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Journal Abstract Search

322 related items for PubMed ID: 4202279

  • 1. Beta-glucuronidase deficiency mucopolysaccharidosis: methods for enzymatic diagnosis.
    Glaser JH, Sly WS.
    J Lab Clin Med; 1973 Dec; 82(6):969-77. PubMed ID: 4202279
    [No Abstract] [Full Text] [Related]

  • 2. 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
    [No Abstract] [Full Text] [Related]

  • 3. [Proceedings: Fluorimetric determination of some enzymes in leukocytes involved in metabolic disorders].
    Marchesini S, Di Donato S, Tettamanti G, Zambotti V.
    Quad Sclavo Diagn; 1973 Mar; 9(1):472-83. PubMed ID: 4788724
    [No Abstract] [Full Text] [Related]

  • 4. Macular cherry-red spot, corneal clouding, and beta-galactosidase deficiency. Clinical, biochemical, and electron microscopic study of a new autosomal recessive storage disease.
    Goldberg MF, Cotlier E, Fichenscher LG, Kenyon K, Enat R, Borowsky SA.
    Arch Intern Med; 1971 Sep; 128(3):387-98. PubMed ID: 4999185
    [No Abstract] [Full Text] [Related]

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  • 8. Acid hydrolases in skin and plasma in gargoylism. Deficiency of beta-galactosidase in skin.
    Ockerman PA.
    Clin Chim Acta; 1968 Apr; 20(1):1-6. PubMed ID: 4967992
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  • 10. [Enzyme deficiencies detected on cultured fibroblasts and amniotic cells. Application to prenatal diagnosis].
    Dreyfus JC, Poenaru L.
    Ann Biol Clin (Paris); 1975 Apr; 33(6):465-72. PubMed ID: 818927
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  • 11. Deficiency of lysosomal enzymes in storage diseases.
    Den Tandt WR, Giesberts MA.
    Biochem Med; 1973 Jun; 7(3):441-51. PubMed ID: 4268487
    [No Abstract] [Full Text] [Related]

  • 12. Beta-glucuronidase deficiency mucopolysaccharidosis.
    Sly WS, Brot FE, Glaser J, Stahl PD, Quinton BA, Rimoin DL, McAlister WH.
    Birth Defects Orig Artic Ser; 1974 Jun; 10(12):239-45. PubMed ID: 4282258
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  • 15. Diagnosis of the mucopolysaccharidoses using cultured skin fibroblasts and amniotic fluid cells.
    Butterworth J.
    J Inherit Metab Dis; 1978 Jun; 1(1):25-8. PubMed ID: 117232
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  • 17. Mucopolysaccharide storage diseases and lysosomal hydrolases in cultured fibroblasts.
    den Tandt WR, Schaberg A.
    Pathol Eur; 1973 Jun; 8(1):3-11. PubMed ID: 4269628
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  • 18. 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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