Published papers
Hasegawa, Tomonobu
101-120 items (total 510)
Population Pharmacokinetics of Diazoxide in Children with Hyperinsulinemic Hypoglycemia.
- Author
- Kizu R, Nishimura K, Sato R, Kosaki K, Tanaka T, Tanigawara Y, Hasegawa T.
- Publication Title
- Magazine name Hor Res Peadiatr Start Page 316-323 (Publication Date)2017)
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- Joint Work
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- Research paper (scientific journal)
- Peer-review Status
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Mild thyroid peroxidase deficiency caused by TPO mutations with residual activir: Correlation between clinical phenotypes and enzymatic activity.
- Author
- Narumi S, Fox LA, Fukudome K, Sakaguchi Z, Sugisawa C, Abe K, Kameyama K, Hasegawa T.
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- Magazine name Endocr J Start Page 1087-1097 (Publication Date)2017)
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- Joint Work
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- Research paper (scientific journal)
- Peer-review Status
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Discordant fetal phenotype of hypophosphatasia in two siblings.
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- Ikenoue S, Miyakoshi K, Ishii T, Sato Y, Otani T, Akiba Y, Kasuga Y, Ochiai D, Matsumoto T, Matsuzaki Y, Tachikawa K, Michigami T, Nishimura G, Ikeda K, Hasegawa T, Tanaka M.
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- Magazine name Am J Med Genet A Start Page 171-174 (Publication Date)2017)
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- Joint Work
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- Research paper (scientific journal)
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Adenocorical cartinoma characterized by gynecomastia: A case report.
- Author
- Takeuchi T, Yoto Y, Ishii A, Tsugawa T, Yamamoto M, Hori T, Kamasaki H, Nogami K, Oda T, Nui A, Kimura S, Yamagishi T, Homma K, Hasegawa T, Fukami M, Watanabe Y, Sasamoto H, Tsutsumi H.
- Publication Title
- Magazine name Clin Pediatr Endocrinol Start Page 9-18 (Publication Date)2018)
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- Joint Work
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- Research paper (scientific journal)
- Peer-review Status
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Association between monoallelic TSHR mutations and congenital hypothyroidism: a statistical approach.
- Author
- Abe K, Narumi S, Suwanai AS, Adachi M, Muroya K, Asakura Y, Nagasaki K, Abe T, Hasegawa T.
- Publication Title
- Magazine name Eur J Endocrinol Start Page 137-144 (Publication Date)2018)
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- Joint Work
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- Research paper (scientific journal)
- Peer-review Status
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WHO 2006 Child Growth Standards overestimate short stature and underestimate overweight in Japanese children.
- Author
- Inokuchi M, Matsuo N, Takayama JI, Hasegawa T.
- Publication Title
- Magazine name J Pediatr Endocrinol Metab Start Page 33-38 (Publication Date)2018)
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- Joint Work
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- Research paper (scientific journal)
- Peer-review Status
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Prevalence of central fatness in 1992-1994: 40% of Japanese boys 6-17 years.
- Author
- Inokuchi M, Matsuo N, Takayama JI, Hasegawa T.
- Publication Title
- Magazine name Endocrine J Start Page 213-220 (Publication Date)2018)
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- Joint Work
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- Research paper (scientific journal)
- Peer-review Status
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Serum 25-hydroxyvitamin D3 levels of one-month-old term infants in Tokyo using liquid chromatography tandem mass spectrometry.
- Author
- Hara K, Koyama Y, Wada Y, Ikeda K, Hasegawa T.
- Publication Title
- Magazine name Acta Paediatr Start Page 532-533 (Publication Date)2018)
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- Joint Work
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- Research paper (scientific journal)
- Peer-review Status
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Longitudinal serum and urine steroid metabolite profiling in a 46,XY infant with prenatally identified POR deficiency.
- Author
- Ono H, Numakura C, Homma K, Hasegawa T, Tsutsumi S, Kato F, Fujisawa Y, Fukami M, Ogata T.
