Enzyme replacement therapy with idursulfase for mucopolysaccharidosis type II (Hunter syndrome)

Author:

da Silva Edina MK1,Strufaldi Maria Wany Louzada2,Andriolo Regis B3,Silva Laercio A4

Affiliation:

1. Universidade Federal de São Paulo; Emergency Medicine and Evidence Based Medicine; Rua Borges Lagoa 564 cj 64 Vl. Clementino São Paulo São Paulo Brazil 04038-000

2. Universidade Federal de São Paulo; São Paulo São Paulo Brazil

3. Universidade do Estado do Pará; Department of Public Health; Travessa Perebebuí, 2623 Belém Pará Brazil 66087-670

4. Universidade Federal de São Paulo; Department of Urology; Rua Doutor Nicolau de Sousa Queiros, 629. Ap.130B São Paulo São Paulo Brazil 04105002

Publisher

Wiley

Subject

Pharmacology (medical)

Reference37 articles.

1.  Long-term weekly dosing of idursulfase in the treatment of mucopolysaccharidosis II (MPS II, Hunter syndrome) [abstract];Beck;Journal of Inherited Metabolic Disease,2007

2. Long-term, open-labeled extension study of idursulfase in the treatment of Hunter syndrome;Muenzer;Genetics in Medicine,2011

3. Clinical benefit of enzyme replacement therapy (ERT) in mucopolysaccharidosis II (MPS II, Hunter syndrome) [abstract];Muenzer;Journal of Inherited Metabolic Disease,2006

4. A phase II/III clinical study of enzyme replacement therapy with idursulfase in mucopolysaccharidosis II (Hunter syndrome);Muenzer;Genetics in Medicine,2006

5. Clinical study of enzyme replacement therapy with idursulfase;Gutiérrez-Solana;Revista de Neurologia,2007

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