiwara, Ikuma, Soneda, Shun, Nagasaki, Keisuke, Hamajima, Takashi, Kanzaki, Susumu, Jinno, Tomoko, Ogata, Tsutomu, Fukami, Maki

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Proximal Promoter of the Cytochrome P450 Oxidoreductase Gene: Identification of Microdeletions Involving the Untranslated Exon 1 and Critical Function of the SP1 Binding Sites von Soneda, Shun, Yazawa, Takashi, Fukami, Maki, Adachi, Masanori, Mizota, Michiyo, Fujieda, Kenji, Miyamoto, Kaoru, Ogata, Tsutomu

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Acroscyphodysplasia as a phenotypic variation of pseudohypoparathyroidism and acrodysostosis type 2 von Mitsui, Toshikatsu, Kim, Ok-Hwa, Hall, Christine M., Offiah, Amaka, Johnson, Diana, Jin, Dong-Kyu, Toh, Teck-Hock, Soneda, Shun, Keino, Dai, Matsubayashi, Shohei, Ishii, Tomohiro, Nishimura, Gen, Hasegawa, Tomonobu

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Disorders of sex development cases diagnosed at inguinal hernia repair von Manabe, Shutaro, Furuta, Shigeyuki, Sato, Hideaki, Soneda, Shun, Kitagawa, Hiroaki

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Clinical practice guidelines for congenital hyperinsulinism von Tohru Yorifuji, Reiko Horikawa, Tomonobu Hasegawa, Masanori Adachi, Shun Soneda, Masanori Minagawa, Shinobu Ida, Takeo Yonekura, Yoshiaki Kinoshita, Yutaka Kanamori, Hiroaki Kitagawa, Masato Shinkai, Hideyuki Sasaki, Masaki Nio, on behalf of The Japanese Society for Pediatric Endocrinology and The Japanese Society of Pediatric Surgeons

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Usefulness of insulin detemir in Japanese children with type 1 diabetes von Jinno, Kazuhiko, Urakami, Tatsuhiko, Horikawa, Reiko, Kawamura, Tomoyuki, Kikuchi, Nobuyuki, Kikuchi, Tohru, Kizu, Rika, Kosaka, Kitaro, Mizuno, Haruo, Mochizuki, Takahiro, Nishii, Aki, Ohki, Yukashi, Soneda, Shun, Sugihara, Shigetaka, Tatematsu, Toshi, Amemiya, Shin

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Comprehensive study on central precocious puberty: molecular and clinical analyses in 90 patients von Narusawa, Hiromune, Ogawa, Tomoe, Yagasaki, Hideaki, Nagasaki, Keisuke, Urakawa, Tatsuki, Saito, Tomohiro, Soneda, Shun, Kinjo, Saori, Sano, Shinichiro, Mamada, Mitsukazu, Terashita, Shintaro, Dateki, Sumito, Narumi, Satoshi, Naiki, Yasuhiro, Horikawa, Reiko, Ogata, Tsutomu, Fukami, Maki, Kagami, Masayo

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A case report: Primary extragonadal yolk sac tumor of penile shaft in a 2‐year‐old child von Nakazawa, Ryuto, Soneda, Shun, Kinoshita, Akitoshi, Kitagawa, Hiroaki, Koike, Junki, Chikaraishi, Tatsuya

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Early growth hormone treatment accelerates delayed onset of puberty in patients with growth hormone deficiency von Tanaka, Toshiaki, Soneda, Shun, Sato, Naoko, Kishi, Kentaro, Noda, Masahiro, Ogasawara, Atsuko

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Incidence and Risk Factors for Adrenal Crisis in Pediatric-onset Adrenal Insufficiency: A Prospective Study von Hosokawa, Mayumi, Ichihashi, Yosuke, Sato, Yasunori, Shibata, Nao, Nagasaki, Keisuke, Ikegawa, Kento, Hasegawa, Yukihiro, Hamajima, Takashi, Nagamatsu, Fusa, Suzuki, Shigeru, Numakura, Chikahiko, Amano, Naoko, Sasaki, Goro, Nagahara, Keiko, Soneda, Shun, Ariyasu, Daisuke, Maeda, Miwako, Kamasaki, Hotaka, Aso, Keiko, Hasegawa, Tomonobu, Ishii, Tomohiro

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Association of Micropenis with Pro185Ala Polymorphism of the Gene for Aryl Hydrocarbon Receptor Repressor Involved in Dioxin Signaling von SONEDA, Shun, FUKAMI, Maki, FUJIMOTO, Masatoshi, HASEGAWA, Tomonobu, KOITABASHI, Yasushi, OGATA, Tsutomu

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Once-Weekly Somapacitan vs Daily GH in Children With GH Deficiency: Results From a Randomized Phase 2 Trial von Sävendahl, Lars, Battelino, Tadej, Brod, Meryl, Højby Rasmussen, Michael, Horikawa, Reiko, Juul, Rasmus Vestergaard, Saenger, Paul

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