Nagasaka H - Search Results

1

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. Metabolism. 2009 Jan;58(1):48-54. doi: 10.1016/j.metabol.2008.08.005. Metabolism. 2009. PMID: 19059530

2

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. J Pediatr Gastroenterol Nutr. 2007 Jul;45(1):96-105. doi: 10.1097/MPG.0b013e3180331df9. J Pediatr Gastroenterol Nutr. 2007. PMID: 17592371

3

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. 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

4

Evaluation of endogenous nitric oxide synthesis in congenital urea cycle enzyme defects.

Nagasaka H, Tsukahara H, Yorifuji T, Miida T, Murayama K, Tsuruoka T, Takatani T, Kanazawa M, Kobayashi K, Okano Y, Takayanagi M. Nagasaka H, et al. Metabolism. 2009 Mar;58(3):278-82. doi: 10.1016/j.metabol.2008.09.025. Metabolism. 2009. PMID: 19217439

5

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. 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

6

Altered metabolisms of mediators controlling vascular function and enhanced oxidative stress in asymptomatic children with congenital portosystemic venous shunt.

Nagasaka H, Okano Y, Aizawa M, Miida T, Yorifuji T, Tajima G, Sakura N, Takatani T, Sanayama Y, Sugamoto K, Mayumi M, Kobayashi K, Hirano K, Takayanagi M, Tsukahara H. Nagasaka H, et al. Metabolism. 2010 Jan;59(1):107-13. doi: 10.1016/j.metabol.2009.07.013. Epub 2009 Sep 18. Metabolism. 2010. PMID: 19766269

7

Favorable effect of 4-phenylacetate on liver functions attributable to enhanced bile salt export pump expression in ornithine transcarbamylase-deficient children.

Nagasaka H, Yorifuji T, Kobayashi K, Takikawa H, Komatsu H, Inui A, Fujisawa T, Miida T, Tsukahara H, Takatani T, Hayashi H. Nagasaka H, et al. Mol Genet Metab. 2010 Jun;100(2):123-8. doi: 10.1016/j.ymgme.2010.02.008. Epub 2010 Feb 16. Mol Genet Metab. 2010. PMID: 20219403

8

CD36 deficiency predisposing young children to fasting hypoglycemia.

Nagasaka H, Yorifuji T, Takatani T, Okano Y, Tsukahara H, Yanai H, Hirano K, Hui SP, Hirayama S, Ito T, Chiba H, Miida T. Nagasaka H, et al. Metabolism. 2011 Jun;60(6):881-7. doi: 10.1016/j.metabol.2010.08.008. Epub 2010 Oct 13. Metabolism. 2011. PMID: 20947105

9

Evaluation of risk for atherosclerosis in Alagille syndrome and progressive familial intrahepatic cholestasis: two congenital cholestatic diseases with different lipoprotein metabolisms.

Nagasaka H, Yorifuji T, Egawa H, Yanai H, Fujisawa T, Kosugiyama K, Matsui A, Hasegawa M, Okada T, Takayanagi M, Chiba H, Kobayashi K. Nagasaka H, et al. J Pediatr. 2005 Mar;146(3):329-35. doi: 10.1016/j.jpeds.2004.10.047. J Pediatr. 2005. PMID: 15756213

10

Effects of arginine treatment on nutrition, growth and urea cycle function in seven Japanese boys with late-onset ornithine transcarbamylase deficiency.

Nagasaka H, Yorifuji T, Murayama K, Kubota M, Kurokawa K, Murakami T, Kanazawa M, Takatani T, Ogawa A, Ogawa E, Yamamoto S, Adachi M, Kobayashi K, Takayanagi M. Nagasaka H, et al. Eur J Pediatr. 2006 Sep;165(9):618-24. doi: 10.1007/s00431-006-0143-y. Epub 2006 May 16. Eur J Pediatr. 2006. PMID: 16703326 Clinical Trial.

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