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Page 1
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: miida t. 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
Depletion of high-density lipoprotein and appearance of triglyceride-rich low-density lipoprotein in a Japanese patient with FIC1 deficiency manifesting benign recurrent intrahepatic cholestasis.
Nagasaka H, Chiba H, Hui SP, Takikawa H, Miida T, Takayanagi M, Yorifuji T, Hasegawa M, Ota A, Hirano K, Kikuchi H, Tsukahara H, Kobayashi K. Nagasaka H, et al. Among authors: miida t. J Pediatr Gastroenterol Nutr. 2007 Jul;45(1):96-105. doi: 10.1097/MPG.0b013e3180331df9. J Pediatr Gastroenterol Nutr. 2007. PMID: 17592371
Reduced apolipoprotein E-rich high-density lipoprotein level at birth is restored to the normal range in patients with familial hypercholesterolemia in the first year of life.
Nagasaka H, Miida T, Hirano K, Ota A, Yorifuji T, Takatani T, Tsukahara H, Takayanagi M, Hui SP, Kobayashi K, Chiba H. Nagasaka H, et al. Among authors: miida t. J Clin Endocrinol Metab. 2008 Mar;93(3):779-83. doi: 10.1210/jc.2007-1621. Epub 2008 Jan 8. J Clin Endocrinol Metab. 2008. PMID: 18182454
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: miida t. Metabolism. 2009 Jan;58(1):48-54. doi: 10.1016/j.metabol.2008.08.005. Metabolism. 2009. PMID: 19059530
Sustaining hypercitrullinemia, hypercholesterolemia and augmented oxidative stress in Japanese children with aspartate/glutamate carrier isoform 2-citrin-deficiency even during the silent period.
Nagasaka H, Okano Y, Tsukahara H, Shigematsu Y, Momoi T, Yorifuji J, Miida T, Ohura T, Kobayashi K, Saheki T, Hirano K, Takayanagi M, Yorifuji T. Nagasaka H, et al. Among authors: miida t. Mol Genet Metab. 2009 May;97(1):21-6. doi: 10.1016/j.ymgme.2009.01.009. Epub 2009 Jan 25. Mol Genet Metab. 2009. PMID: 19232506
Lipoprotein profiles in children with two common cholesteryl ester transfer protein gene mutations, D442G and I14A, during the first year of life.
Nagasaka H, Yorifuji T, Momoi T, Yorifuji J, Hirano K, Ota A, Takatani T, Tsukahara H, Takayanagi M, Kobayashi K, Chiba H, Sato Y, Miida T. Nagasaka H, et al. Among authors: miida t. Clin Chim Acta. 2009 Aug;406(1-2):52-6. doi: 10.1016/j.cca.2009.05.007. Epub 2009 May 19. Clin Chim Acta. 2009. PMID: 19463799
276 results