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Mannose receptor-mediated delivery of moss-made α-galactosidase A efficiently corrects enzyme deficiency in Fabry mice.
Shen JS, Busch A, Day TS, Meng XL, Yu CI, Dabrowska-Schlepp P, Fode B, Niederkrüger H, Forni S, Chen S, Schiffmann R, Frischmuth T, Schaaf A. Shen JS, et al. Among authors: schiffmann r. J Inherit Metab Dis. 2016 Mar;39(2):293-303. doi: 10.1007/s10545-015-9886-9. Epub 2015 Aug 27. J Inherit Metab Dis. 2016. PMID: 26310963 Free PMC article.
Enzyme replacement therapy in Fabry disease.
Brady RO, Murray GJ, Moore DF, Schiffmann R. Brady RO, et al. Among authors: schiffmann r. J Inherit Metab Dis. 2001;24 Suppl 2:18-24; discussion 11-2. doi: 10.1023/a:1012451320105. J Inherit Metab Dis. 2001. PMID: 11758675 Review.
Fabry disease.
Schiffmann R. Schiffmann R. Pharmacol Ther. 2009 Apr;122(1):65-77. doi: 10.1016/j.pharmthera.2009.01.003. Epub 2009 Feb 8. Pharmacol Ther. 2009. PMID: 19318041 Review.
Management of neuronopathic Gaucher disease: revised recommendations.
Vellodi A, Tylki-Szymanska A, Davies EH, Kolodny E, Bembi B, Collin-Histed T, Mengel E, Erikson A, Schiffmann R. Vellodi A, et al. Among authors: schiffmann r. J Inherit Metab Dis. 2009 Oct;32(5):660-664. doi: 10.1007/s10545-009-1164-2. Epub 2009 Aug 5. J Inherit Metab Dis. 2009. PMID: 19655269
Biomarkers of Fabry disease nephropathy.
Schiffmann R, Waldek S, Benigni A, Auray-Blais C. Schiffmann R, et al. Clin J Am Soc Nephrol. 2010 Feb;5(2):360-4. doi: 10.2215/CJN.06090809. Epub 2009 Nov 5. Clin J Am Soc Nephrol. 2010. PMID: 19965549
322 results