Author:
Augustine Erika F.,Mink Jonathan W.
Publisher
Springer Science and Business Media LLC
Reference77 articles.
1. Meikle PJ, Hopwood JJ, Clague AE, Carey WF. Prevalence of lysosomal storage disorders. JAMA. 1999;281:249–54.
2. Poupetova H, Ledvinova J, Berna L, Dvorakova L, Kozich V, Elleder M. The birth prevalence of lysosomal storage disorders in the Czech Republic: comparison with data in different populations. J Inherit Metab Dis. 2010;33:387–96.
3. Jurecka A, Żuber Z, Opoka-Winiarska V, Węgrzyn G, Tylki-Szymańska A. Effect of rapid cessation of enzyme replacement therapy: a report of 5 cases and a review of the literature. Mol Genet Metabol. 2012;107:508–12.
4. Wegrzyn G, Tylki-Szymanska A, Liberek A, Piotrowska E, Jakobkiewicz-Banecka J, Marucha J, et al. Rapid deterioration of a patient with mucopolysaccharidosis type I during interruption of enzyme replacement therapy. Am J Med Genet A. 2007;143A:1925–7.
5. Ratko TA, Marbella A, Godfrey S, Aronson N. Enzyme-Replacement Therapies for Lysosomal Storage Diseases. In: Technical Briefs, edn No. 12. Edited by Quality AfHRa. Rockville, MD: http://www.ncbi.nlm.nih.gov/books/NBK117214/ ; 2013.
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