- Publication Title
- Magazine name J Steroid Biochem Mol Biol Start Page 177-184 (Publication Date)2018)
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- Joint Work
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- Research paper (scientific journal)
- Peer-review Status
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A pediatric case of pheochromocytoma without apparent hypertension associated with von Hippel-Lindau disease.
- Author
- Igaki J, Nishi A, Sato T, Hasegawa T.
- Publication Title
- Magazine name Clin Pediatr Endocrinol Start Page 87-93 (Publication Date)2018)
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- Joint Work
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- Research paper (scientific journal)
- Peer-review Status
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Identification of a nonclassic TSH resistance patient with compound heterozygous TSHR mutations (p.[R109Q];[R450H]) and functional characterization of the mutant receptors.
- Author
- Sugisawa C, Abe K, Sunaga Y, Taniyama M, Hasegawa T, Narumi S.
- Publication Title
- Magazine name Clin Pediatr Endocrinol Start Page 123-130 (Publication Date)2018)
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- Joint Work
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- Research paper (scientific journal)
- Peer-review Status
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Trismus-pseudocamptodactyly syndrome with bilateral hypoplastic mandibular condyles and shallow mandibular fossa: A case report.
- Author
- Kusako C, Hori N, Izawa K, Kosaki R, Nishimura G, Hasegawa T.
- Publication Title
- Magazine name Oral Science International Start Page 90-92 (Publication Date)2018)
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- Joint Work
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- Research paper (scientific journal)
- Peer-review Status
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Co-administration of the CYP3A4 inhibitor diltiazem counterscts the mitotane-induced clearance of glucocorticoids and antihypertensives in a patient with adrenocortical carcinoma.
- Author
- Minami I, Yoshimoto T, Tsujimoto K, Homma K, Hasegawa T, Ogawa Y.
- Publication Title
- Magazine name AACE Clin Case Reports Start Page e36-e40 (Publication Date)2016)
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- Joint Work
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- Research paper (scientific journal)
- Peer-review Status
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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 Start Page 19-22 (Publication Date)2016)
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- Joint Work
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- Research paper (scientific journal)
- Peer-review Status
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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 Start Page 543-548 (Publication Date)2016)
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- Joint Work
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- Research paper (scientific journal)
- Peer-review Status
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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 Start Page 363-371 (Publication Date)2016)
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- Joint Work
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- Research paper (scientific journal)
- Peer-review Status
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Criteria for Radiological Diagnosis of Hypochondroplasia in Neonates.
- Author
- Saito T, Nagasaki K, Nishimura G, Wada M, Nyuzuki H, Takagi M, Hasegawa T, Amano N, Murotsuki J, Sawai H, Yamada T, Sato S, Saitoh A.
- Publication Title
- Magazine name Pediatr Radiol Start Page 513-518 (Publication Date)2016)
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- Joint Work
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- Research paper (scientific journal)
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Classic and non-classic 21-hydroxylase deficiency can be discriminated from P450 oxidoreductase deficiency in Japanese infants by urinary steroid metabolites.
- Author
- Koyama Y, Homma K, Fukami M, Miwa M, Ikeda K, Ogata T, Murata M, Hasegawa T.
- Publication Title
- Magazine name Clin Pediatr Endocrinol Start Page 37-44 (Publication Date)2016)
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- Joint Work
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- Research paper (scientific journal)
- Peer-review Status
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A novel mutation in HESX1 causes combined pituitary hormone deficiency without septo optic dysplasia phenotypes.
- Author
- Takagi M, Takahashi M, Ohtsu Y, Sato T, Narumi S, Arakawa H, Hasegawa T.
- Publication Title
- Magazine name Endocrine J Start Page 405-410 (Publication Date)2016)
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- Joint Work
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- Research paper (scientific journal)
- Peer-review Status
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A case of mature teratoma with a falsely high serum estradiol value measured with immunoassay.
- Author
- Hosokawa M, Shibata H, Ishii T, Fujino A, Kuroda T, kosaki K, Kameyama K, Hasegawa T.
- Publication Title
- Magazine name J Pediatr Endocrinol Metab Start Page 737-739 (Publication Date)2016)
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- Joint Work
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- Research paper (scientific journal)
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