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Next generation sequencing-based mutation screening of 86 patients with idiopathic short stature.
Hattori A, Katoh-Fukui Y, Nakamura A, Matsubara K, Kamimaki T, Tanaka H, Dateki S, Adachi M, Muroya K, Yoshida S, Ida S, Mitani M, Nagasaki K, Ogata T, Suzuki E, Hata K, Nakabayashi K, Matsubara Y, Narumi S, Tanaka T, Fukami M. Hattori A, et al. Among authors: tanaka t, tanaka h. Endocr J. 2017 Oct 28;64(10):947-954. doi: 10.1507/endocrj.EJ17-0150. Epub 2017 Aug 3. Endocr J. 2017. PMID: 28768959 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: tanaka t, tanaka h. Endocr J. 2004 Feb;51(1):61-8. doi: 10.1507/endocrj.51.61. Endocr J. 2004. PMID: 15004410 Free article. Clinical Trial.
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: tanaka t, tanaka h. Endocr J. 2005 Feb;52(1):37-43. doi: 10.1507/endocrj.52.37. Endocr J. 2005. PMID: 15758556 Free article.
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: tanaka t, tanaka h. Endocr J. 2006 Apr;53(2):259-65. doi: 10.1507/endocrj.53.259. Endocr J. 2006. PMID: 16618986 Free article.
An observational study of the effectiveness and safety of growth hormone (Humatrope(®)) treatment in Japanese children with growth hormone deficiency or Turner syndrome.
Tai S, Tanaka T, Hasegawa T, Ozono K, Tanaka H, Kanzaki S, Yokoya S, Fujieda K, Chihara K, Seino Y. Tai S, et al. Among authors: tanaka t, tanaka h. Endocr J. 2013;60(1):57-64. doi: 10.1507/endocrj.ej11-0386. Epub 2012 Oct 20. Endocr J. 2013. PMID: 23001148 Free article. Clinical Trial.
Systematic molecular analyses of SHOX in Japanese patients with idiopathic short stature and Leri-Weill dyschondrosteosis.
Shima H, Tanaka T, Kamimaki T, Dateki S, Muroya K, Horikawa R, Kanno J, Adachi M, Naiki Y, Tanaka H, Mabe H, Yagasaki H, Kure S, Matsubara Y, Tajima T, Kashimada K, Ishii T, Asakura Y, Fujiwara I, Soneda S, Nagasaki K, Hamajima T, Kanzaki S, Jinno T, Ogata T, Fukami M; Japanese SHOX study group. Shima H, et al. Among authors: tanaka t, tanaka h. J Hum Genet. 2016 Jul;61(7):585-91. doi: 10.1038/jhg.2016.18. Epub 2016 Mar 17. J Hum Genet. 2016. PMID: 26984564
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