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Page 1
Cross-sectional study of bone metabolism with nutrition in adult classical phenylketonuric patients diagnosed by neonatal screening.
Nagasaka H, Tsukahara H, Takatani T, Sanayama Y, Takayanagi M, Ohura T, Sakamoto O, Ito T, Wada M, Yoshino M, Ohtake A, Yorifuji T, Hirayama S, Miida T, Fujimoto H, Mochizuki H, Hattori T, Okano Y. Nagasaka H, et al. Among authors: ohtake a. J Bone Miner Metab. 2011 Nov;29(6):737-43. doi: 10.1007/s00774-011-0276-6. Epub 2011 May 19. J Bone Miner Metab. 2011. PMID: 21594581
Oxysterol changes along with cholesterol and vitamin D changes in adult phenylketonuric patients diagnosed by newborn mass-screening.
Nagasaka H, Okano Y, Kimura A, Mizuochi T, Sanayama Y, Takatani T, Nakagawa S, Hasegawa E, Hirano K, Mochizuki H, Ohura T, Ishige-Wada M, Usui H, Yorifuji T, Tsukahara H, Hirayama S, Ohtake A, Yamato S, Miida T. Nagasaka H, et al. Among authors: ohtake a. Clin Chim Acta. 2013 Feb 1;416:54-9. doi: 10.1016/j.cca.2012.10.011. Epub 2012 Nov 17. Clin Chim Acta. 2013. PMID: 23168022
Experimental evidence that phenylalanine is strongly associated to oxidative stress in adolescents and adults with phenylketonuria.
Sanayama Y, Nagasaka H, Takayanagi M, Ohura T, Sakamoto O, Ito T, Ishige-Wada M, Usui H, Yoshino M, Ohtake A, Yorifuji T, Tsukahara H, Hirayama S, Miida T, Fukui M, Okano Y. Sanayama Y, et al. Among authors: ohtake a. Mol Genet Metab. 2011 Jul;103(3):220-5. doi: 10.1016/j.ymgme.2011.03.019. Epub 2011 Mar 29. Mol Genet Metab. 2011. PMID: 21514861
Sustained high plasma mannose less sensitive to fluctuating blood glucose in glycogen storage disease type Ia children.
Nagasaka H, Yorifuji T, Bandsma RH, Takatani T, Asano H, Mochizuki H, Takuwa M, Tsukahara H, Inui A, Tsunoda T, Komatsu H, Hiejima E, Fujisawa T, Hirano K, Miida T, Ohtake A, Taguchi T, Miwa I. Nagasaka H, et al. Among authors: ohtake a. J Inherit Metab Dis. 2013 Jan;36(1):75-81. doi: 10.1007/s10545-012-9514-x. Epub 2012 Sep 13. J Inherit Metab Dis. 2013. PMID: 22971957
Fluctuating liver functions in siblings with MPV17 mutations and possible improvement associated with dietary and pharmaceutical treatments targeting respiratory chain complex II.
Kaji S, Murayama K, Nagata I, Nagasaka H, Takayanagi M, Ohtake A, Iwasa H, Nishiyama M, Okazaki Y, Harashima H, Eitoku T, Yamamoto M, Matsushita H, Kitamoto K, Sakata S, Katayama T, Sugimoto S, Fujimoto Y, Murakami J, Kanzaki S, Shiraki K. Kaji S, et al. Among authors: ohtake a. Mol Genet Metab. 2009 Aug;97(4):292-6. doi: 10.1016/j.ymgme.2009.04.014. Epub 2009 May 12. Mol Genet Metab. 2009. PMID: 19520594
Indian childhood cirrhosis-like disease in a Japanese boy undergoing liver transplantation.
Nagasaka H, Kobayashi K, Yorifuji T, Kage M, Kimura A, Takayanagi M, Kikuta H, Egawa H, Tanaka K, Inui A, Fujisawa T, Ohtake A. Nagasaka H, et al. Among authors: ohtake a. J Pediatr Gastroenterol Nutr. 1999 Nov;29(5):598-600. doi: 10.1097/00005176-199911000-00024. J Pediatr Gastroenterol Nutr. 1999. PMID: 10554131 No abstract available.
276 results