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Mucopolysaccharidosis type I therapy

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Annals of Ophthalmology

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References

  • Cleary MA, Wraith JE. The presenting features of mucopolysaccharidosis type IH (Hurler syndrome). Acta Paediatr 1995;84:337–339.

    PubMed  CAS  Google Scholar 

  • Francois J. Ocular manifestations of the mucopolysaccharidoses. Ophthalmologica 1974;169:345–361

    Article  PubMed  CAS  Google Scholar 

  • Grewal SS, Wynn R, Abdenur JE, et al. Safety and efficacy of enzyme replacement therapy in combination with hematopoietic stem cell transplantation in Hurler syndrome. Genet Med 2005;7:143–146.

    Article  PubMed  CAS  Google Scholar 

  • Wraith JE. The first 5 years of clinical experience with laronidase enzyme replacement therapy for mucopolysaccharidosis I. Expert Opin Pharmacother 2005;6:489–506.

    Article  PubMed  CAS  Google Scholar 

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Murillo-Lopez, F.H. Mucopolysaccharidosis type I therapy. Ann Ophthalmol 37, 235–236 (2005). https://doi.org/10.1385/AO:37:4:235

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  • DOI: https://doi.org/10.1385/AO:37:4:235

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