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Volumn 129, Issue 1, 1996, Pages 145-148

Bone marrow transplantation in Hunter syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BONE MARROW TRANSPLANTATION; CASE REPORT; CENTRAL NERVOUS SYSTEM; CHILD; COGNITIVE DEFECT; ENZYME ACTIVITY; HUMAN; HUNTER SYNDROME; INBORN ERROR OF METABOLISM; MACROPHAGE FUNCTION; MALE; MUCOPOLYSACCHARIDOSIS; PHENOTYPE; PRIORITY JOURNAL; X CHROMOSOME LINKAGE;

EID: 0029795037     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(96)70202-0     Document Type: Article
Times cited : (89)

References (15)
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  • 2
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  • 3
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    • LH Rome B Weissmann EF Neufeld Direct demonstration of binding of a lysosomal enzyme iduronidase, to receptors on cultured fibroblasts Proc Natl Acad Sci USA 76 1979 2331 2334
    • (1979) Proc Natl Acad Sci USA , vol.76 , pp. 2331-2334
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  • 4
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    • The mucopolysaccharidoses: diagnosis, molecular genetics and treatment
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    • (1990) Mol Biol Med , vol.7 , pp. 381-404
    • Hopwood, JJ1    Morris, CP2
  • 5
    • 0008400290 scopus 로고
    • The mucopolysaccharidoses
    • J Spranger The mucopolysaccharidoses 2nd ed AH Emery DL Rimin JA Sofaer Principles and practice of medical genetics 1990 : Churchill-Livingstone New York 1797 1807
    • (1990) , pp. 1797-1807
    • Spranger, J1
  • 6
    • 0025850292 scopus 로고
    • Bone marrow transplantation for the treatment of genetic diseases
    • MJ Cowan Bone marrow transplantation for the treatment of genetic diseases Clin Biochem 24 1991 375 381
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    • Cowan, MJ1
  • 7
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    • The clinical phenotype of two patients with a complete deletion of the iduronate-2-sulfatase gene (MPS II-Hunter's syndrome)
    • JE Wraith A Cooper M Thornley RJ Willson PV Nelson CP Morris The clinical phenotype of two patients with a complete deletion of the iduronate-2-sulfatase gene (MPS II-Hunter's syndrome) Hum Genet 87 1991 205 206
    • (1991) Hum Genet , vol.87 , pp. 205-206
    • Wraith, JE1    Cooper, A2    Thornley, M3    Willson, RJ4    Nelson, PV5    Morris, CP6
  • 8
    • 0001924278 scopus 로고
    • Long-term follow-up of children with Hurler's disease treated with bone marrow transplantation
    • K Hugh-Jones JR Hobbs A Vellodi M Hancock J Sheldon S. Jones Long-term follow-up of children with Hurler's disease treated with bone marrow transplantation JR Hobbs Correction of certain genetic disorders by transplantation. 1989 : Cogent London 103 111
    • (1989) , pp. 103-111
    • Hugh-Jones, K1    Hobbs, JR2    Vellodi, A3    Hancock, M4    Sheldon, J5    Jones, S.6
  • 10
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    • Long-term effects of bone marrow transplantation for inborn errors of metabolism: a study of four patients with lysosomal storage diseases
    • M Imaizumi K Gushi I Kurobane S Inoye J Suzuki Y Koizumi Long-term effects of bone marrow transplantation for inborn errors of metabolism: a study of four patients with lysosomal storage diseases Acta Pediatr Jpn 36 1994 303 336
    • (1994) Acta Pediatr Jpn , vol.36 , pp. 303-336
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    • Long-term follow-up of a patient treated for Hunter disease type IIb: a case report and literature review
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    • (1994) Bone Marrow Transplant , vol.1 , pp. 653-658
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  • 13
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    • (1991) , pp. 206
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    • (1995) J Inherit Metab Dis , vol.18 , pp. 413-429
    • Shapiro, EG1    Lockman, LA2    Balthazor, M3    Krivit, W4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.