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Journal Abstract Search

135 related items for PubMed ID: 4268484

  • 1. -Galactosidase, N-acetyl- -glucosaminidase, and -glucuronidase activity in fibroblast cultures from patients with mucopolysaccharide storage disease.
    Lagunoff D, Pritzl P, Scott CR.
    Biochem Med; 1973 Jun; 7(3):343-9. PubMed ID: 4268484
    [No Abstract] [Full Text] [Related]

  • 2. Acid glycosidases in mucopolysaccharidoses fibroblasts.
    Fluharty AL, Porter MT, Lassila EL, Trammell J, Carrel RE, Kihara H.
    Biochem Med; 1970 Sep; 4(2):110-20. PubMed ID: 4257448
    [No Abstract] [Full Text] [Related]

  • 3. Inborn errors of mucopolysaccharide metabolism.
    Neufeld EF, Fratantoni JC.
    Science; 1970 Jul 10; 169(3941):141-6. PubMed ID: 4246678
    [No Abstract] [Full Text] [Related]

  • 4. Simulation of genetic mucopolysaccharidoses in normal human fibroblasts by alteration of pH of the medium.
    Lie SO, McKusick VA, Neufeld EF.
    Proc Natl Acad Sci U S A; 1972 Sep 10; 69(9):2361-3. PubMed ID: 4262638
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  • 5. Mucopolysaccharidosis: secondarily induced abnormal distribution of lysosomal isoenzymes.
    Kint JA, Dacremont G, Carton D, Orye E, Hooft C.
    Science; 1973 Jul 27; 181(4097):352-4. PubMed ID: 4268963
    [Abstract] [Full Text] [Related]

  • 6. Leroy's l-cell disease: markedly increased activity of plasma acid hydrolases.
    Den Tandt WR, Lassila E, Philippart M.
    J Lab Clin Med; 1974 Mar 27; 83(3):403-8. PubMed ID: 4359899
    [No Abstract] [Full Text] [Related]

  • 7. Corneal clouding in the genetic mucopolysaccharidoses: a cell culture study.
    Danes BS.
    Clin Genet; 1973 Mar 27; 4(1):1-7. PubMed ID: 4266264
    [No Abstract] [Full Text] [Related]

  • 8. A recognition marker required for uptake of a lysosomal enzyme by cultured fibroblasts.
    Hickman S, Shapiro LJ, Neufeld EF.
    Biochem Biophys Res Commun; 1974 Mar 15; 57(1):55-61. PubMed ID: 4364008
    [No Abstract] [Full Text] [Related]

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  • 10. Enzyme patterns in tissues and body fluids in mucopolysaccharidoses.
    Ockerman PA, Hultberg B, Eriksson O.
    Clin Chim Acta; 1969 Jul 15; 25(1):97-102. PubMed ID: 4240390
    [No Abstract] [Full Text] [Related]

  • 11. Glycosaminoglycans. A biochemical and clinical review.
    Lamberg SI, Stoolmiller AC.
    J Invest Dermatol; 1974 Dec 15; 63(6):433-49. PubMed ID: 4139221
    [No Abstract] [Full Text] [Related]

  • 12. Mucopolysaccharide storage diseases and lysosomal hydrolases in cultured fibroblasts.
    den Tandt WR, Schaberg A.
    Pathol Eur; 1973 Dec 15; 8(1):3-11. PubMed ID: 4269628
    [No Abstract] [Full Text] [Related]

  • 13. Enzyme defects of glycosaminoglycan degradation in the mucopolysaccharidoses.
    Benson PF.
    Dev Med Child Neurol; 1974 Aug 15; 16(4):534-9. PubMed ID: 4277471
    [No Abstract] [Full Text] [Related]

  • 14. [Recent data on mucopolysaccharidoses].
    Spranger J.
    Monatsschr Kinderheilkd (1902); 1973 May 15; 121(5):181-3. PubMed ID: 4268292
    [No Abstract] [Full Text] [Related]

  • 15. Sanfilippo syndrome: profound deficiency of alpha-acetylglucosaminidase activity in organs and skin fibroblasts from type-B patients.
    O'Brien JS.
    Proc Natl Acad Sci U S A; 1972 Jul 15; 69(7):1720-2. PubMed ID: 4261742
    [Abstract] [Full Text] [Related]

  • 16. [Hereditary mucopolysaccharidoses (literature survey)].
    Pashin IuV.
    Vopr Okhr Materin Det; 1972 Jun 15; 17(6):49-52. PubMed ID: 4262644
    [No Abstract] [Full Text] [Related]

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  • 20. Sanfilippo disease type B: enzyme replacement and metabolic correction in cultured fibroblasts.
    O'Brien JS, Miller AL, Loverde AW, Veath ML.
    Science; 1973 Aug 24; 181(4101):753-5. PubMed ID: 4269326
    [Abstract] [Full Text] [Related]

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