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Genotyping of congenital adrenal hyperplasia due to 21-hydroxylase deficiency presenting as male infertility: case report and literature review.
Sugino Y, Usui T, Okubo K, Nagahama K, Takahashi T, Okuno H, Hatayama H, Ogawa O, Shimatsu A, Nishiyama H. Sugino Y, et al. Among authors: shimatsu a. J Assist Reprod Genet. 2006 Sep-Oct;23(9-10):377-80. doi: 10.1007/s10815-006-9062-0. Epub 2006 Oct 11. J Assist Reprod Genet. 2006. PMID: 17033937 Free PMC article.
Histopathological diagnosis of primary aldosteronism using CYP11B2 immunohistochemistry.
Nanba K, Tsuiki M, Sawai K, Mukai K, Nishimoto K, Usui T, Tagami T, Okuno H, Yamamoto T, Shimatsu A, Katabami T, Okumura A, Kawa G, Tanabe A, Naruse M. Nanba K, et al. Among authors: shimatsu a. J Clin Endocrinol Metab. 2013 Apr;98(4):1567-74. doi: 10.1210/jc.2012-3726. Epub 2013 Feb 26. J Clin Endocrinol Metab. 2013. PMID: 23443813
Confirmatory testing in primary aldosteronism.
Nanba K, Tamanaha T, Nakao K, Kawashima ST, Usui T, Tagami T, Okuno H, Shimatsu A, Suzuki T, Naruse M. Nanba K, et al. Among authors: shimatsu a. J Clin Endocrinol Metab. 2012 May;97(5):1688-94. doi: 10.1210/jc.2011-2504. Epub 2012 Mar 14. J Clin Endocrinol Metab. 2012. PMID: 22419718
¹⁸F-FDG-PET-positive adrenal tumour.
Kakita-Kobayashi M, Usui T, Sasano H, Shimatsu A. Kakita-Kobayashi M, et al. Among authors: shimatsu a. BMJ Case Rep. 2015 Mar 6;2015:bcr2015209379. doi: 10.1136/bcr-2015-209379. BMJ Case Rep. 2015. PMID: 25750227 Free PMC article. No abstract available.
360 results