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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: katsumata n. J Clin Endocrinol Metab. 2004 Mar;89(3):1079-88. doi: 10.1210/jc.2003-030476. J Clin Endocrinol Metab. 2004. PMID: 15001591
Hypospadias in a male patient with 21-hydroxylase deficiency.
Kojima-Ishii K, Fujiwara I, Katsumata N, Kanno J, Ogawa E, Tsuchiya S. Kojima-Ishii K, et al. Among authors: katsumata n. Endocr J. 2008 Dec;55(6):1051-4. doi: 10.1507/endocrj.k07e-175. Epub 2008 Aug 22. Endocr J. 2008. PMID: 18719294 Free article.
Prognosis of primary aldosteronism in Japan: results from a nationwide epidemiological study.
Miyake Y, Tanaka K, Nishikawa T, Naruse M, Takayanagi R, Sasano H, Takeda Y, Shibata H, Sone M, Satoh F, Yamada M, Ueshiba H, Katabami T, Iwasaki Y, Tanaka H, Tanahashi Y, Suzuki S, Hasegawa T, Katsumata N, Tajima T, Yanase T. Miyake Y, et al. Among authors: katsumata n. Endocr J. 2014;61(1):35-40. doi: 10.1507/endocrj.ej13-0353. Epub 2013 Sep 28. Endocr J. 2014. PMID: 24077222 Free article.
364 results