Published papers
Hasegawa, Tomonobu
341-360 items (total 510)
A homozygous mutation of the nicotinamide nucleotide transhydrogenase gene in a Japanese patient with familial glucocorticoid deficiency.
- Author
- Yamaguchi R, Kato F, Hasegawa T, Katsumata N, Fukami M, Matsui T, Nagasaki K, Ogata T
- Publication Title
- Magazine name Endcrine J Start Page 855 - End Page 859 (Publication Date）2013）
- Authorship Category
- Joint Work
An observational study of the effectiveness and safety of growth hormone (HUmatrope) treatment in Japanese children with growth hormone deficiency or turner syndrome.
- Author
- Tai S, Tanaka T, Hasegawa T, Ozono K, Tanaka H, Kanzaki S, Yokoya S, Fujieda K, Chihara K, Seino Y
- Publication Title
- Magazine name Endcr J Start Page 57 - End Page 64 (Publication Date）2013）
- Authorship Category
- Joint Work
Quantitative and Sensitive Detection of GNAS Mutations Causing McCune-Albright Syndrome with Next Generation Sequencing.
- Author
- Narumi S, Matsuo K, Ishii T, Tanahashi Y, Hasegawa T
- Publication Title
- Magazine name PLos One Start Page e60525 (Publication Date）2013）
- Authorship Category
- Joint Work
Spousal choice by height in as urban middle-class Japanese
- Author
- Uchida K, Matsuo N, Hori N, Hasegawa T, Takahashi T
- Publication Title
- Magazine name Hum Biol Start Page 619 - End Page 621 (Publication Date）2013）
- Authorship Category
- Joint Work
Delayed onset congenital hypothyroidism in a patient with DUOX2 mutations and maternal iodine excess.
- Author
- Kasahara T, Narumi S, Okasora K, Takaya R, Tamai H, Hasegawa T
- Publication Title
- Magazine name Am J Med Genet A Start Page 214 - End Page 217 (Publication Date）2013）
- Authorship Category
- Joint Work
Reference intervals of urinary free adrenal steroids in Japanese newborn infants using stable isotope dilution - gas chromatography / mass spectrometry.
- Author
- Koyama Y, Homma K, Miwa M, Ikeda K, Murata M, Hasegawa T
- Publication Title
- Magazine name Clin Chem Acta Start Page 302 - End Page 305 (Publication Date）2013）
- Authorship Category
- Joint Work
A report of two novel NR5A1 mutation families: possible clinical phenotype of psychiatric symptoms of anxiety and/or depression.
- Author
- Suwanai SA, Ishii T, Haruna H, Yamataka A, Narumi S, Fukuzawa R, Ogata T, Hasegawa T
- Publication Title
- Magazine name Clin Endocrinol Start Page 957 - End Page 965 (Publication Date）2013）
- Authorship Category
- Joint Work
Two neonatal cholestasis patients with mutations in the SRD5B1 (AKR1D1) gene: diagnosis and bile acid profiles during chenodeoxycholic acid treatment.
- Author
- Seki Y, Mizuochi T, Kimura A, Takahashi T, Ohtake A, Hayashi S-i, Morimura T, Ohno Y, Hoshina T, Ihara K, Takei H, Nittono H, Kurosawa T, Homma K, Hasegawa T, Matsuishi T
- Publication Title
- Magazine name J Inherit Metab Dis Start Page 565 - End Page 573 (Publication Date）2013）
- Authorship Category
- Joint Work
Congenital hypothyroidism caused by a novel mutation of the dual oxidase2 (DUOX2) gene.
- Author
- Yoshizawa-Ogasawara A, Ogikubo S, Satoh M, Narumi S, Hasegawa T
- Publication Title
- Magazine name J Pediatr Endor Met Start Page 45 - End Page 52 (Publication Date）2013）
- Authorship Category
- Joint Work
被虐待児症候群と鑑別が困難であった骨系統疾患の2例
- Author
- 今嶋由香理、北野元裕、上田孝文、岡本伸彦、髙木優樹、長谷川奉延
- Publication Title
- Start Page 33 - End Page 36 (Publication Date）2012）
新生児マス・スクリーニング検査の17α水酸化プロゲステロン（17-OHP）高値を契機に、内分泌学的検査をもとに診断されたACTH非依存性Cushing症候群の1例
- Author
- 12. 橘田一輝、田久保憲行、昆信也、大津成之、風張眞由美、横田行史、笹野公伸、本間桂子、長谷川奉延、石井正浩
- Publication Title
- Start Page 212 - End Page 216 (Publication Date）2012）
未治療成人17α水酸化酵素欠損症患者の遺伝的、内分泌学的解析
- Author
- 201. 植田洋平、渡邊知一、臼井健、垣田真似子、中谷理恵子、中尾佳奈子、難波多拳、立木美香、田上哲也、成瀬光栄、金子恵一、本間桂子、長谷川奉延、島津章
- Publication Title
- Volume 90(Issue Suppl) Start Page 72 - End Page 74 (Publication Date）2014）
成長ホルモン分泌不全性低身長症
- Author
- 上牧務、長谷川奉延
- Publication Title
- (Publication Date）2014）
下垂体疾患のトランジション
- Author
- 安蔵慎、長谷川奉延
- Publication Title
- (Publication Date）2014）
性腺機能低下症
- Author
- 吉田理恵、長谷川奉延
- Publication Title
- Start Page 1599 - End Page 1601 (Publication Date）2014）
外陰部異常のみかた
- Author
- 佐々木悟郎、長谷川奉延
- Publication Title
- Start Page 859 - End Page 863 (Publication Date）2014）
肺炎球菌結合型ワクチンと子宮頸がん予防ワクチン
- Author
- 長谷川奉延、新庄正宜
- Publication Title
- Start Page 468 - End Page 469 (Publication Date）2014）
Antley-Bixler症候群
- Author
- 細川真弓、長谷川奉延
- Publication Title
- Start Page 489 - End Page 491 (Publication Date）2014）
性分化疾患
- Author
- 林美恵、長谷川奉延
- Publication Title
- Start Page 602 - End Page 603 (Publication Date）2014）
C-type natriuretic peptide (CNP) plasma levels are elevated in subjects with achondroplasia, hypochondroplasia, and thanatophoric dysplasia.
- Author
- Olney RC, Prickett TCR, Espiner EA, Mackenzie WG, Duker A, Ditro C, Zabel B, Hasegawa T, Kitoh H, Aylsworth AS, Bober MB
- Publication Title
- Magazine name J Clin Endocrinol Metab Start Page E355 - End Page 359 (Publication Date）2014）
- Authorship Category
- Joint Work