메뉴 건너뛰기




Volumn 13, Issue 2, 2011, Pages 102-109

Idursulfase treatment of Hunter syndrome in children younger than 6 years: Results from the Hunter Outcome Survey

Author keywords

Hunter syndrome; idursulfase; safety

Indexed keywords

CREATININE; GLYCOSAMINOGLYCAN; IDURONATE 2 SULFATASE;

EID: 79951576876     PISSN: 10983600     EISSN: None     Source Type: Journal    
DOI: 10.1097/GIM.0b013e318206786f     Document Type: Article
Times cited : (81)

References (20)
  • 2
    • 0015798495 scopus 로고
    • The defect in the Hunter syndrome: Deficiency of sulfoiduronate sulfatase
    • Bach G, Eisenberg F Jr, Cantz M, Neufeld EF. The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase. Proc Natl Acad Sci USA 1973;70:2134-2138.
    • (1973) Proc Natl Acad Sci USA , vol.70 , pp. 2134-2138
    • Bach, G.1    Eisenberg Jr., F.2    Cantz, M.3    Neufeld, E.F.4
  • 5
    • 0020414447 scopus 로고
    • Mild form of Hunter's syndrome: Clinical delineation based on 31 cases
    • Young ID, Harper PS. Mild form of Hunter's syndrome: clinical delineation based on 31 cases. Arch Dis Child 1982;57:828-836. (Pubitemid 13238787)
    • (1982) Archives of Disease in Childhood , vol.57 , Issue.11 , pp. 828-836
    • Young, I.D.1    Harper, P.S.2
  • 6
    • 0020613358 scopus 로고
    • The natural history of the severe form of Hunter's syndrome: A study based on 52 cases
    • Young ID, Harper PS. The natural history of the severe form of Hunter's syndrome: a study based on 52 cases. Dev Med Child Neurol 1983;25:481-489. (Pubitemid 13030892)
    • (1983) Developmental Medicine and Child Neurology , vol.25 , Issue.4 , pp. 481-489
    • Young, I.D.1    Harper, P.S.2
  • 8
    • 33747209013 scopus 로고    scopus 로고
    • A phase II/III clinical study of enzyme replacement therapy with idursulfase in mucopolysaccharidosis II (Hunter syndrome)
    • Muenzer J, Wraith JE, Beck M, et al. A phase II/III clinical study of enzyme replacement therapy with idursulfase in mucopolysaccharidosis II (Hunter syndrome). Genet Med 2006;8:465-473.
    • (2006) Genet Med , vol.8 , pp. 465-473
    • Muenzer, J.1    Wraith, J.E.2    Beck, M.3
  • 9
    • 33846899175 scopus 로고    scopus 로고
    • A phase I/II clinical trial of enzyme replacement therapy in mucopolysaccharidosis II (Hunter syndrome)
    • DOI 10.1016/j.ymgme.2006.09.001, PII S1096719206002952
    • Muenzer J, Gucsavas-Calikoglu M, McCandless S, Schuetz T, Kimura A. A phase I/II clinical trial of enzyme replacement therapy in mucopolysaccharidosis II (Hunter syndrome). Mol Genet Metab 2007;90:329-337. (Pubitemid 46241902)
    • (2007) Molecular Genetics and Metabolism , vol.90 , Issue.3 SPEC. ISSUE , pp. 329-337
    • Muenzer, J.1    Gucsavas-Calikoglu, M.2    McCandless, S.E.3    Schuetz, T.J.4    Kimura, A.5
  • 10
    • 70349555987 scopus 로고    scopus 로고
    • 2000 CDC Growth Charts for the United States: Methods and development
    • Kuczmarski RJ, Ogden CL, Guo SS, et al. 2000 CDC Growth Charts for the United States: methods and development. Vital Health Stat 11 2002;1-190.
    • (2002) Vital Health Stat , vol.11 , pp. 1-190
    • Kuczmarski, R.J.1    Ogden, C.L.2    Guo, S.S.3
  • 11
    • 0020419764 scopus 로고
    • A clinical and genetic study of Hunter's syndrome. 2. Differences between the mild and severe forms
    • Young ID, Harper PS, Newcombe RG, Archer IM. A clinical and genetic study of Hunter's syndrome. 2. Differences between the mild and severe forms. J Med Genet 1982;19:408-411. (Pubitemid 13167537)
