Presentations -
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Genetic and imaging analyses of sibling cases with congenital hypothyroidism revealed the distinct clinical courses despite the presence of the identical mutation.
Koizumi M, Onuma S, Nakacho M, Syoji Y, Kawai M, Etani Y, Ida S, Sugisawa C, Abe K, Narumi S, Hasegawa T.
The 9th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society / The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology (Tokyo) ,
2016.11,Oral presentation (general)
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Mutation frequency in Japanese male patients with severe form of hypogonadotropic hypogonadism.
Sato T, Narumi S, Ishii T, Muroya K, Asakura Y, Takagi M, Minagawa M, Suzuki H, Sugisawa C, Saito J, Hasegawa Y, Adachi M, Hasegawa T.
The 9th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society / The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology (Tokyo) ,
2016.11,Oral presentation (general)
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Detection of somatic activating GNAS mutations in girls with isolated autonomous ovarian cyst by next generation sequencing.
Shibata H, Narumi S, Ishii T, Muroya K, Asakura Y, Adachi M, Sasaki G, Shibazaki T, Hara Y, Hasegawa T.
The 9th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society / The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology (Tokyo) ,
2016.11,Oral presentation (general)
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FGFR1 mutations ih four patients with congenital hypogonadotropic hypogonadism and split-hand/foot malformation: implications for the FGFR1 proximal promoter region.
Ohtaka K, Fujisawa Y, Yamaguchi R, Kato F, Yagasaki H, Miyoshi T, Hasegawa Y, Hasegawa T, Miyoshi H, Takada F, Katsumi M, Fukami M, Ogata T.
The 9th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society / The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology (Tokyo) ,
2016.11,Oral presentation (general)
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Incidence of type 2 diabetes mellitus an neoplasm in growth hormone treated children in Japan.
Yokoya S, Hasegawa T, Ozono K, Tanaka H, Kanzaki S, Tanaka T, Chihara K, Jia N, Child CJ, Iwamoto N, Seino Y.
The 9th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society / The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology (Tokyo) ,
2016.11,Poster presentation
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Practical growth charts for Japanese children with Noonan syndrome.
Isojima T, Sakazume S, Hasegawa T, Ogata T, Nakanishi T, Nagai T, Yokoya S.
The 9th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society / The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology (Tokyo) ,
2016.11,Poster presentation
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A novel de novo germline mutation Glu40Lys in AKT3 causes megalencephaly with growth hormone deficiency.
Nagahara K, Takagi M, Fujii T, Nishimura G, Kato M, Dobashi K, Itabashi K, Narumi S, Hasegawa T.
The 9th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society / The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology (Tokyo) ,
2016.11,Poster presentation
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Mild thyroid peroxidase defect: A case series.
Narumi S, Abe K, Fox LA, Kamimura M, Kanno J, Fujiwara I, Fukudome K, Sakaguchi Z, Fukami M, Hasegawa T.
The 9th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society / The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology (Tokyo) ,
2016.11,Poster presentation
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Rapid growth and early metastasis of papillary thyroid carcinoma in an adolescent girl with Graves’ disease.
Shimura K, Ishii T, Shibata H, Hoshino K, Kuroda T, Kameyama K, Mitsutake N, Sugino K, Yoshimura JN, Hasegawa T.
The 9th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society / The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology (Tokyo) ,
2016.11,Poster presentation
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Long-term clinical course in three patients with MAMLD1 mutations.
Fujisawa Y, Fukami M, Hasegawa T, Uematsu A, Muroya K, Ogata T.
The 9th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society / The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology (Tokyo) ,
2016.11,Poster presentation
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Characterization of androgen production in a genetic male infant with prenatally diagnosed POR deficiency.
Ono H, Numakura C, Tsutsumi S, Homma K, Hasegawa T, Kato F, Ogata T.
The 9th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society / The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology (Tokyo) ,
2016.11,Poster presentation
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Two brothers with ATRX mutation having micropenis without other features of ATR-X syndrome.
Eguchi M, Yamamoto Y, Saito R, Goto M, Araki S, Kubo K, Kawagoe R, Kawada Y, Kusuhara K, Sato T, Narumi S, Hasegawa T.
The 9th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society / The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology (Tokyo) ,
2016.11,Poster presentation
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A case of partial androgen insensitivity syndrome caused by a novel mutation of the AR gene.
Iwahashi M, Ozawa A, Sato T, Narumi S, Hasegawa T, Miyata I.
The 9th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society / The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology (Tokyo) ,
2016.11,Poster presentation
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Serum 25-hydroxyvitamin D3 levels of one-month-old term infants in Tokyo using liquid chromatography tandem mass spectrometry.
Hara K, Ikeda K, Hasegawa T, Koyama Y, Wada Y.
The 9th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society / The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology (Tokyo) ,
2016.11,Poster presentation
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Fanconi syndrome in a patient with McCune-Albright syndrome.
Nogayama T, Shibata H, Matsumura K, Matsuura H, Hara Y, Kosho T, Narumi S, Ishii T, Awazu M, Hasegawa T.
The 9th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society / The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology (Tokyo) ,
2016.11,Poster presentation
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TSH受容体細胞内ドメインの系統的変異導入研究：どのようなナンセンス/フレームシフトバリアントが機能低下をきたすか？
杉澤千穂、阿部清美、谷山松雄、長谷川奉延、鳴海覚志
第59回日本甲状腺学会学術集会 (東京) ,
2016.11,Oral presentation (general)
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頸部の炎症を契機に発見され、血流豊富な甲状腺結節を伴う甲状腺中毒症の一例
乃村元子、小林佐紀子、栗原勲、石井智弘、福島裕之、長谷川奉延、伊藤裕
第59回日本甲状腺学会学術集会 (東京) ,
2016.11,Poster presentation
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日本人小児標準骨年齢アトラスの作成のための骨年齢レントゲンの選択
田中敏章、横谷進、加藤則子、伊藤善也、立花克彦、杉原茂孝、長谷川奉延、大関武彦、村田光範、原光彦、有阪治、菊池透、高井省三、佐藤亨至、佐藤真理、篠田謙一
第27回日本成長学会学綬ｔ集会 (米子) ,
2016.10,Oral presentation (general)
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標準的な成長をしている小児のデータを用いた縦断的成長曲線・成長率曲線の作成
磯島豪、田中敏章、横谷進、加藤則子、伊藤善也、立花克彦、杉原茂孝、長谷川奉延、大関武彦、村田光範、原光彦、有阪治、菊池透、高井省三、佐藤亨至、佐藤真理、篠田謙一
第27回日本成長学会学綬ｔ集会 (米子) ,
2016.10,Oral presentation (general)
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日本人小児arm span, arm span身長比およびarm span身長差の基準値作成
野ヶ山泰介、井ノ口美香子、長谷川奉延
第27回日本成長学会学綬ｔ集会 (米子) ,
2016.10,Oral presentation (general)