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PUBMED FOR HANDHELDS

Journal Abstract Search


189 related items for PubMed ID: 4678225

  • 21. Farber's lipogranulomatosis: ceramidase deficiency and prolonged survival in three relatives.
    Pavone L, Moser HW, Mollica F, Reitano C, Durand P.
    Johns Hopkins Med J; 1980 Nov; 147(5):193-6. PubMed ID: 7441940
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  • 24. Enzymatic aspects of sphingolipid degradation.
    Gatt S.
    Chem Phys Lipids; 1970 Oct; 5(1):235-49. PubMed ID: 4920305
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  • 29. [Farber's lipogranulomatosis].
    Barrière H, Gillot F.
    Nouv Presse Med; 1972 Mar; 2(12):767-70. PubMed ID: 4145224
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  • 33. Editorial: The use of tears for heterozygote detection and genetic counseling.
    Goldberg MF.
    Invest Ophthalmol; 1974 Mar; 13(3):159-60. PubMed ID: 4205146
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  • 35. Beta-galactosidase deficiency in the hurler syndrome.
    MacBrinn M, Okada S, Woollacott M, Patel V, Ho MW, Tappel AL, O'Brien JS.
    N Engl J Med; 1969 Aug 14; 281(7):338-43. PubMed ID: 4240150
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  • 36. Acid hydrolases in the serum and liver in mucopolysaccharidoses types I and 3.
    Gordon BA, Feleki V.
    Clin Biochem; 1970 Sep 14; 3(3):193-202. PubMed ID: 4258597
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