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Page 1
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. Among authors: tajima g. Metabolism. 2010 Jan;59(1):107-13. doi: 10.1016/j.metabol.2009.07.013. Epub 2009 Sep 18. Metabolism. 2010. PMID: 19766269
Newborn screening for carnitine palmitoyltransferase II deficiency using (C16+C18:1)/C2: Evaluation of additional indices for adequate sensitivity and lower false-positivity.
Tajima G, Hara K, Tsumura M, Kagawa R, Okada S, Sakura N, Maruyama S, Noguchi A, Awaya T, Ishige M, Ishige N, Musha I, Ajihara S, Ohtake A, Naito E, Hamada Y, Kono T, Asada T, Sasai H, Fukao T, Fujiki R, Ohara O, Bo R, Yamada K, Kobayashi H, Hasegawa Y, Yamaguchi S, Takayanagi M, Hata I, Shigematsu Y, Kobayashi M. Tajima G, et al. Mol Genet Metab. 2017 Nov;122(3):67-75. doi: 10.1016/j.ymgme.2017.07.011. Epub 2017 Jul 31. Mol Genet Metab. 2017. PMID: 28801073
Stable-isotope dilution gas chromatography-mass spectrometric measurement of 3-hydroxyglutaric acid, glutaric acid and related metabolites in body fluids of patients with glutaric aciduria type 1 found in newborn screening.
Shigematsu Y, Hata I, Tanaka Y, Tajima G, Sakura N, Naito E, Yorifuji T. Shigematsu Y, et al. Among authors: tajima g. J Chromatogr B Analyt Technol Biomed Life Sci. 2005 Aug 25;823(1):7-12. doi: 10.1016/j.jchromb.2005.03.031. Epub 2005 Apr 18. J Chromatogr B Analyt Technol Biomed Life Sci. 2005. PMID: 16055049 Free article.
Surgical intervention for patent ductus venosus.
Kamimatsuse A, Onitake Y, Kamei N, Tajima G, Sakura N, Sueda T, Hiyama E. Kamimatsuse A, et al. Among authors: tajima g. Pediatr Surg Int. 2010 Oct;26(10):1025-30. doi: 10.1007/s00383-010-2662-x. Pediatr Surg Int. 2010. PMID: 20661579
Molecular pathogenesis of a novel mutation, G108D, in short-chain acyl-CoA dehydrogenase identified in subjects with short-chain acyl-CoA dehydrogenase deficiency.
Shirao K, Okada S, Tajima G, Tsumura M, Hara K, Yasunaga S, Ohtsubo M, Hata I, Sakura N, Shigematsu Y, Takihara Y, Kobayashi M. Shirao K, et al. Among authors: tajima g. Hum Genet. 2010 Jun;127(6):619-28. doi: 10.1007/s00439-010-0822-7. Epub 2010 Apr 8. Hum Genet. 2010. PMID: 20376488 Review.
147 results