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Journal Abstract Search

135 related items for PubMed ID: 4268484

  • 21. Corrective factors for inborn errors of mucopolysaccharide metabolism.
    Neufeld EF, Cantz MJ.
    Ann N Y Acad Sci; 1971 Jul 06; 179():580-7. PubMed ID: 4255108
    [No Abstract] [Full Text] [Related]

  • 22. Deficiency of lysosomal enzymes in storage diseases.
    Den Tandt WR, Giesberts MA.
    Biochem Med; 1973 Jun 06; 7(3):441-51. PubMed ID: 4268487
    [No Abstract] [Full Text] [Related]

  • 23. Alpha-L-iduronidase activity in cultured skin fibroblasts and amniotic fluid cells.
    Hall CW, Neufeld EF.
    Arch Biochem Biophys; 1973 Oct 06; 158(2):817-21. PubMed ID: 4205743
    [No Abstract] [Full Text] [Related]

  • 24. Abnormal arylsulphatase activities of fibroblasts cultured from patients with mucopolysaccharidosis and cystinosis.
    Furusho K, Vetrella M, Latta E.
    Z Kinderheilkd; 1971 Oct 06; 110(4):324-31. PubMed ID: 4254863
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  • 26. Lysosomal enzymes in cultured cells from mucopolysaccharidoses.
    Keyser AJ, Priest RE, Priest JH.
    Lab Invest; 1972 Dec 06; 27(6):600-5. PubMed ID: 4264608
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  • 31. Beta-galactosidases in fibroblasts: Hurler and Sanfilippo syndromes.
    Benson PF, Bowser-Riley F, Giannelli F.
    N Engl J Med; 1970 Oct 29; 283(18):999-1000. PubMed ID: 4248669
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  • 32. Acid mucopolysaccharides in cultured human fibroblasts.
    Matalon R, Dorfman A.
    Lancet; 1969 Oct 18; 2(7625):838-41. PubMed ID: 4186295
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  • 33. Arylsulfatase B deficiency in Maroteaux-Lamy syndrome cultured fibroblasts.
    Fluharty AL, Stevens RL, Sanders DL, Kihara H.
    Biochem Biophys Res Commun; 1974 Jul 24; 59(2):455-61. PubMed ID: 4277366
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  • 34. The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase.
    Bach G, Eisenberg F, Cantz M, Neufeld EF.
    Proc Natl Acad Sci U S A; 1973 Jul 24; 70(7):2134-8. PubMed ID: 4269173
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  • 39. Urinary hyaluronidase activity in mucopolysaccharidosis.
    Józsa L, Szabó L.
    Acta Paediatr Acad Sci Hung; 1969 Jul 24; 10(1):73-8. PubMed ID: 4240053
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  • 40. Biochemical heterogeneity of the Sanfilippo syndrome: preliminary characterization of two deficient factors.
    Kresse H, Wiesmann U, Cantz M, Hall CW, Neufeld EF.
    Biochem Biophys Res Commun; 1971 Mar 05; 42(5):892-8. PubMed ID: 4252428
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