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Plasma globotriaosylsphingosine (lysoGb3) could be a biomarker for Fabry disease with a Chinese hotspot late-onset mutation (IVS4+919G>A).
Liao HC, Huang YH, Chen YJ, Kao SM, Lin HY, Huang CK, Liu HC, Hsu TR, Lin SP, Yang CF, Fann CS, Chiu PC, Hsieh KS, Fu YC, Ke YY, Lin CY, Tsai FJ, Wang CH, Chao MC, Yu WC, Chiang CC, Niu DM. Liao HC, et al. Among authors: ke yy. Clin Chim Acta. 2013 Nov 15;426:114-20. doi: 10.1016/j.cca.2013.09.008. Epub 2013 Sep 19. Clin Chim Acta. 2013. PMID: 24055776 Free article.
Enzyme replacement therapy for mucopolysaccharidosis VI--experience in Taiwan.
Lin HY, Chen MR, Chuang CK, Chen CP, Lin DS, Chien YH, Ke YY, Tsai FJ, Pan HP, Lin SJ, Hwu WL, Niu DM, Lee NC, Lin SP. Lin HY, et al. Among authors: ke yy. J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S421-7. doi: 10.1007/s10545-010-9212-5. Epub 2010 Oct 6. J Inherit Metab Dis. 2010. PMID: 20924685
Congenital generalized lipodystrophy in Taiwan.
Hsu RH, Lin WD, Chao MC, Hsiao HP, Wong SL, Chiu PC, Chu SY, Ke YY, Lau BH, Chien YH, Hwu WL, Tsai FJ, Wang CH, Lee NC. Hsu RH, et al. Among authors: ke yy. J Formos Med Assoc. 2019 Jan;118(1 Pt 1):142-147. doi: 10.1016/j.jfma.2018.02.003. Epub 2018 Mar 1. J Formos Med Assoc. 2019. PMID: 29478747 Free article.
Genotype and phenotype studies of Lowe syndrome in three families in Taiwan.
Chen KJ, Wu HR, Chao MC, Chang TM, Chien JW, Chen M, Ma GC, Ke YY. Chen KJ, et al. Among authors: ke yy. Pediatr Neonatol. 2021 May;62(3):327-328. doi: 10.1016/j.pedneo.2021.01.012. Epub 2021 Feb 6. Pediatr Neonatol. 2021. PMID: 33745830 Free article. No abstract available.
90 results