Ohtake A - Search Results

1

Pyruvate therapy for Leigh syndrome due to cytochrome c oxidase deficiency.

Komaki H, Nishigaki Y, Fuku N, Hosoya H, Murayama K, Ohtake A, Goto Y, Wakamoto H, Koga Y, Tanaka M. Komaki H, et al. Among authors: ohtake a. Biochim Biophys Acta. 2010 Mar;1800(3):313-5. doi: 10.1016/j.bbagen.2009.07.008. Epub 2009 Jul 17. Biochim Biophys Acta. 2010. PMID: 19616603

2

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: ohtake a. 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

3

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

4

Children's toxicology from bench to bed--Liver Injury (4): Mitochondrial respiratory chain disorder and liver disease in children.

Murayama K, Ohtake A. Murayama K, et al. Among authors: ohtake a. J Toxicol Sci. 2009;34 Suppl 2:SP237-43. doi: 10.2131/jts.34.sp237. J Toxicol Sci. 2009. PMID: 19571475 Free article.

5

Liver-specific mitochondrial respiratory chain complex I deficiency in fatal influenza encephalopathy.

Arakawa C, Endo A, Kohira R, Fujita Y, Fuchigami T, Mugishima H, Ohtake A, Murayama K, Mori M, Miyata R, Hatai Y. Arakawa C, et al. Among authors: ohtake a. Brain Dev. 2012 Feb;34(2):115-7. doi: 10.1016/j.braindev.2011.03.002. Epub 2011 Mar 26. Brain Dev. 2012. PMID: 21441007

6

Fatal case of mitochondrial DNA depletion with severe asphyxia in a newborn.

Nakano Y, Murayama K, Tsuruoka T, Aizawa M, Nagasaka H, Horie H, Ohtake A, Saitou K. Nakano Y, et al. Among authors: ohtake a. Pediatr Int. 2011 Apr;53(2):240-2. doi: 10.1111/j.1442-200X.2010.03183.x. Pediatr Int. 2011. PMID: 21501307 No abstract available.

7

Neonatal lactic acidosis with methylmalonic aciduria due to novel mutations in the SUCLG1 gene.

Sakamoto O, Ohura T, Murayama K, Ohtake A, Harashima H, Abukawa D, Takeyama J, Haginoya K, Miyabayashi S, Kure S. Sakamoto O, et al. Among authors: ohtake a. Pediatr Int. 2011 Dec;53(6):921-5. doi: 10.1111/j.1442-200X.2011.03412.x. Pediatr Int. 2011. PMID: 21639866

8

Two Japanese patients with Leigh syndrome caused by novel SURF1 mutations.

Tanigawa J, Kaneko K, Honda M, Harashima H, Murayama K, Wada T, Takano K, Iai M, Yamashita S, Shimbo H, Aida N, Ohtake A, Osaka H. Tanigawa J, et al. Among authors: ohtake a. Brain Dev. 2012 Nov;34(10):861-5. doi: 10.1016/j.braindev.2012.02.007. Epub 2012 Mar 10. Brain Dev. 2012. PMID: 22410471

9

Metabolic autopsy with postmortem cultured fibroblasts in sudden unexpected death in infancy: diagnosis of mitochondrial respiratory chain disorders.

Yamamoto T, Emoto Y, Murayama K, Tanaka H, Kuriu Y, Ohtake A, Matoba R. Yamamoto T, et al. Among authors: ohtake a. Mol Genet Metab. 2012 Aug;106(4):474-7. doi: 10.1016/j.ymgme.2012.05.002. Epub 2012 May 11. Mol Genet Metab. 2012. PMID: 22658691

10

Case of an infant with hepatic cirrhosis caused by mitochondrial respiratory chain disorder.

Enkai S, Koinuma S, Ito R, Igaki J, Hasegawa Y, Murayama K, Ohtake A. Enkai S, et al. Among authors: ohtake a. Pediatr Int. 2013 Aug;55(4):e103-6. doi: 10.1111/ped.12098. Pediatr Int. 2013. PMID: 23910810

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