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Use of a modified alpha-N-acetylgalactosaminidase in the development of enzyme replacement therapy for Fabry disease.
Tajima Y, Kawashima I, Tsukimura T, Sugawara K, Kuroda M, Suzuki T, Togawa T, Chiba Y, Jigami Y, Ohno K, Fukushige T, Kanekura T, Itoh K, Ohashi T, Sakuraba H. Tajima Y, et al. Among authors: togawa t. Am J Hum Genet. 2009 Nov;85(5):569-80. doi: 10.1016/j.ajhg.2009.09.016. Epub 2009 Oct 22. Am J Hum Genet. 2009. PMID: 19853240 Free PMC article.
Plasma globotriaosylsphingosine as a biomarker of Fabry disease.
Togawa T, Kodama T, Suzuki T, Sugawara K, Tsukimura T, Ohashi T, Ishige N, Suzuki K, Kitagawa T, Sakuraba H. Togawa T, et al. Mol Genet Metab. 2010 Jul;100(3):257-61. doi: 10.1016/j.ymgme.2010.03.020. Epub 2010 Apr 1. Mol Genet Metab. 2010. PMID: 20409739
Fabry disease in a Japanese population-molecular and biochemical characteristics.
Sakuraba H, Tsukimura T, Togawa T, Tanaka T, Ohtsuka T, Sato A, Shiga T, Saito S, Ohno K. Sakuraba H, et al. Among authors: togawa t. Mol Genet Metab Rep. 2018 Oct 26;17:73-79. doi: 10.1016/j.ymgmr.2018.10.004. eCollection 2018 Dec. Mol Genet Metab Rep. 2018. PMID: 30386727 Free PMC article.
398 results