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PUBMED FOR HANDHELDS

Journal Abstract Search


181 related items for PubMed ID: 805007

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  • 4. Pseudo-Hurler polydystrophy (mucolipidosis 3). A clinical, biochemical and ultrastructural study.
    Stein H, Berman ER, Livni N, Merin S, Sheskin J, Cohen T.
    Isr J Med Sci; 1974 May; 10(5):463-75. PubMed ID: 4213328
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  • 5. Properties of alpha-L-iduronidase in cultured skin fibroblasts from alpha-L-iduronidase-deficient patients.
    Fujibayashi S, Minami R, Ishikawa Y, Wagatsuma K, Nakao T, Tsugawa S.
    Hum Genet; 1984 May; 65(3):268-72. PubMed ID: 6421718
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  • 7. Simplied assay method of alpha-L-iduronidase activity in leukocytes for detection of Hurler syndrome and its carriers.
    Momoi T, Sudo M, Tanioka KI, Kushida H.
    Clin Chim Acta; 1977 Dec 15; 81(3):311-3. PubMed ID: 411615
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  • 8. 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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  • 11. Beta-glucuronidase deficiency mucopolysaccharidosis: methods for enzymatic diagnosis.
    Glaser JH, Sly WS.
    J Lab Clin Med; 1973 Dec 01; 82(6):969-77. PubMed ID: 4202279
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  • 14. [Fluorometric determination of alpha-L-iduronidase activity in leukocytes and blood plasma in Hurler's disease].
    Gusina NB, Tsukerman GL.
    Lab Delo; 1988 Dec 01; (7):46-9. PubMed ID: 2460681
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  • 18. Apparent allelism of the Hurler, Scheie, and Hurler/Scheie syndromes.
    Mueller OT, Shows TB, Opitz JM.
    Am J Med Genet; 1984 Jul 01; 18(3):547-56. PubMed ID: 6433708
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  • 20. 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 Jul 01; 29(2):109-15. PubMed ID: 826105
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