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Novel heparan sulfate assay by using automated high-throughput mass spectrometry: Application to monitoring and screening for mucopolysaccharidoses.
Shimada T, Kelly J, LaMarr WA, van Vlies N, Yasuda E, Mason RW, Mackenzie W, Kubaski F, Giugliani R, Chinen Y, Yamaguchi S, Suzuki Y, Orii KE, Fukao T, Orii T, Tomatsu S. Shimada T, et al. Among authors: suzuki y. Mol Genet Metab. 2014 Sep-Oct;113(1-2):92-9. doi: 10.1016/j.ymgme.2014.07.008. Epub 2014 Jul 21. Mol Genet Metab. 2014. PMID: 25092413 Free PMC article.
Peroxisomal acyl CoA oxidase deficiency.
Suzuki Y, Iai M, Kamei A, Tanabe Y, Chida S, Yamaguchi S, Zhang Z, Takemoto Y, Shimozawa N, Kondo N. Suzuki Y, et al. J Pediatr. 2002 Jan;140(1):128-30. doi: 10.1067/mpd.2002.120511. J Pediatr. 2002. PMID: 11815777
Epidemiology of X-linked adrenoleukodystrophy in Japan.
Takemoto Y, Suzuki Y, Tamakoshi A, Onodera O, Tsuji S, Hashimoto T, Shimozawa N, Orii T, Kondo N. Takemoto Y, et al. Among authors: suzuki y. J Hum Genet. 2002;47(11):590-3. doi: 10.1007/s100380200090. J Hum Genet. 2002. PMID: 12436195
Development and testing of new screening method for keratan sulfate in mucopolysaccharidosis IVA.
Tomatsu S, Okamura K, Taketani T, Orii KO, Nishioka T, Gutierrez MA, Velez-Castrillon S, Fachel AA, Grubb JH, Cooper A, Thornley M, Wraith E, Barrera LA, Giugliani R, Schwartz IV, Frenking GS, Beck M, Kircher SG, Paschke E, Yamaguchi S, Ullrich K, Isogai K, Suzuki Y, Orii T, Kondo N, Creer M, Noguchi A. Tomatsu S, et al. Among authors: suzuki y. Pediatr Res. 2004 Apr;55(4):592-7. doi: 10.1203/01.PDR.0000113767.60140.E9. Epub 2004 Jan 7. Pediatr Res. 2004. PMID: 14711889
Portal hypertension in a patient with Hunter disease.
Kato T, Isogai K, Orii K, Kuratsubo I, Kondo N, Orii T, Suzuki Y. Kato T, et al. Among authors: suzuki y. J Inherit Metab Dis. 2006 Oct;29(5):686. doi: 10.1007/s10545-006-0308-x. Epub 2006 Aug 5. J Inherit Metab Dis. 2006. PMID: 16972178
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