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High incidence of thrombosis in Fabry's disease.
Utsumi K, Yamamoto N, Kase R, Takata T, Okumiya T, Saito H, Suzuki T, Uyama E, Sakuraba H. Utsumi K, et al. Among authors: sakuraba h. Intern Med. 1997 May;36(5):327-9. doi: 10.2169/internalmedicine.36.327. Intern Med. 1997. PMID: 9213168 Free article.
[Fabry disease (alpha-galactosidase deficiency)].
Utsumi K, Sakuraba H. Utsumi K, et al. Among authors: sakuraba h. Ryoikibetsu Shokogun Shirizu. 1998;(19 Pt 2):367-71. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9645084 Review. Japanese. No abstract available.
[Fabry disease].
Sakuraba H. Sakuraba H. Ryoikibetsu Shokogun Shirizu. 2001;(33):661-2. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462619 Review. Japanese. No abstract available.
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: sakuraba h. 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. Among authors: sakuraba h. 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
Using imaging mass spectrometry to accurately diagnose Fabry's disease.
Onoue K, Zaima N, Sugiura Y, Isojima T, Okayama S, Horii M, Akai Y, Uemura S, Takemura G, Sakuraba H, Sakaguchi Y, Setou M, Saito Y. Onoue K, et al. Among authors: sakuraba h. Circ J. 2011;75(1):221-3. doi: 10.1253/circj.cj-10-0767. Epub 2010 Nov 28. Circ J. 2011. PMID: 21127380 Free article. No abstract available.
504 results