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laronidase journal articles from PubMed MEDLINE database

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Cimaz R, Coppa GV, Kone-Paut I, et al. 
Joint contractures in the absence of inflammation may indicate mucopolysaccharidosis. [JOURNAL ARTICLE]
Pediatr Rheumatol Online J 2009 Oct 23; 7(1):18.
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Tylki-Szymanska A, Rozdzynska A, Jurecka A, et al. 
Anthropometric data of 14 patients with mucopolysaccharidosis I: Retrospective analysis and efficacy of recombinant human alpha-l-iduronidase (laronidase). [JOURNAL ARTICLE]
Mol Genet Metab 2009 Aug 27.
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Yano S, Moseley K, Pavlova Z 
Postmortem studies on a patient with mucopolysaccharidosis type I: Histopathological findings after one year of enzyme replacement therapy. [JOURNAL ARTICLE]
J Inherit Metab Dis 2009 Mar 27.
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Wynn RF, Mercer J, Page J, et al. 
Use of enzyme replacement therapy (Laronidase) before hematopoietic stem cell transplantation for mucopolysaccharidosis I: experience in 18 patients. [Journal Article, Research Support, Non-U.S. Gov't]
J Pediatr 2009 Jan; 154(1):135-9.
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Clarke LA, Wraith JE, Beck M, et al. 
Long-term efficacy and safety of laronidase in the treatment of mucopolysaccharidosis I. [Journal Article]
Pediatrics 2009 Jan; 123(1):229-40.
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Giugliani R, Rojas VM, Martins AM, et al. 
A dose-optimization trial of laronidase (Aldurazyme) in patients with mucopolysaccharidosis I. [Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't]
Mol Genet Metab 2009 Jan; 96(1):13-9.
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Munoz-Rojas MV, Vieira T, Costa R, et al. 
Intrathecal enzyme replacement therapy in a patient with mucopolysaccharidosis type I and symptomatic spinal cord compression. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Sep 15.
Abstract | Full Citation
Tsukimura T, Tajima Y, Kawashima I, et al. 
Uptake of a Recombinant Human alpha-L-Iduronidase (laronidase) by Cultured Fibroblasts and Osteoblasts. [JOURNAL ARTICLE]
Biol Pharm Bull 2008; 31(9):1691-1695.
Abstract | Full Citation
Pastores GM 
Laronidase (Aldurazyme): enzyme replacement therapy for mucopolysaccharidosis type I. [Journal Article]
Expert Opin Biol Ther 2008 Jul; 8(7):1003-9.
Abstract | Full Citation
Cáceres-Marzal C, García-Reymundo M, Solana J, et al. 
Decreased corneal opacity and improved vision in a patient with mucopolysaccharidosis I (Hurler-Scheie) treated with enzyme replacement therapy (laronidase, Aldurazyme(R)). [JOURNAL ARTICLE]
Am J Med Genet A 2008 Jun 10.
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