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Problems in diagnosing atypical Gitelman's syndrome presenting with normomagnesaemia.
Nakamura A, Shimizu C, Nagai S, Yoshida M, Aoki K, Kondo T, Miyoshi H, Wada N, Tajima T, Terauchi Y, Yoshioka N, Koike T. Nakamura A, et al. Among authors: kondo t. Clin Endocrinol (Oxf). 2010 Feb;72(2):272-6. doi: 10.1111/j.1365-2265.2009.03649.x. Epub 2009 Jun 8. Clin Endocrinol (Oxf). 2010. PMID: 19508680
Perilipin overexpression in white adipose tissue induces a brown fat-like phenotype.
Sawada T, Miyoshi H, Shimada K, Suzuki A, Okamatsu-Ogura Y, Perfield JW 2nd, Kondo T, Nagai S, Shimizu C, Yoshioka N, Greenberg AS, Kimura K, Koike T. Sawada T, et al. Among authors: kondo t. PLoS One. 2010 Nov 16;5(11):e14006. doi: 10.1371/journal.pone.0014006. PLoS One. 2010. PMID: 21103377 Free PMC article.
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: kondo t. 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.
[Adverse effects of sulfonylurea drugs].
Kondo T, Yoshioka N, Koike T. Kondo T, et al. Nihon Rinsho. 2007 Oct 28;65 Suppl 8:178-81. Nihon Rinsho. 2007. PMID: 18074535 Review. Japanese. No abstract available.
7,618 results