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[Kallmann syndrome].
Sato N, Ogata T. Sato N, et al. Among authors: ogata t. Nihon Rinsho. 2006 Jun 28;Suppl 2:220-4. Nihon Rinsho. 2006. PMID: 16817388 Review. Japanese. No abstract available.
Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients.
Sato N, Katsumata N, Kagami M, Hasegawa T, Hori N, Kawakita S, Minowada S, Shimotsuka A, Shishiba Y, Yokozawa M, Yasuda T, Nagasaki K, Hasegawa D, Hasegawa Y, Tachibana K, Naiki Y, Horikawa R, Tanaka T, Ogata T. Sato N, et al. Among authors: ogata t. J Clin Endocrinol Metab. 2004 Mar;89(3):1079-88. doi: 10.1210/jc.2003-030476. J Clin Endocrinol Metab. 2004. PMID: 15001591
Cytochrome P450 oxidoreductase gene mutations and Antley-Bixler syndrome with abnormal genitalia and/or impaired steroidogenesis: molecular and clinical studies in 10 patients.
Fukami M, Horikawa R, Nagai T, Tanaka T, Naiki Y, Sato N, Okuyama T, Nakai H, Soneda S, Tachibana K, Matsuo N, Sato S, Homma K, Nishimura G, Hasegawa T, Ogata T. Fukami M, et al. Among authors: ogata t. J Clin Endocrinol Metab. 2005 Jan;90(1):414-26. doi: 10.1210/jc.2004-0810. Epub 2004 Oct 13. J Clin Endocrinol Metab. 2005. PMID: 15483095
[SHOX haploinsufficiency].
Ogata T. Ogata T. Nihon Rinsho. 2006 May 28;Suppl 1:105-10. Nihon Rinsho. 2006. PMID: 16776105 Review. Japanese. No abstract available.
[Silver-Russell syndrome].
Ogata T. Ogata T. Nihon Rinsho. 2006 May 28;Suppl 1:111-4. Nihon Rinsho. 2006. PMID: 16776106 Review. Japanese. No abstract available.
[HDR syndrome (GATA3 haploinsufficiency syndrome)].
Mochizuki T, Fujita K, Yamada H, Ogata T. Mochizuki T, et al. Among authors: ogata t. Nihon Rinsho. 2006 Jun 28;Suppl 2:74-6. Nihon Rinsho. 2006. PMID: 16817354 Review. Japanese. No abstract available.
2,052 results