Papers - Hasegawa, Tomonobu
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Frequencies of spontaneous breast development and spontaneous menarche in Turner syndrome in Japan.
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.
Clin Pediatr Endocrinol 24 3167 - 3173 2015
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A novel mutation of THRB Gene in a Japanese family with resistance to thyroid hormone.
Ito J, Narumi S, Nishizawa K, Kamimaki T, Hori N, Hasegawa T
Clin Pediatr Endocrinol in press 2015
Joint Work
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Distinguishing from primary from secondary delta4-3-oxisteroid 5-reductase (SRD5B1, AKR1D1) deficiencyby urinary ateroid analysis.
Yanagi T, Mizuochi T, Homma K, Ueki I, Seki Y, Hasegawa T, Takei H, Nittono H, Kurosawa T, Matsuishi T, Kimura A
Clin Endocrinol 82 346 - 351 2015
Joint Work
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Pseudodominant Inheritance in a Family with Non-autoimmune Hypothyroidism due to Biallelic DUOX2 Mutations.
Abe K, Narumi S, Suwanai AS, Hamajima T, Hasegawa T
Clin Endocrinol 83 394 - 398 2015
Joint Work
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Elevated levels of plasma immunoassayable aldosterone in a mild form of 17-hydroxylaase/17,20-lyase deficiency diagnosed at the age of 50.
Ueda K, Usui T, Watanabe T, Kaneko K, Nakatani R, Kakita-Kobayashi M, Tanase-Nakao K, Nanba K, Tsuiki M, Tagami T, Naruse M, Toyoda Y, Homma K, Hasegawa T, Shimatsu A
AACE Clin Case Reports 1 e156 - e160 2015
Joint Work
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Osteogenesis imperfecta IIC caused by a novel heterozygous mutation in the C-prppeptide region of COL1A1.
Takagi M, Matsushita M, Nishimura G, Hasegawa T
Human Genome Variation 1 14025 2015
Joint Work
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Trends in thin body stature among Japanese female adolescents, 2003 to 2012.
Inokuchi M, Matsuo N, Takayama JI, Hasegawa T
Ann Hum Biol. 42 533 - 537 2015
Joint Work
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Heterozygous defects in PAX6 gene and congenital hypopituitarism.
Takagi M, Nagasaki K, Fujiwara I, Ishii T, Amano N, Asakura Y, Muroya K, Hasegawa Y, Adachi M, Hasegawa T
Eur J Endocrinol 172 37 - 45 2015
Joint Work
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Waist Circumference centiles by age and sex for Japanese children based on the 1978-1981 cross-sectional national survey data.
Anzo M, Inokkuchi M, Matsuo N, Takayama JI, Hasegawa T
Ann Hum Biol 42 56 - 61 2015
Joint Work
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Treatment of situation of male hypogonadotropic hypogonadism in pediatrics and proposal of testosterone and gonadotropins replacement therapy protocols.
Sato N, Hasegawa T, Hasegawa Y, Arisaka O, Ozono K, Amemiya S, Kikuchi T, Tanaka H, Harada S, Miyata J, Tanaka T
Clin Pediatr Endocrinol 24 37 - 49 2015
Joint Work
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Adult phenylketonuria presenting with subacute severe neurologic symptoms.
Seki M, Takizawa T, Suzuki S, Shimizu T, Shibata H, Ishii T, Hasegawa T, Suzuki N
J Clin Neuroscience 22 1361 - 1363 2015
Joint Work
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A case with neonatal hyperinsulinemic hypoglycemia: It is a characteristic complication of Sotos syndrome.
Nakamura Y, Takagi M, Yoshihashi H, Miura M, Narumi S, Hasegawa T, Miyake Y, Hasegawa Y
Am J Med Genet 167A 1627 - 1631 2015
Joint Work
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Severe osteogenesis imperfect caused by double substitutions of triple helical glycine residues in COL1A2.
Takagi M, Shinohara H, Narumi S, Nishimura G, Hasegawa Y, Hasegawa T
Am J Med Genet A 167 1627 - 1631 2015
Joint Work
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A CYP3A4 inhibitor counterscts the mitotane-induced adrenal insufficiency and resistant hypertention in adrenocortical carcinoma.
Minami I, Yoshimoto T, Tsujimoto K, Homma K, Hasegawa T, Ogawa Y
AACE Clin Case Reports in press 2015
Joint Work
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A novel mutation Ser344Cys in FGFR3 causes achondroplasia with severe platyspondyly.
Takagi M, Kouwaki M, Kawase K, Shinohara H, Hasegawa Y, Yamada T, Fujiwara I, Sawai H, Nishimura G, Hasegawa T
Am J Med Genet 167A 2851 - 2854 2015
Joint Work
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Polyostotic osteolysis and hypophosphatemic rickets with elevated serum fibroblast growth factor 23: a case report.
Sato T, Muroya K, Asakura Y, Yachie A, Nishimura G, Aida N, Machida J, Tanaka Y, Hasegawa T, Adachi M
Am J Med Genet 167A 2430 - 2434 2015
Joint Work
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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.
Sato T, Muroya K, Hanakawa J, Asakura Y, Tanaka Y, Murayama K, Ohtake A, Hasegawa T, Adachi M
Eur J Pediatr 174 1593 - 1602 2015
Joint Work
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Human chorionic gonadotropin stimulation test in prepubertal children with micropenis can accurately predict Leydig cell function in pubertal or postpubertal adolescents.
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
Hor Res Paediatr 84 305 - 310 2015
Joint Work
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Combined GH and TSH deficiency in a Japanese patient with a novel frameshift mutation in IGSF1.
Asakura Y, Abe K, Muroya K, Hanakawa J, Oto Y, Narumi S, Hasegawa T, Adachi M
Hor Res Pediatr 84 349 - 354 2015
Joint Work
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小児における内分泌機能検査の注意点
志村和浩、長谷川奉延。
ホルモンと臨床 (医学の世界社) 62 ( 4 ) 341 - 343 2014.04
Joint Work