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Journal Abstract Search

165 related items for PubMed ID: 6778527

  • 1. An appraisal of human trials in enzyme replacement therapy of genetic diseases.
    Tager JM, Hamers MN, Schram AW, Van den Bergh FA, Rietra PJ, Loonen C, Koster JF, Slee R.
    Birth Defects Orig Artic Ser; 1980; 16(1):343-59. PubMed ID: 6778527
    [No Abstract] [Full Text] [Related]

  • 2. Lysosomal storage diseases.
    Brady RO.
    Pharmacol Ther; 1982; 19(3):327-36. PubMed ID: 6821325
    [No Abstract] [Full Text] [Related]

  • 3. [Enzyme deficiencies detected on cultured fibroblasts and amniotic cells. Application to prenatal diagnosis].
    Dreyfus JC, Poenaru L.
    Ann Biol Clin (Paris); 1975; 33(6):465-72. PubMed ID: 818927
    [Abstract] [Full Text] [Related]

  • 4. Genetic errors and enzyme replacement strategies.
    Brady RO.
    Res Publ Assoc Res Nerv Ment Dis; 1983; 60():181-93. PubMed ID: 6130585
    [No Abstract] [Full Text] [Related]

  • 5. Investigations in enzyme replacement therapy in lipid storage diseases.
    Brady RO, Pentchev PG, Gal AG.
    Fed Proc; 1975 Apr; 34(5):1310-5. PubMed ID: 804420
    [Abstract] [Full Text] [Related]

  • 6. [Enzyme replacement therapy for lysosomal storage disorders].
    Valayannopoulos V, Brassier A, Chabli A, Caillaud C, Lemoine M, Odent T, Arnoux JB, de Lonlay P.
    Arch Pediatr; 2011 Oct; 18(10):1119-23. PubMed ID: 21873040
    [Abstract] [Full Text] [Related]

  • 7. Editorial: Therapy in genetic disease.
    Erbe RW.
    N Engl J Med; 1974 Nov 07; 291(19):1028-9. PubMed ID: 4213051
    [No Abstract] [Full Text] [Related]

  • 8. Enzyme replacement for lysosomal diseases.
    Brady RO.
    Annu Rev Med; 2006 Nov 07; 57():283-96. PubMed ID: 16409150
    [Abstract] [Full Text] [Related]

  • 9. Enzyme replacement in Pompe disease with an alpha-glucosidase-low density lipoprotein complex.
    Williams JC, Murray AK.
    Birth Defects Orig Artic Ser; 1980 Nov 07; 16(1):415-23. PubMed ID: 7004520
    [No Abstract] [Full Text] [Related]

  • 10. [Macula findings in thesaurismoses].
    François J.
    Ber Zusammenkunft Dtsch Ophthalmol Ges; 1975 Nov 07; (73):223-65. PubMed ID: 54161
    [No Abstract] [Full Text] [Related]

  • 11. Common antigenicity for two glycosidases.
    Kakavanos R, Lehn P, Callebaut I, Meikle PJ, Parkinson-Lawrence EJ, Hopwood JJ, Brooks DA.
    FEBS Lett; 2006 Jan 09; 580(1):87-92. PubMed ID: 16359666
    [Abstract] [Full Text] [Related]

  • 12. Human trials: direct enzyme replacement--summary and discussion.
    Nadler HL.
    Birth Defects Orig Artic Ser; 1980 Jan 09; 16(1):425-6. PubMed ID: 7004521
    [No Abstract] [Full Text] [Related]

  • 13. [Use of the electron microscope in the diagnosis of various metabolic storage diseases].
    Porfiri B, Ricci R, Riccardi A, Segni G.
    Minerva Pediatr; 1982 Feb 28; 34(4):139-50. PubMed ID: 6806599
    [No Abstract] [Full Text] [Related]

  • 14. Genetic disorders of lysosomes.
    Hirschhorn R, Weissmann G.
    Prog Med Genet; 1976 Feb 28; 1():49-101. PubMed ID: 180565
    [No Abstract] [Full Text] [Related]

  • 15. Current status of treatment in storage disorders.
    Nadler HL.
    Birth Defects Orig Artic Ser; 1976 Feb 28; 12(6):177-88. PubMed ID: 10023
    [No Abstract] [Full Text] [Related]

  • 16. [Characteristics of biochemical disorders in hereditary enzymopathies in humans and animals].
    Rozenfel'd EL.
    Vopr Med Khim; 1982 Feb 28; 28(3):2-7. PubMed ID: 6125053
    [No Abstract] [Full Text] [Related]

  • 17. alpha-glucosidase (CHO) (Genzyme).
    Lachmann RH.
    Curr Opin Investig Drugs; 2004 Oct 28; 5(10):1101-10. PubMed ID: 15535432
    [Abstract] [Full Text] [Related]

  • 18. [Pompe's disease. Part II. Treatment strategies and enzyme replacement].
    Illés Z, Várdi Visy K.
    Ideggyogy Sz; 2009 Sep 30; 62(9-10):299-307. PubMed ID: 19835271
    [Abstract] [Full Text] [Related]

  • 19. The liver in lipid storage disease: biochemical basis of pathogenesis and clinical features.
    Brady RO, James SP, Barranger JA.
    Prog Liver Dis; 1982 Sep 30; 7():331-46. PubMed ID: 6810410
    [No Abstract] [Full Text] [Related]

  • 20. Enzyme replacement therapy in adult-onset glycogenosis II: is quantitative muscle MRI helpful?
    Pichiecchio A, Poloni GU, Ravaglia S, Ponzio M, Germani G, Maranzana D, Costa A, Repetto A, Tavazzi E, Danesino C, Moglia A, Bastianello S.
    Muscle Nerve; 2009 Jul 30; 40(1):122-5. PubMed ID: 19533640
    [Abstract] [Full Text] [Related]

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