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Journal Abstract Search

260 related items for PubMed ID: 26943923

  • 1. Enzyme replacement therapy with galsulfase for mucopolysaccharidosis type VI.
    Brunelli MJ, Atallah ÁN, da Silva EM.
    Cochrane Database Syst Rev; 2016 Mar 04; 3():CD009806. PubMed ID: 26943923
    [Abstract] [Full Text] [Related]

  • 2. Enzyme replacement therapy with galsulfase for mucopolysaccharidosis type VI.
    Brunelli MJ, Atallah ÁN, da Silva EM.
    Cochrane Database Syst Rev; 2021 Sep 17; 9(9):CD009806. PubMed ID: 34533215
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  • 3. Enzyme replacement therapy outcomes across the disease spectrum: Findings from the mucopolysaccharidosis VI Clinical Surveillance Program.
    Harmatz PR, Lampe C, Parini R, Sharma R, Teles EL, Johnson J, Sivam D, Sisic Z.
    J Inherit Metab Dis; 2019 May 17; 42(3):519-526. PubMed ID: 30834539
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  • 4. Enzyme replacement therapy with idursulfase for mucopolysaccharidosis type II (Hunter syndrome).
    da Silva EM, Strufaldi MW, Andriolo RB, Silva LA.
    Cochrane Database Syst Rev; 2014 Jan 08; (1):CD008185. PubMed ID: 24399699
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  • 6. Enzyme replacement therapy with idursulfase for mucopolysaccharidosis type II (Hunter syndrome).
    da Silva EM, Strufaldi MW, Andriolo RB, Silva LA.
    Cochrane Database Syst Rev; 2011 Nov 09; (11):CD008185. PubMed ID: 22071845
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  • 7. Enzyme replacement therapy with idursulfase for mucopolysaccharidosis type II (Hunter syndrome).
    da Silva EM, Strufaldi MW, Andriolo RB, Silva LA.
    Cochrane Database Syst Rev; 2016 Feb 05; 2(2):CD008185. PubMed ID: 26845288
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  • 10. Enzyme replacement therapy with laronidase (Aldurazyme(®)) for treating mucopolysaccharidosis type I.
    Jameson E, Jones S, Remmington T.
    Cochrane Database Syst Rev; 2016 Apr 01; 4():CD009354. PubMed ID: 27033167
    [Abstract] [Full Text] [Related]

  • 11. Enzyme replacement therapy initiated in adulthood: Findings from the mucopolysaccharidosis VI Clinical Surveillance Program.
    Lampe C, Harmatz PR, Parini R, Sharma R, Teles EL, Johnson J, Sivam D, Sisic Z.
    Mol Genet Metab; 2019 Aug 01; 127(4):355-360. PubMed ID: 31324526
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  • 13. Natural history and galsulfase treatment in mucopolysaccharidosis VI (MPS VI, Maroteaux-Lamy syndrome)--10-year follow-up of patients who previously participated in an MPS VI Survey Study.
    Giugliani R, Lampe C, Guffon N, Ketteridge D, Leão-Teles E, Wraith JE, Jones SA, Piscia-Nichols C, Lin P, Quartel A, Harmatz P.
    Am J Med Genet A; 2014 Aug 01; 164A(8):1953-64. PubMed ID: 24764221
    [Abstract] [Full Text] [Related]

  • 14. Clinical effectiveness of enzyme replacement therapy with galsulfase in mucopolysaccharidosis type VI treatment: Systematic review.
    Gomes DF, Gallo LG, Leite BF, Silva RB, da Silva EN.
    J Inherit Metab Dis; 2019 Jan 01; 42(1):66-76. PubMed ID: 30740728
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  • 17. Enzyme replacement therapy for infantile-onset Pompe disease.
    Chen M, Zhang L, Quan S.
    Cochrane Database Syst Rev; 2017 Nov 20; 11(11):CD011539. PubMed ID: 29155436
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  • 19. Galsulfase: arylsulfatase B, BM 102, recombinant human arylsulfatase B, recombinant human N-acetylgalactosamine-4-sulfatase, rhASB.
    Drugs R D; 2005 Nov 20; 6(5):312-5. PubMed ID: 16128602
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