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Molecular and clinical analysis of Japanese patients with persistent congenital hyperinsulinism: predominance of paternally inherited monoallelic mutations in the KATP channel genes.
Yorifuji T, Kawakita R, Nagai S, Sugimine A, Doi H, Nomura A, Masue M, Nishibori H, Yoshizawa A, Okamoto S, Doi R, Uemoto S, Nagasaka H. Yorifuji T, et al. Among authors: uemoto s. J Clin Endocrinol Metab. 2011 Jan;96(1):E141-5. doi: 10.1210/jc.2010-1281. Epub 2010 Oct 13. J Clin Endocrinol Metab. 2011. PMID: 20943781
Effects of bezafibrate on dyslipidemia with cholestasis in children with familial intrahepatic cholestasis-1 deficiency manifesting progressive familial intrahepatic cholestasis.
Nagasaka H, Yorifuji T, Hirano K, Ota A, Toyama-Nakagawa Y, Takatani T, Tsukahara H, Kobayashi K, Takayanagi M, Inomata Y, Uemoto S, Miida T. Nagasaka H, et al. Among authors: uemoto s. Metabolism. 2009 Jan;58(1):48-54. doi: 10.1016/j.metabol.2008.08.005. Metabolism. 2009. PMID: 19059530
[Surgical treatment of carcinoma of the pancreas].
Doi R, Kami K, Ito D, Kawaguchi Y, Uemoto S, Yoshida S. Doi R, et al. Among authors: uemoto s. Nihon Geka Gakkai Zasshi. 2006 Jul;107(4):168-72. Nihon Geka Gakkai Zasshi. 2006. PMID: 16878408 Review. Japanese.
Relationship between oxidative stress and antioxidant systems in the liver of patients with Wilson disease: hepatic manifestation in Wilson disease as a consequence of augmented oxidative stress.
Nagasaka H, Inoue I, Inui A, Komatsu H, Sogo T, Murayama K, Murakami T, Yorifuji T, Asayama K, Katayama S, Uemoto S, Kobayashi K, Takayanagi M, Fujisawa T, Tsukahara H. Nagasaka H, et al. Among authors: uemoto s. Pediatr Res. 2006 Oct;60(4):472-7. doi: 10.1203/01.pdr.0000238341.12229.d3. Epub 2006 Aug 28. Pediatr Res. 2006. PMID: 16940238
1,077 results