Keio University

Published papers

Hasegawa, Tomonobu

161-180 items (total 510)

Waist-to-height ratio centiles by age and sex for Japanese children based on the 1978-1981 cross-sectional national survey data.

Author
Inokuchi M, Matsuo N, Takayama J, Hasegawa T
Publication Title
Magazine name Int J Obes (London) Start Page 65 - End Page 70 (Publication Date)2016)
Authorship Category
Joint Work

Whole exome sequencing identified a novel COL2A1 mutation that causes mild spondylo-epiphyseal dysplasia mimicking autosomal dominat bracholmia.

Author
Takagi M, Shimizu M, Suzuki E, Shinohara H, Narumi S, Hasegawa T, Nishimura G, Hasegawa Y.
Publication Title
Magazine name Am J Med Genet Volume 170(Issue 3) Start Page 795 - End Page 798 (Publication Date)2016/03)

Frequencies of spontaneous breast development and spontaneous menarche in Turner syndrome in Japan.

Author
Tanaka T, Igarashi Y, Ozono K, Ohyama K, Ogawa M, Osada H, Onigata K, Kanzaki S, Kohno H, Seino Y, Takahashi H, Tajima T, Tachibana K, Tanaka H, Nishi Y, Hasegawa T, Fujita K, Yorifuji T, Horikawa R, Yokoya S.
Publication Title
Magazine name Clin Pediatr Endocrinol Start Page 3167 - End Page 3173 (Publication Date)2015)

Transient congenital hypothyroidism caused by compound heterozygous mutations affecting the NADPH-oxidase domain of DUOX2

Author
Yoshizawa-Ogasawara A, Abe K, Ogikubo S, Narumi S, Hasegawa T, Satoh M
Publication Title
Magazine name J Pediatr Endocrinol Metab (Publication Date)2015)

Turenr症候群とCAHの合併を認めた副腎偶発腫の一例

Author
岩橋泰幸、福岡秀規、中島進介、井口元三、本間桂子、長谷川奉延、小川渉、高橋裕
Publication Title
Volume 91(Issue Supple) Start Page 44 - End Page 46 (Publication Date)2015)

くり返す低血糖後にてんかんを発症した高インスリン血性低血糖症の1例

Author
福間真実、宮井健太郎、高木優樹、後藤正博、鳴海覚志、長谷川奉延、長谷川行洋
Publication Title
Start Page 139 - End Page 141 (Publication Date)2015)

小児における内分泌機能検査の注意点

Author
志村和浩、長谷川奉延
Publication Title
(Publication Date)2015)

原発性性腺機能低下症

Author
長谷川奉延
Publication Title
(Publication Date)2015)

TSH resistancerevisited.

Author
Narumi S, Hasegawa T
Publication Title
Magazine name Endocrine J Start Page 393 - End Page 398 (Publication Date)2015)
Authorship Category
Joint Work

Growth references for Japanese individuals with Noonan syndrome.

Author
Isojima T, Sakatsume S, Hasegawa T, Ogata T, Nakanishi T, Nagai T, Yokoya S
Publication Title
Magazine name Pediatr Res (Publication Date)2015)
Authorship Category
Joint Work

A novel mutation of THRB Gene in a Japanese family with resistance to thyroid hormone.

Author
Ito J, Narumi S, Nishizawa K, Kamimaki T, Hori N, Hasegawa T
Publication Title
Magazine name Clin Pediatr Endocrinol (Publication Date)2015)
Authorship Category
Joint Work

Combined GH and TSH deficiency in a Japanese patient with a novel frameshift mutation in IGSF1.

Author
Asakura Y, Abe K, Muroya K, Hanakawa J, Oto Y, Narumi S, Hasegawa T, Adachi M
Publication Title
Magazine name Hor Res Pediatr Start Page 349 - End Page 354 (Publication Date)2015)
Authorship Category
Joint Work

Human chorionic gonadotropin stimulation test in prepubertal children with micropenis can accurately predict Leydig cell function in pubertal or postpubertal adolescents.

Author
Ishii T. Matsuo N, Sato S, Ogata T, Tamai S, Anzo M, Kamimaki T, Sasaki G, Inokuchi M, Hori N, Amano N, Narumi S, Shibata H, Hasegawa T
Publication Title
Magazine name Hor Res Paediatr Start Page 305 - End Page 310 (Publication Date)2015)
Authorship Category
Joint Work

Clinical manifestations and enzymatic activities of mitochondrial respiratory chain complexes in Pearson marrow-pancreas syndrome with 3-methylglutaconic aciduria: a case report and literature review.

Author
Sato T, Muroya K, Hanakawa J, Asakura Y, Tanaka Y, Murayama K, Ohtake A, Hasegawa T, Adachi M
Publication Title
Magazine name Eur J Pediatr Start Page 1593 - End Page 1602 (Publication Date)2015)
Authorship Category
Joint Work

Polyostotic osteolysis and hypophosphatemic rickets with elevated serum fibroblast growth factor 23: a case report.

Author
Sato T, Muroya K, Asakura Y, Yachie A, Nishimura G, Aida N, Machida J, Tanaka Y, Hasegawa T, Adachi M
Publication Title
Magazine name Am J Med Genet Start Page 2430 - End Page 2434 (Publication Date)2015)
Authorship Category
Joint Work

A novel mutation Ser344Cys in FGFR3 causes achondroplasia with severe platyspondyly.

Author
Takagi M, Kouwaki M, Kawase K, Shinohara H, Hasegawa Y, Yamada T, Fujiwara I, Sawai H, Nishimura G, Hasegawa T
Publication Title
Magazine name Am J Med Genet Start Page 2851 - End Page 2854 (Publication Date)2015)
Authorship Category
Joint Work

A CYP3A4 inhibitor counterscts the mitotane-induced adrenal insufficiency and resistant hypertention in adrenocortical carcinoma.

Author
Minami I, Yoshimoto T, Tsujimoto K, Homma K, Hasegawa T, Ogawa Y
Publication Title
Magazine name AACE Clin Case Reports (Publication Date)2015)
Authorship Category
Joint Work

Severe osteogenesis imperfect caused by double substitutions of triple helical glycine residues in COL1A2.

Author
Takagi M, Shinohara H, Narumi S, Nishimura G, Hasegawa Y, Hasegawa T
Publication Title
Magazine name Am J Med Genet A Start Page 1627 - End Page 1631 (Publication Date)2015)
Authorship Category
Joint Work

A case with neonatal hyperinsulinemic hypoglycemia: It is a characteristic complication of Sotos syndrome.

Author
Nakamura Y, Takagi M, Yoshihashi H, Miura M, Narumi S, Hasegawa T, Miyake Y, Hasegawa Y
Publication Title
Magazine name Am J Med Genet Start Page 1627 - End Page 1631 (Publication Date)2015)
Authorship Category
Joint Work

高インスリン血性低血糖症の診断と治療ガイドライン

Author
長谷川奉延、田中敏章、神崎晋、杉原茂孝、横谷進、田中弘之、原田正平、藤枝憲二
Publication Title
Start Page 1472 - End Page 1474 (Publication Date)2006)