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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

126 related items for PubMed ID: 5444922

  • 1. Metabolic diseases: more clues from enzymes.
    Nature; 1970 May 16; 226(5246):596. PubMed ID: 5444922
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  • 2. Enzyme replacement in Fabry's disease, an inborn error of metabolism.
    Mapes CA, Anderson RL, Sweeley CC, Desnick RJ, Krivit W.
    Science; 1970 Sep 04; 169(3949):987-9. PubMed ID: 4914726
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  • 3. The adnormal biochemistry of inherited disorders of lipid metabolism.
    Brady RO.
    Fed Proc; 1973 Jun 04; 32(6):1660-7. PubMed ID: 4351098
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  • 14. Enzymatic aspects of sphingolipid degradation.
    Gatt S.
    Chem Phys Lipids; 1970 Oct 04; 5(1):235-49. PubMed ID: 4920305
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  • 15. Ganglioside GM2 storage diseases: hexosaminidase deficiencies in cultured fibroblasts.
    Okada S, Veath ML, Leroy J, O'Brien JS.
    Am J Hum Genet; 1971 Jan 04; 23(1):55-61. PubMed ID: 5581981
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  • 17. Partial deficiency of hexosaminidase component a in juvenile gm2-gangliosidosis.
    Suzuki Y, Suzuki K.
    Neurology; 1970 Sep 04; 20(9):848-51. PubMed ID: 5466454
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