Increasing secular trends in height and obesity in children with type 1 diabetes: JSGIT cohort
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
Published in PloS one (23.11.2020)
Published in PloS one (23.11.2020)
Get full text
Journal Article
Clinical practice guidelines for congenital hyperinsulinism
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)
Published in Clinical Pediatric Endocrinology (01.01.2017)
Published in Clinical Pediatric Endocrinology (01.01.2017)
Get full text
Journal Article
Retrospective study of the renal function using estimated glomerular filtration rate and congenital anomalies of the kidney‐urinary tract in pediatric Turner syndrome
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
Published in Congenital anomalies (01.11.2020)
Published in Congenital anomalies (01.11.2020)
Get full text
Journal Article
SLC25A13 gene analysis in citrin deficiency: sixteen novel mutations in East Asian patients, and the mutation distribution in a large pediatric cohort in China
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
Published in PloS one (19.09.2013)
Published in PloS one (19.09.2013)
Get full text
Journal Article
Mutation spectrum and phenotypic variation in nine patients with SOX2 abnormalities
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
Published in Journal of human genetics (01.06.2014)
Published in Journal of human genetics (01.06.2014)
Get full text
Journal Article
Rare pseudoautosomal copy-number variations involving SHOX and/or its flanking regions in individuals with and without short stature
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
Published in Journal of human genetics (01.09.2015)
Published in Journal of human genetics (01.09.2015)
Get full text
Journal Article
Systematic molecular analyses of SHOX in Japanese patients with idiopathic short stature and Leri-Weill dyschondrosteosis
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
Published in Journal of human genetics (01.07.2016)
Published in Journal of human genetics (01.07.2016)
Get full text
Journal Article
(Epi)genetic defects of MKRN3 are rare in Asian patients with central precocious puberty
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 Human genome variation (21.01.2019)
Published in Human genome variation (21.01.2019)
Get full text
Journal Article
Proximal Promoter of the Cytochrome P450 Oxidoreductase Gene: Identification of Microdeletions Involving the Untranslated Exon 1 and Critical Function of the SP1 Binding Sites
Soneda, Shun, Yazawa, Takashi, Fukami, Maki, Adachi, Masanori, Mizota, Michiyo, Fujieda, Kenji, Miyamoto, Kaoru, Ogata, Tsutomu
Published in The journal of clinical endocrinology and metabolism (01.11.2011)
Published in The journal of clinical endocrinology and metabolism (01.11.2011)
Get full text
Journal Article
Acroscyphodysplasia as a phenotypic variation of pseudohypoparathyroidism and acrodysostosis type 2
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
Published in American journal of medical genetics. Part A (01.10.2014)
Published in American journal of medical genetics. Part A (01.10.2014)
Get full text
Journal Article
Disorders of sex development cases diagnosed at inguinal hernia repair
Manabe, Shutaro, Furuta, Shigeyuki, Sato, Hideaki, Soneda, Shun, Kitagawa, Hiroaki
Published in Journal of pediatric surgery case reports (01.09.2017)
Published in Journal of pediatric surgery case reports (01.09.2017)
Get full text
Journal Article
Clinical practice guidelines for congenital hyperinsulinism
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
Published in Clinical Pediatric Endocrinology (01.07.2017)
Get full text
Published in Clinical Pediatric Endocrinology (01.07.2017)
Journal Article
Usefulness of insulin detemir in Japanese children with type 1 diabetes
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
Published in Pediatrics international (01.12.2012)
Published in Pediatrics international (01.12.2012)
Get full text
Journal Article
Association of Micropenis with Pro185Ala Polymorphism of the Gene for Aryl Hydrocarbon Receptor Repressor Involved in Dioxin Signaling
SONEDA, Shun, FUKAMI, Maki, FUJIMOTO, Masatoshi, HASEGAWA, Tomonobu, KOITABASHI, Yasushi, OGATA, Tsutomu
Published in Endocrine Journal (01.02.2005)
Published in Endocrine Journal (01.02.2005)
Get full text
Journal Article
Comparison of the effectiveness of prepubertal growth hormone treatment on height and predicted adult height in children with short stature born small for gestational age vs. with a growth hormone deficiency
Tanaka, Toshiaki, Soneda, Shun, Sato, Naoko, Kishi, Kentaro, Noda, Masahiro
Published in Journal of pediatric endocrinology & metabolism : JPEM (31.10.2024)
Published in Journal of pediatric endocrinology & metabolism : JPEM (31.10.2024)
Get full text
Journal Article
Comprehensive study on central precocious puberty: molecular and clinical analyses in 90 patients
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
Published in The journal of clinical endocrinology and metabolism (26.09.2024)
Published in The journal of clinical endocrinology and metabolism (26.09.2024)
Get more information
Journal Article