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Journal Abstract Search

143 related items for PubMed ID: 6437709

  • 1. alpha-L-Iduronidase deficiency in mucopolysaccharidosis type I against a radiolabelled sulfated disaccharide substrate derived from dermatan sulfate.
    Muller VJ, Hopwood JJ.
    Clin Genet; 1984 Nov; 26(5):414-21. PubMed ID: 6437709
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  • 2. Selective depolymerisation of dermatan sulfate: production of radiolabelled substrates for alpha-L-iduronidase, sulfoiduronate sulfatase, and beta-D-glucuronidase.
    Hopwood JJ, Muller VJ.
    Carbohydr Res; 1983 Oct 28; 122(2):227-39. PubMed ID: 6423280
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  • 3. A fluorometric assay using 4-methylumbelliferyl alpha-L-iduronide for the estimation of alpha-L-iduronidase activity and the detection of Hurler and Scheie syndromes.
    Hopwood JJ, Muller V, Smithson A, Baggett N.
    Clin Chim Acta; 1979 Mar 01; 92(2):257-65. PubMed ID: 114339
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  • 4. alpha-L-iduronidase, beta-D-glucuronidase, and 2-sulfo-L-iduronate 2-sulfatase: preparation and characterization of radioactive substrates from heparin.
    Hopwood JJ.
    Carbohydr Res; 1979 Mar 01; 69():203-16. PubMed ID: 106967
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  • 5. Sulphamidase activity in leucocytes, cultured skin fibroblasts and amniotic cells: diagnosis of the Sanfilippo A syndrome with the use of radiolabelled disaccharide substrate.
    Hopwood JJ, Elliott H.
    Clin Sci (Lond); 1981 Dec 01; 61(6):729-35. PubMed ID: 6794973
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  • 10. Clinical ultrastructural and tissue culture studies in a possible compound Hurler-Scheie case.
    Tondeur M, Vamos-Hurwitz E, Cantz M, Cremer N, Libert J, Pardou A.
    Acta Paediatr Belg; 1976 Dec 01; 29(2):109-15. PubMed ID: 826105
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  • 11. A canine model of human alpha-L-iduronidase deficiency.
    Spellacy E, Shull RM, Constantopoulos G, Neufeld EF.
    Proc Natl Acad Sci U S A; 1983 Oct 01; 80(19):6091-5. PubMed ID: 6412235
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  • 16. Absence of alpha-L-iduronidase activity in various tissues from two sibs affected with presumably the Hurler-Scheie compound syndrome.
    Thompson JN, Finley SC, Lorincz AE, Finley WH.
    Birth Defects Orig Artic Ser; 1975 Oct 01; 11(6):341-6. PubMed ID: 811284
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  • 17. Use of 4-trifluoromethylumbelliferyl-alpha-L-iduronide as a new substrate for detection of alpha-L-iduronidase deficiency in human tissues and for rapid prenatal diagnosis of Hurler disease.
    Tsvetkova IV, Karpova EA, Voznyi YV, Zolotukhina TV, Biryukov VV, Semyachkina AN.
    J Inherit Metab Dis; 1991 Oct 01; 14(2):134-9. PubMed ID: 1909400
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  • 18. A radioactive substrate and assay for alpha-L-iduronidase.
    Di Natale P, Leder IG, Neufeld EF.
    Clin Chim Acta; 1977 Jun 15; 77(3):211-8. PubMed ID: 406106
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