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[HDR syndrome (GATA3 haploinsufficiency syndrome)].
Mochizuki T, Fujita K, Yamada H, Ogata T. Mochizuki T, et al. Among authors: fujita k. Nihon Rinsho. 2006 Jun 28;Suppl 2:74-6. Nihon Rinsho. 2006. PMID: 16817354 Review. Japanese. No abstract available.
Four Japanese patients with adrenal hypoplasia congenita and hypogonadotropic hypogonadism caused by DAX-1 gene mutations: mutant DAX-1 failed to repress steroidogenic acute regulatory protein (StAR) and luteinizing hormone beta-subunit gene promoter activity.
Okuhara K, Abe S, Kondo T, Fujita K, Koda N, Mochizuki H, Fujieda K, Tajima T. Okuhara K, et al. Among authors: fujita k. Endocr J. 2008 Mar;55(1):97-103. doi: 10.1507/endocrj.k07e-008. Epub 2008 Jan 17. Endocr J. 2008. PMID: 18202527 Free article.
Clinical evaluation of recombinant human growth hormone in Noonan syndrome.
Ogawa M, Moriya N, Ikeda H, Tanae A, Tanaka T, Ohyama K, Mori O, Yazawa T, Fujita K, Seino Y, Kubo T, Tanaka H, Nishi Y, Yoshimoto M. Ogawa M, et al. Among authors: fujita k. Endocr J. 2004 Feb;51(1):61-8. doi: 10.1507/endocrj.51.61. Endocr J. 2004. PMID: 15004410 Free article. Clinical Trial.
Clinical characteristics, etiologies and pathophysiology of patients with severe short stature with severe GH deficiency: questionnaire study on the data registered with the foundation for growth science, Japan.
Hanew K, Tachibana K, Yokoya S, Fujieda K, Tanaka T, Igarashi Y, Shimatsu A, Tanaka H, Tanizawa T, Teramoto A, Nishi Y, Hasegawa Y, Hizuka N, Hirano T, Fujita K. Hanew K, et al. Among authors: fujita k. Endocr J. 2006 Apr;53(2):259-65. doi: 10.1507/endocrj.53.259. Endocr J. 2006. PMID: 16618986 Free article.
Studies of very severe short stature with severe GH deficiency: from the data registered with the foundation for growth science.
Hanew K, Tachibana K, Yokoya S, Fujieda K, Tanaka T, Igarashi Y, Shimatsu A, Tanaka H, Tanizawa T, Teramoto A, Nishi Y, Hasegawa Y, Hizuka N, Hirano T, Fujita K; GH Treatment Study Committee, The Foundation for Growth Science, Japan. Hanew K, et al. Among authors: fujita k. Endocr J. 2005 Feb;52(1):37-43. doi: 10.1507/endocrj.52.37. Endocr J. 2005. PMID: 15758556 Free article.
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. Tanaka T, et al. Among authors: fujita k. Clin Pediatr Endocrinol. 2015 Oct;24(4):167-73. doi: 10.1297/cpe.24.167. Epub 2015 Oct 24. Clin Pediatr Endocrinol. 2015. PMID: 26568657 Free PMC article.
5,074 results