Published papers
Hasegawa, Tomonobu
121-140 items (total 510)
Steroidogenic pathways involved in androgen biosynthesis in eumenorrheic women and patients with polycystic ovary syndrome.
- Author
- Saito K, Matsuzaki T, Iwasa T, Miyado M, Saito H, Hasegawa T, Homma K, Inoue E, Miyashiro Y, Kubota T, Irahara M, Ogata T, Fukami M.
- Publication Title
- Magazine name J Steroid Biochem Mol Biol Start Page 31-37 (Publication Date）2016）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
Women with Turner syndrome are at high risk of lifestyle-related disease –From questionnaire surveys by the Foundation for Growth Science in Japan.
- Author
- Hanew K, Tanaka T, Horikawa R, Hasegawa T, Fujita K, Yokoya S.
- Publication Title
- Magazine name Endocrine J Start Page 449-456 (Publication Date）2016）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
Stippled calcification in an infant with a recurrent SRCAP gene mutation.
- Author
- Yagi H, Takagi M, Narumi S, Hasegawa T, Nishimura G, Hasegawa Y.
- Publication Title
- Magazine name Am J Med Gent A Start Page 1088-1091 (Publication Date）2016）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
Potential utility of cinacalcet as a treatment for CDC73-1 related primary hyperparathyroidism: a case report.
- Author
- Sato T, Muroya K, Hanakawa J, Yamashita S, Nozawa K, Masudo K, Yamanaka T, Asakura Y, Hasegawa T. Adachi M.
- Publication Title
- Magazine name Clin Pediatr Endocrinol Start Page 91-98 (Publication Date）2016）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7.
- Author
- Narumi S, Amano N, Ishii T, Katsumata N, Muroya K, Adachi M, Toyoshima K, Tanaka Y, Fukuzawa R, Miyako K, Kinjo S, Ohga S, Ihara K, Inoue H, Kinjo T, Hara T, Kohno M, Yamada S,Urano H, Kitagawa Y, Tsugawa K, Higa A, Miyawaki M, Okutani T, Kizaki Z, Hamada H, Kihara M, Shiga K, Yamaguchi T, Kenmochi M, Kitajima H, Fukami M, Shimizu A, Kudoh J, Shibata S, Okano H, Miyake N, Mastumoto N, Hasegawa T.
- Publication Title
- Magazine name Nat Genet Start Page 792-797 (Publication Date）2016）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
Gonadal macrophage infiltration in congenital lipoid adrenal hyperplasia.
- Author
- Ishii T, Fukuzawa R, Sato T, Muroya K, Adachi M, Ihara K, Igaki J, Hasegawa Y, Sato S, Mitsui T, Hasegawa T.
- Publication Title
- Magazine name Eur J Endocrinol Start Page 127-132 (Publication Date）2016）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
A Novel dominant negative mutation in the intracellular domain of GHR is associated with growth hormone insensitivity.
- Author
- Takagi M, Shinohara H, Nagashima Y, Hasegawa Y, Narumi S, Hasegawa T.
- Publication Title
- Magazine name Clin Endocrinol Start Page 669-671 (Publication Date）2016）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
A patient with pseudohypoaldosteronism type II complicated by congenital hypopituitarism carrying a KLHL3 mutation.
- Author
- Mitani M, Furuichi M, Narumi S, Hasegawa T, Chiga M, Uchida S, Sato S.
- Publication Title
- Magazine name Clin Pediat Endocrinol Start Page 127-134 (Publication Date）2016）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
Long-term clinical course in three patients with MAMLD1 mutations.
- Author
- Fujisawa Y, Fukami M, Hasegawa T, Uematsu A, Koji M, Ogata T, Muroya K,
- Publication Title
- Magazine name Endocrine J Start Page 835-839 (Publication Date）2016）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
Novel heterozygous mutation in the extracellular domain of FGFR1 associated with Hartsfield Syndrome.
- Author
- Takagi M, Miyoshi T, Nagashima Y, Shibata N, Yagi H, Fukuzawa R , Hasegawa T.
- Publication Title
- Magazine name Hum Genome Var Start Page 16034 (Publication Date）2016）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
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）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
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）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
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）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
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）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
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）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
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）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
Steroidogenic pathways involved in androgen biosynthesis in eumenorrheic women and patients with polycystic ovary syndrome.
- Author
- Saito K, Matsuzaki T, Iwasa T, Miyado M, Saito H, Hasegawa T, Homma K, Inoue E, Miyashiro Y, Kubota T, Irahara M, Ogata T, Fukami M.
- Publication Title
- Magazine name J Steroid Biochem Mol Biol Start Page 31-37 (Publication Date）2016）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
Women with Turner syndrome are at high risk of lifestyle-related disease –From questionnaire surveys by the Foundation for Growth Science in Japan.
- Author
- Hanew K, Tanaka T, Horikawa R, Hasegawa T, Fujita K, Yokoya S.
- Publication Title
- Magazine name Endocrine J Start Page 449-456 (Publication Date）2016）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
Stippled calcification in an infant with a recurrent SRCAP gene mutation.
- Author
- Yagi H, Takagi M, Narumi S, Hasegawa T, Nishimura G, Hasegawa Y.
- Publication Title
- Magazine name Am J Med Gent A Start Page 1088-1091 (Publication Date）2016）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
Potential utility of cinacalcet as a treatment for CDC73-1 related primary hyperparathyroidism: a case report.
- Author
- Sato T, Muroya K, Hanakawa J, Yamashita S, Nozawa K, Masudo K, Yamanaka T, Asakura Y, Hasegawa T. Adachi M.
- Publication Title
- Magazine name Clin Pediatr Endocrinol Start Page 91-98 (Publication Date）2016）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With