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Page 1
Successful treatment of infantile-onset ACAD9-related cardiomyopathy with a combination of sodium pyruvate, beta-blocker, and coenzyme Q10.
Kadoya T, Sakakibara A, Kitayama K, Yamada Y, Higuchi S, Kawakita R, Kawasaki Y, Fujino M, Murakami Y, Shimura M, Murayama K, Ohtake A, Okazaki Y, Koga Y, Yorifuji T. Kadoya T, et al. Among authors: yorifuji t. J Pediatr Endocrinol Metab. 2019 Oct 25;32(10):1181-1185. doi: 10.1515/jpem-2019-0205. J Pediatr Endocrinol Metab. 2019. PMID: 31473688
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: yorifuji t. 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.
Relationship between oxidative stress and antioxidant systems in the liver of patients with Wilson disease: hepatic manifestation in Wilson disease as a consequence of augmented oxidative stress.
Nagasaka H, Inoue I, Inui A, Komatsu H, Sogo T, Murayama K, Murakami T, Yorifuji T, Asayama K, Katayama S, Uemoto S, Kobayashi K, Takayanagi M, Fujisawa T, Tsukahara H. Nagasaka H, et al. Among authors: yorifuji t. Pediatr Res. 2006 Oct;60(4):472-7. doi: 10.1203/01.pdr.0000238341.12229.d3. Epub 2006 Aug 28. Pediatr Res. 2006. PMID: 16940238
Molecular and clinical analysis of Japanese patients with persistent congenital hyperinsulinism: predominance of paternally inherited monoallelic mutations in the KATP channel genes.
Yorifuji T, Kawakita R, Nagai S, Sugimine A, Doi H, Nomura A, Masue M, Nishibori H, Yoshizawa A, Okamoto S, Doi R, Uemoto S, Nagasaka H. Yorifuji T, et al. J Clin Endocrinol Metab. 2011 Jan;96(1):E141-5. doi: 10.1210/jc.2010-1281. Epub 2010 Oct 13. J Clin Endocrinol Metab. 2011. PMID: 20943781
Experimental evidence that phenylalanine is strongly associated to oxidative stress in adolescents and adults with phenylketonuria.
Sanayama Y, Nagasaka H, Takayanagi M, Ohura T, Sakamoto O, Ito T, Ishige-Wada M, Usui H, Yoshino M, Ohtake A, Yorifuji T, Tsukahara H, Hirayama S, Miida T, Fukui M, Okano Y. Sanayama Y, et al. Among authors: yorifuji t. Mol Genet Metab. 2011 Jul;103(3):220-5. doi: 10.1016/j.ymgme.2011.03.019. Epub 2011 Mar 29. Mol Genet Metab. 2011. PMID: 21514861
487 results