Takayanagi M - Search Results

1

Impact of enzyme activity assay on indication in liver transplantation for ornithine transcarbamylase deficiency.

Wakiya T, Sanada Y, Urahashi T, Ihara Y, Yamada N, Okada N, Ushijima K, Otomo S, Sakamoto K, Murayama K, Takayanagi M, Hakamada K, Yasuda Y, Mizuta K. Wakiya T, et al. Among authors: takayanagi m. Mol Genet Metab. 2012 Mar;105(3):404-7. doi: 10.1016/j.ymgme.2011.12.019. Epub 2012 Jan 4. Mol Genet Metab. 2012. PMID: 22264779

2

Nitric oxide synthesis in ornithine transcarbamylase deficiency: possible involvement of low no synthesis in clinical manifestations of urea cycle defect.

Nagasaka H, Komatsu H, Ohura T, Sogo T, Inui A, Yorifuji T, Murayama K, Takayanagi M, Kikuta H, Kobayashi K. Nagasaka H, et al. Among authors: takayanagi m. J Pediatr. 2004 Aug;145(2):259-62. doi: 10.1016/j.jpeds.2004.05.033. J Pediatr. 2004. PMID: 15289781

3

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. Among authors: takayanagi m. Metabolism. 2009 Mar;58(3):278-82. doi: 10.1016/j.metabol.2008.09.025. Metabolism. 2009. PMID: 19217439

4

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. Among authors: takayanagi m. 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.

5

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: takayanagi m. 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

6

Efficacy of bezafibrate in two patients with mitochondrial trifunctional protein deficiency.

Suyama T, Shimura M, Fushimi T, Kuranobu N, Ichimoto K, Matsunaga A, Takayanagi M, Murayama K. Suyama T, et al. Among authors: takayanagi m. Mol Genet Metab Rep. 2020 May 30;24:100610. doi: 10.1016/j.ymgmr.2020.100610. eCollection 2020 Sep. Mol Genet Metab Rep. 2020. PMID: 32509533 Free PMC article.

7

Intractable secretory diarrhea in a Japanese boy with mitochondrial respiratory chain complex I deficiency.

Murayama K, Nagasaka H, Tsuruoka T, Omata Y, Horie H, Tregoning S, Thorburn DR, Takayanagi M, Ohtake A. Murayama K, et al. Among authors: takayanagi m. Eur J Pediatr. 2009 Mar;168(3):297-302. doi: 10.1007/s00431-008-0753-7. Epub 2008 Jun 17. Eur J Pediatr. 2009. PMID: 18560889

8

[Acute encephalopathy in inherited metabolic diseases].

Fujinami A, Murayama K, Takayanagi M. Fujinami A, et al. Among authors: takayanagi m. Nihon Rinsho. 2011 Mar;69(3):477-82. Nihon Rinsho. 2011. PMID: 21400842 Review. Japanese.

9

Expression analysis of two mutant human ornithine transcarbamylases in COS-7 cells.

Kogo T, Satoh Y, Kanazawa M, Yamamoto S, Takayanagi M, Ohtake A, Mori M, Niimi H. Kogo T, et al. Among authors: takayanagi m. J Hum Genet. 1998;43(1):54-8. doi: 10.1007/s100380050037. J Hum Genet. 1998. PMID: 9609999

10

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: takayanagi m. 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

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