Published papers
Hasegawa, Tomonobu
81-100 items (total 510)
The distribution and cellular lineages of XX and XY cells in gonads associated with ovotesticular disorder of sexual development.
- Author
- Nishina-Uchida N, Fukuzawa R, Ishii T, Anaka MR, Hasegawa T, Hasegawa Y.
- Publication Title
- Magazine name Sex Dev. Start Page 185-190 (Publication Date）2016）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
A case of transient neonatal diabetes due to a novel mutation in ABCC8.
- Author
- Takagi M, Takeda R, Yagi H, Ariyasu D, Fukuzawa R, Hasegawa T.
- Publication Title
- Magazine name Clin Pediatr Endocrinol Start Page 139-141 (Publication Date）2016）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
Effects of financial support on treatment of adolescents with growth hormone deficiency: a retrospective study in Japan.
- Author
- Maeda E, Higashi T, Hasegawa T, Yokoya S, Mochizuki T, Ishii T, Ito J, Kanzaki S, Shimatsu A, Takano K, Tajim T, Tanaka H, Tanahashi Y, Teramoto A, Nagai T, Hanew K, Horikawa R, Yorifuji T, Wada N, Tanaka T.
- Publication Title
- Magazine name BMC Health Services Research Start Page 602 (Publication Date）2016）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
Feminizing adrenocortical cartinoma with distinct histopathological findings.
- Author
- Hatano M, Takenaka Y, Inoue I, Homma K, Hasegawa T, Sasano H, Awata T, Katayama S.
- Publication Title
- Magazine name Intern Med Start Page 3301-3307 (Publication Date）2016）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
A novel heterozygous intronic mutation in POU1F1 is associated with combined pituitary hormone deficiency.
- Author
- Takagi M, Kamasaki H, Yagi H, Fukuzawa R, Narumi S, Hasegawa T.
- Publication Title
- Magazine name Endocrine J Start Page 229-234 (Publication Date）2017）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
A novel de novo germline mutation Glu40Lys in AKT3 causes megalencephaly with growth hormone deficiency.
- Author
- Takagi M, Dobashi K, Nagahara K, Kato M, Nishimura G, Fukuzawa R, Narumi S, Hasegawa T.
- Publication Title
- Magazine name Am J Med Genet A Start Page 1071-1076 (Publication Date）2017）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
A novel mutation in the C-propeptide of COL2A1 causes atypical spondyloepiphyseal dysplasia cogenita.
- Author
- Kusano C, Takagi M, Hori N, Murotsuki J, Nishimura G, Hasegawa T.
- Publication Title
- Magazine name Hum Genome Var Start Page 17003 (Publication Date）2017）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
Histological Change of Autoimmune Hepatitis with Graves’ disease; a child case report.
- Author
- Yamada M, Shibata H, Masugi Y, Ishii T, Kameyama K, Ebinuma H, Hasegawa T.
- Publication Title
- Magazine name Inter Med Start Page 2139-2143 (Publication Date）2017）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
FGFR1 Analyses in Four Patients with Hypogonadotropic Hypogonadism with Split-Hand/Foot Malformation: Implications for the Promoter Region.
- Author
- Ohtaka K, Fujisawa Y, Takada F, Seo M, Kameda H, Hasegawa Y, Hasegawa T, Fukami M, Ogata T.
- Publication Title
- Magazine name Hum Mutation Start Page 503-506 (Publication Date）2017）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
Shimada H. Severe hypertriglyceridemia during treatment of acute lymphoblastic leukemia associated with type III hyperlipoproteinemia
- Author
- Yamada Y, Shima H, Shibata H, Ishii T, Hasegawa T,
- Publication Title
- Magazine name Pediatr Blood Cancer Volume 64(Issue 11) (Publication Date）2017）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
yndromic disorder of sex development due to a novel hemizygous mutation in the carboxyl-terminal domain of ATRX.
- Author
- Takagi M, Yagi H, Fukuzawa R, Narumi S, Hasegawa T.
- Publication Title
- Magazine name Hum Genome Var Start Page 17012 (Publication Date）2017）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
Three-quarters adrenalectomy for infantile-onset Cushing syndrome due to bilateral adrenal hyperplasia in McCune-Albright syndrome.
- Author
- Itonaga T, Goto H, Toujigamori M, Ohno Y, Korematsu S, TIzumi T, Narumi S, Hasegawa T, Ihara K.
- Publication Title
- Magazine name Hor Res Paediatr Start Page 285-290 (Publication Date）2017）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
Validation of auxological reference values for Japanese children with Noonan syndrome and comparison with growth in children with Turner syndrome.
- Author
- Isojima T, Sakazume S, Hasegawa T, Ogata T, Nakanishi T, Nagai T, Yokoya S.
- Publication Title
- Magazine name Clin Pediatr Endocrinol Start Page 153-164 (Publication Date）2017）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
Clinical practice guideline for congenital hyperinsulinism.
- Author
- 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.
- Publication Title
- Magazine name Clin Pediatr Endocrinol Start Page 127-152 (Publication Date）2017）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
Homozygous DUOXA2 mutation (p.Tyr138*) in a girl with congenital hypothyroidism and her apparently unaffected brother: Case report and review of the literature.
- Author
- Sugisawa C, Higuchi S, Takagi M, Hasegawa Y, Taniyama M, Abe K, Hasegawa T, Narumi S.
- Publication Title
- Magazine name Endocr J Start Page 807-812 (Publication Date）2017）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
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.
- Author
- Isojima T, Hasegawa T, Yokoya S, Tanaka T.
- Publication Title
- Magazine name Endor J Start Page 851-858 (Publication Date）2017）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
Genetic defects in pediatric-onset adrenal insufficiency in Japan.
- Author
- Amano N, Narumi S, Hayashi M, Takagi M, Imai K, Nakamura T, Hachiya R, Sasaki G, Homma K, Ishii T, Hasegawa T.
- Publication Title
- Magazine name Eur J Endocrinol Start Page 187-194 (Publication Date）2017）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
A novel case of somatic KCNJ5 mutation in pediatric-onset aldosterone-producing adenoma.
- Author
- Uchida N, Amano N, Yamaoka Y, Uematsu A, Sekine Y, Suzuki M, Watanabe J, Nishimoto K, Mukai K, Fukuzawa R, Hasegawa T, Ishii T.
- Publication Title
- Magazine name J Endocrine Society Start Page 1056-1061 (Publication Date）2017）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
Novel compound heterozygous mutations identified by whole exome sequencing in a Japanese patient with geroderma osteodysplastica.
- Author
- Takeda R, Takagi M, Shinohara H, Futagawa H, Narumi S, Hasegawa T, Nishimura G, Yoshihashi H.
- Publication Title
- Magazine name Eur J Med Genet Start Page 635-638 (Publication Date）2017）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
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)
- Author
- 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.
- Publication Title
- Magazine name Clin Pediatr Endocrinol Start Page 229-241 (Publication Date）2017）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With