論文 - 長谷川　奉延

Growth references for Japanese individuals with Noonan syndrome.

Isojima T, Sakatsume S, Hasegawa T, Ogata T, Nakanishi T, Nagai T, Yokoya S.

Pediatr Res  79   543-548 2016年

研究論文（学術雑誌）, 共著, 査読有り

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  25   19-22 2016年

研究論文（学術雑誌）, 共著, 査読有り

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 （ 4 ） 3167 - 3173 2015年10月

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年

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年

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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年

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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年

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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年

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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年

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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年

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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年

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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年

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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年

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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年

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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年

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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年

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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年

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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年

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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年

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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年

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