Papers - Hasegawa, Tomonobu
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A pediatric case of an insulinoma and a novel MEN1 mutation: the efficacy of the combination therapy of diazoxide and cornstarch.
Nakano S, Sato T, Hosokawa M, Takagi C, Yoshida F, Ishii T, Sato S, Hasegawa T.
Clin Pediatric Endocrinol 27 199 2018
Research paper (scientific journal), Joint Work, Accepted
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Trismus-pseudocamptodactyly syndrome with bilateral hypoplastic mandibular condyles and shallow mandibular fossa: A case report.
Kusako C, Hori N, Izawa K, Kosaki R, Nishimura G, Hasegawa T.
Oral Science International 15 90-92 2018
Research paper (scientific journal), Joint Work, Accepted
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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.
Sugisawa C, Abe K, Sunaga Y, Taniyama M, Hasegawa T, Narumi S.
Clin Pediatr Endocrinol 27 123-130 2018
Research paper (scientific journal), Joint Work, Accepted
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A pediatric case of pheochromocytoma without apparent hypertension associated with von Hippel-Lindau disease.
Igaki J, Nishi A, Sato T, Hasegawa T.
Clin Pediatr Endocrinol 27 87-93 2018
Research paper (scientific journal), Joint Work, Accepted
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Longitudinal serum and urine steroid metabolite profiling in a 46,XY infant with prenatally identified POR deficiency.
Ono H, Numakura C, Homma K, Hasegawa T, Tsutsumi S, Kato F, Fujisawa Y, Fukami M, Ogata T.
J Steroid Biochem Mol Biol 178 177-184 2018
Research paper (scientific journal), Joint Work, Accepted
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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, Koyama Y, Wada Y, Ikeda K, Hasegawa T.
Acta Paediatr 107 532-533 2018
Research paper (scientific journal), Joint Work, Accepted
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Prevalence of central fatness in 1992-1994: 40% of Japanese boys 6-17 years.
Inokuchi M, Matsuo N, Takayama JI, Hasegawa T.
Endocrine J 65 213-220 2018
Research paper (scientific journal), Joint Work, Accepted
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WHO 2006 Child Growth Standards overestimate short stature and underestimate overweight in Japanese children.
Inokuchi M, Matsuo N, Takayama JI, Hasegawa T.
J Pediatr Endocrinol Metab 26 33-38 2018
Research paper (scientific journal), Joint Work, Accepted
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Association between monoallelic TSHR mutations and congenital hypothyroidism: a statistical approach.
Abe K, Narumi S, Suwanai AS, Adachi M, Muroya K, Asakura Y, Nagasaki K, Abe T, Hasegawa T.
Eur J Endocrinol 178 137-144 2018
Research paper (scientific journal), Joint Work, Accepted
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A novel heterozygous intronic mutation in POU1F1 is associated with combined pituitary hormone deficiency.
Takagi M, Kamasaki H, Yagi H, Fukuzawa R, Narumi S, Hasegawa T.
Endocrine J 64 229-234 2017
Research paper (scientific journal), Joint Work, Accepted
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Discordant fetal phenotype of hypophosphatasia in two siblings.
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.
Am J Med Genet A 176 171-174 2017
Research paper (scientific journal), Joint Work, Accepted
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Mild thyroid peroxidase deficiency caused by TPO mutations with residual activir: Correlation between clinical phenotypes and enzymatic activity.
Narumi S, Fox LA, Fukudome K, Sakaguchi Z, Sugisawa C, Abe K, Kameyama K, Hasegawa T.
Endocr J 64 1087-1097 2017
Research paper (scientific journal), Joint Work, Accepted
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Population Pharmacokinetics of Diazoxide in Children with Hyperinsulinemic Hypoglycemia.
Kizu R, Nishimura K, Sato R, Kosaki K, Tanaka T, Tanigawara Y, Hasegawa T.
Hor Res Peadiatr 88 316-323 2017
Research paper (scientific journal), Joint Work, Accepted
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Incidence of diabetes mellitus and neoplasia in Japanese short-statured children treated with growth hormonr in the Genetics and neuroendocrinology of short stature international study (GeNeSIS)
Yokoya S, Hasegawa T, Ozono K, Tanaka H, Kanzaki S, Tanaka T, Chihara K, Jia N, Child CJ, Ihara K, Funai J, Iwamoto N, Seino Y.
Clin Pediatr Endocrinol 26 229-241 2017
Research paper (scientific journal), Joint Work, Accepted
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Novel compound heterozygous mutations identified by whole exome sequencing in a Japanese patient with geroderma osteodysplastica.
Takeda R, Takagi M, Shinohara H, Futagawa H, Narumi S, Hasegawa T, Nishimura G, Yoshihashi H.
Eur J Med Genet 60 635-638 2017
Research paper (scientific journal), Joint Work, Accepted
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A novel case of somatic KCNJ5 mutation in pediatric-onset aldosterone-producing adenoma.
Uchida N, Amano N, Yamaoka Y, Uematsu A, Sekine Y, Suzuki M, Watanabe J, Nishimoto K, Mukai K, Fukuzawa R, Hasegawa T, Ishii T.
J Endocrine Society 1 1056-1061 2017
Research paper (scientific journal), Joint Work, Accepted
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Genetic defects in pediatric-onset adrenal insufficiency in Japan.
Amano N, Narumi S, Hayashi M, Takagi M, Imai K, Nakamura T, Hachiya R, Sasaki G, Homma K, Ishii T, Hasegawa T.
Eur J Endocrinol 177 187-194 2017
Research paper (scientific journal), Joint Work, Accepted
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The response to growth hormone treatment in prepubertal children with growth hormone deficiency in Japan: Comparing three consecutive years of treatment data of The Foundation for Growth Science in Japan between the 1990s and 2000s.
Isojima T, Hasegawa T, Yokoya S, Tanaka T.
Endor J 30 851-858 2017
Research paper (scientific journal), Joint Work, Accepted
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Homozygous DUOXA2 mutation (p.Tyr138*) in a girl with congenital hypothyroidism and her apparently unaffected brother: Case report and review of the literature.
Sugisawa C, Higuchi S, Takagi M, Hasegawa Y, Taniyama M, Abe K, Hasegawa T, Narumi S.
Endocr J 64 807-812 2017
Research paper (scientific journal), Joint Work, Accepted
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Clinical practice guideline for congenital hyperinsulinism.
Yorifuji T, Horikawa R, Hasegawa T, Adachi M, Soneda S, Minagawa M, Ida S, Yonekura T, Kinoshita Y, Kanamori Y, Kitagawa M, Shinakai M, Sasaki H, Nio M.
Clin Pediatr Endocrinol 26 127-152 2017
Research paper (scientific journal), Joint Work, Accepted