    • (1982) Journal of Medical Genetics , vol.19 , Issue.6 , pp. 408-411
    • Young, I.D.1    Harper, P.S.2    Newcombe, R.G.3    Archer, I.M.4
  • 12
    • 31544456336 scopus 로고    scopus 로고
    • Long-term therapy with agalsidase alfa for Fabry disease: Safety and effects on renal function in a home infusion setting
    • DOI 10.1093/ndt/gfi152
    • Schiffmann R, Ries M, Timmons M, Flaherty JT, Brady RO. Long-term therapy with agalsidase alfa for Fabry disease: safety and effects on renal function in a home infusion setting. Nephrol Dial Transplant 2006;21:345-354. (Pubitemid 43159987)
    • (2006) Nephrology Dialysis Transplantation , vol.21 , Issue.2 , pp. 345-354
    • Schiffmann, R.1    Ries, M.2    Timmons, M.3    Flaherty, J.T.4    Brady, R.O.5
  • 15
    • 33744978567 scopus 로고    scopus 로고
    • Enzyme replacement therapy for mucopolysaccharidosis VI: A phase 3, randomized, double-blind, placebo-controlled, multinational study of recombinant human N-acetylgalactosamine 4-sulfatase (recombinant human arylsulfatase B or rhASB) and follow-on, open-label extension study
    • Harmatz P, Giugliani R, Schwartz I, et al. Enzyme replacement therapy for mucopolysaccharidosis VI: a phase 3, randomized, double-blind, placebo-controlled, multinational study of recombinant human N-acetylgalactosamine 4-sulfatase (recombinant human arylsulfatase B or rhASB) and follow-on, open-label extension study. JPediatr 2006;148:533-539.
    • (2006) JPediatr , vol.148 , pp. 533-539
    • Harmatz, P.1    Giugliani, R.2    Schwartz, I.3
  • 17
    • 57449085309 scopus 로고    scopus 로고
    • A retrospective analysis of the potential impact of IgG antibodies to agalsidase beta on efficacy during enzyme replacement therapy for Fabry disease
    • Benichou B, Goyal S, Sung C, Norfleet AM, O'Brien F. A retrospective analysis of the potential impact of IgG antibodies to agalsidase beta on efficacy during enzyme replacement therapy for Fabry disease. Mol Genet Metab 2009;96:4-12.
    • (2009) Mol Genet Metab , vol.96 , pp. 4-12
    • Benichou, B.1    Goyal, S.2    Sung, C.3    Norfleet, A.M.4    O'Brien, F.5
  • 18
    • 71649090838 scopus 로고    scopus 로고
    • Japan Elaprase Treatment (JET) study: Idursulfase enzyme replacement therapy in adult patients with attenuated Hunter syndrome (mucopolysaccharidosis II, MPS II)
    • Okuyama T, Tanaka A, Suzuki Y, et al. Japan Elaprase Treatment (JET) study: idursulfase enzyme replacement therapy in adult patients with attenuated Hunter syndrome (mucopolysaccharidosis II, MPS II). Mol Genet Metab 2010;99:18-25.
    • (2010) Mol Genet Metab , vol.99 , pp. 18-25
    • Okuyama, T.1    Tanaka, A.2    Suzuki, Y.3
  • 19
    • 67649239047 scopus 로고    scopus 로고
    • The management of children with Hunter syndrome-A case study
    • Little C, Gould R, Hendriksz C. The management of children with Hunter syndrome-a case study. Br J Nursing 2009;18:321-322.
    • (2009) Br J Nursing , vol.18 , pp. 321-322
    • Little, C.1    Gould, R.2    Hendriksz, C.3
  • 20
    • 43049175045 scopus 로고    scopus 로고
    • Early response to idursulfase treatment in a 3 year-old boy affected of Hunter syndrome
    • Galan-Gomez E, Guerrero-Rico A, Caceres-Marzal C, et al. Early response to idursulfase treatment in a 3 year-old boy affected of Hunter syndrome. Eur J Med Genet 2008;51:268-271.
    • (2008) Eur J Med Genet , vol.51 , pp. 268-271
    • Galan-Gomez, E.1    Guerrero-Rico, A.2    Caceres-Marzal, C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.