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Journal Abstract Search

114 related items for PubMed ID: 4213051

  • 1. Editorial: Therapy in genetic disease.
    Erbe RW.
    N Engl J Med; 1974 Nov 07; 291(19):1028-9. PubMed ID: 4213051
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  • 2. Enzyme replacement therapy in Gaucher's and Fabry's disease.
    Pentchev PG.
    Ann Clin Lab Sci; 1977 Nov 07; 7(3):251-3. PubMed ID: 404951
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  • 5. Further developments in studies in sphingolipidoses: "missing enzymes".
    Brady RO.
    Riv Patol Nerv Ment; 1970 Oct 07; 91(5):263-73. PubMed ID: 5525771
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  • 10. [Sphingolipidoses. Biochemistry and enzymatic mechanisms].
    Gajdos A.
    Nouv Presse Med; 1972 Jun 24; 1(26):1789-92. PubMed ID: 5054020
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  • 12. Repacement therapy in Gaucher disease.
    Beutler E, Dale GL, Kuhl W.
    Birth Defects Orig Artic Ser; 1980 Jun 24; 16(1):369-81. PubMed ID: 6778528
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  • 14. [Biochemical aspects of sphingolipidosis].
    Douste-Blazy L, Thouvenot JP.
    Ann Biol Clin (Paris); 1972 Jun 24; 30(6):623-35. PubMed ID: 4569435
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  • 15. Investigations in enzyme replacement therapy in lipid storage diseases.
    Brady RO, Pentchev PG, Gal AG.
    Fed Proc; 1975 Apr 24; 34(5):1310-5. PubMed ID: 804420
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  • 16. Chemical chaperones--a new concept in drug research.
    Kolter T, Wendeler M.
    Chembiochem; 2003 Apr 04; 4(4):260-4. PubMed ID: 12672104
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  • 20. Enzyme replacement in Fabry disease: treatment of cultured skin fibroblasts with a purified alpha-galactosidase from ficin.
    Dawson G, Matalon R, Li YT.
    Birth Defects Orig Artic Ser; 1973 Mar 04; 9(2):97-101. PubMed ID: 4215480
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