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Volumn 147, Issue 1, 2005, Pages 106-108

Mixed donor chimerism and low level iduronidase expression may be adequate for neurodevelopmental protection in Hurler syndrome

Author keywords

[No Author keywords available]

Indexed keywords

BUSULFAN; CYCLOPHOSPHAMIDE; LEVO IDURONIDASE;

EID: 22144442824     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpeds.2005.03.005     Document Type: Article
Times cited : (13)

References (11)
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    • The presenting features of mucopolysaccharidosis Type IH (Hurler Syndrome)
    • M.A. Cleary, and J.E. Wraith The presenting features of mucopolysaccharidosis Type IH (Hurler Syndrome) Acta Paediatric 84 1995 337 339
    • (1995) Acta Paediatric , vol.84 , pp. 337-339
    • Cleary, M.A.1    Wraith, J.E.2
  • 2
    • 0029146242 scopus 로고
    • Neuropsychological outcomes of several storage diseases with or without bone marrow transplant
    • E.G. Shapiro, L.A. Lockman, M. Balthazor, and W. Krivit Neuropsychological outcomes of several storage diseases with or without bone marrow transplant J Inher Metab Dis 18 1995 413 429
    • (1995) J Inher Metab Dis , vol.18 , pp. 413-429
    • Shapiro, E.G.1    Lockman, L.A.2    Balthazor, M.3    Krivit, W.4
  • 3
    • 2342666229 scopus 로고    scopus 로고
    • Enzyme replacement therapy for mucopolysaccharidosis I: A randomized, double-blinded, placebo-controlled, multinational study of recombinant human alpha-L-iduronidase
    • J.E. Wraith, L.A. Clarke, M. Beck, E.H. Kolodny, G.M. Pastores, and J. Muenzer Enzyme replacement therapy for mucopolysaccharidosis I: a randomized, double-blinded, placebo-controlled, multinational study of recombinant human alpha-L-iduronidase J Pediatrics 144 2004 581 588
    • (2004) J Pediatrics , vol.144 , pp. 581-588
    • Wraith, J.E.1    Clarke, L.A.2    Beck, M.3    Kolodny, E.H.4    Pastores, G.M.5    Muenzer, J.6
  • 4
    • 0032198225 scopus 로고    scopus 로고
    • Neuropsychological development of children with Hurler syndrome following hematopoietic stem cell transplant
    • C. Peters Neuropsychological development of children with Hurler syndrome following hematopoietic stem cell transplant Pediatr Transplant 2 1998 250 253
    • (1998) Pediatr Transplant , vol.2 , pp. 250-253
    • Peters, C.1
  • 5
    • 0032055564 scopus 로고    scopus 로고
    • Hurler syndrome: II. Outcome of HLA-genotypically identical sibling and HLA haploidentical related donor bone marrow transplantation in 54 children
    • C. Peters, E. Shapiro, J. Anderson, J.P. Henslee-Downey, M.R. Klemperer, and M.J. Cowan Hurler syndrome: II. Outcome of HLA-genotypically identical sibling and HLA haploidentical related donor bone marrow transplantation in 54 children Blood 7 1998 2601 2608
    • (1998) Blood , vol.7 , pp. 2601-2608
    • Peters, C.1    Shapiro, E.2    Anderson, J.3    Henslee-Downey, J.P.4    Klemperer, M.R.5    Cowan, M.J.6
  • 6
    • 9344245169 scopus 로고    scopus 로고
    • Outcome of unrelated donor bone marrow transplantation in 40 children with Hurler syndrome
    • C. Peters, M. Balthazor, E.G. Shapiro, J.R. King, C. Kollman, and J.D. Hegland Outcome of unrelated donor bone marrow transplantation in 40 children with Hurler syndrome Blood 87 1996 4894 4902
    • (1996) Blood , vol.87 , pp. 4894-4902
    • Peters, C.1    Balthazor, M.2    Shapiro, E.G.3    King, J.R.4    Kollman, C.5    Hegland, J.D.6
  • 7
    • 0032941197 scopus 로고    scopus 로고
    • Bone marrow transplant as effective treatment of central nervous system disease in globoid cell leukodystrophy, metachromatic leukodystrophy, adrenoleukodystrophy, mannosidosis, fucosidosis, aspartylglucosaminuria, Hurler, Marteaux-Lamy, and Sly syndromes and Gaucher disease type III
    • W. Krivit, C. Peters, and E.G. Shapiro Bone marrow transplant as effective treatment of central nervous system disease in globoid cell leukodystrophy, metachromatic leukodystrophy, adrenoleukodystrophy, mannosidosis, fucosidosis, aspartylglucosaminuria, Hurler, Marteaux-Lamy, and Sly syndromes and Gaucher disease type III Curr Opin Neurol 12 1999 167 176
    • (1999) Curr Opin Neurol , vol.12 , pp. 167-176
    • Krivit, W.1    Peters, C.2    Shapiro, E.G.3
  • 8
    • 0025850292 scopus 로고
    • Bone marrow transplant for the treatment of genetic disease
    • M.J. Cowan Bone marrow transplant for the treatment of genetic disease Clinical Biochemistry 24 1991 375 381
    • (1991) Clinical Biochemistry , vol.24 , pp. 375-381
    • Cowan, M.J.1
  • 9
    • 0031926575 scopus 로고    scopus 로고
    • Follow-up of nine patients with Hurler Syndrome after bone marrow transplant
    • N. Guffon, G. Souillet, I. Maire, J. Straczek, and P. Guibaud Follow-up of nine patients with Hurler Syndrome after bone marrow transplant J Pediatr 133 1998 119 125
    • (1998) J Pediatr , vol.133 , pp. 119-125
    • Guffon, N.1    Souillet, G.2    Maire, I.3    Straczek, J.4    Guibaud, P.5
  • 10
    • 0035090147 scopus 로고    scopus 로고
    • Evaluation of accumulated mucoploysaccharides in the brain if patients with mucopolysaccharidoses by H-magnetic resonance spectroscopy before and after bone marrow transplant
    • Y. Takakashi, K. Sukegawa, M. Aoki, K. Suzuki, H. Sakaguchi, and M. Watanabe Evaluation of accumulated mucoploysaccharides in the brain if patients with mucopolysaccharidoses by H-magnetic resonance spectroscopy before and after bone marrow transplant Pediatr Res 49 2001 349 355
    • (2001) Pediatr Res , vol.49 , pp. 349-355
    • Takakashi, Y.1    Sukegawa, K.2    Aoki, M.3    Suzuki, K.4    Sakaguchi, H.5    Watanabe, M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.