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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

167 related items for PubMed ID: 4211795

  • 21. Replacement therapy for inherited enzyme deficiency. Use of purified ceramidetrihexosidase in Fabry's disease.
    Brady RO, Tallman JF, Johnson WG, Gal AE, Leahy WR, Quirk JM, Dekaban AS.
    N Engl J Med; 1973 Jul 05; 289(1):9-14. PubMed ID: 4196713
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  • 25. Enzymic diagnosis of sphingolipidoses.
    Suzuki K.
    Methods Enzymol; 1978 Jul 05; 50():456-88. PubMed ID: 26837
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  • 26. [Inborn error of glycolipid metabolism].
    Suzuki Y.
    Horumon To Rinsho; 1975 Sep 05; 23(9):885-91. PubMed ID: 166
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  • 32. Multiple sulfatase deficiencies in cultured skin fibroblasts. Occurrence in patients with a variant form of metachromatic leukodystrophy.
    Eto Y, Wiesmann UN, Carson JH, Herschkowitz NN.
    Arch Neurol; 1974 Feb 05; 30(2):153-6. PubMed ID: 4272659
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  • 37. Hexosaminidase C in Tay-Sachs and Sandhoff disease.
    Penton E, Poenaru L, Dreyfus JC.
    Biochim Biophys Acta; 1975 May 23; 391(1):162-9. PubMed ID: 237554
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  • 38. Studies in Tay-Sachs and Sandhoff's diseases. Immunologic and structural properties of hexosaminidase A and hexosaminidase B.
    Beutler E, Srivastava SK.
    Isr J Med Sci; 1973 May 23; 9(9):1335-7. PubMed ID: 4798071
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  • 39. Disorders of lipid metabolism.
    Brady RO.
    Biochem Soc Symp; 1972 May 23; (35):113-27. PubMed ID: 4217183
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  • 40. Deficiency of lysosomal enzymes in storage diseases.
    Den Tandt WR, Giesberts MA.
    Biochem Med; 1973 Jun 23; 7(3):441-51. PubMed ID: 4268487
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