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PUBMED FOR HANDHELDS

Journal Abstract Search

198 related items for PubMed ID: 6442777

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  • 2. The biochemistry of sphingolipid storage diseases.
    Sandhoff K.
    Angew Chem Int Ed Engl; 1977 May; 16(5):273-85. PubMed ID: 406814
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  • 9. Lysosomal storage diseases.
    Glew RH, Basu A, Prence EM, Remaley AT.
    Lab Invest; 1985 Sep; 53(3):250-69. PubMed ID: 2993742
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  • 11. Sphingolipid metabolism in neural tissues.
    Brady RO.
    Neurosci Res (N Y); 1969 Sep; 2(0):301-15. PubMed ID: 4950732
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  • 13. Enzymic diagnosis of sphingolipidoses.
    Suzuki K.
    Methods Enzymol; 1978 Sep; 50():456-88. PubMed ID: 26837
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  • 14. Fibroblast phosphodiesterase deficiency in Niemann-Pick disease.
    Fensom AH, Benson PF, Babarik AW, Grant AR, Jacobs L.
    Biochem Biophys Res Commun; 1977 Feb 07; 74(3):877-83. PubMed ID: 191016
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  • 15. Heritable catabolic and anabolic disorders of lipid metabolism.
    Brady RO.
    Metabolism; 1977 Mar 07; 26(3):329-45. PubMed ID: 13262
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  • 16. Inherited lipid storage diseases of the central nervous system.
    Percy AK, Shapiro LJ, Kaback MM.
    Curr Probl Pediatr; 1979 Sep 07; 9(11):1-51. PubMed ID: 117977
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  • 18. Basic findings and current developments in sphingolipidoses.
    Pilz H, Heipertz R, Seidel D.
    Hum Genet; 1979 Mar 12; 47(2):113-34. PubMed ID: 108196
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  • 19. Concentrations of an activator protein for sphingolipid hydrolysis in liver and brain samples from patients with lysosomal storage diseases.
    Inui K, Wenger DA.
    J Clin Invest; 1983 Nov 12; 72(5):1622-8. PubMed ID: 6415115
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  • 20. An enzymological approach to the lipidoses.
    Tallman JF, Pentchev PG, Brady RO.
    Enzyme; 1974 Nov 12; 18(1):136-49. PubMed ID: 4211795
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