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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

175 related items for PubMed ID: 104554

  • 21.
    ; . PubMed ID:
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  • 22. Recent advances in the biochemistry and genetics of sphingolipidoses.
    Ozkara HA.
    Brain Dev; 2004 Dec; 26(8):497-505. PubMed ID: 15533650
    [Abstract] [Full Text] [Related]

  • 23. Metabolism of cerebroside sulphate and subcellular distribution of its metabolites in cultured skin fibroblasts derived from controls, metachromatic leukodystrophy, globoid cell leukodystrophy and Farber disease.
    Inui K, Furukawa M, Nishimoto J, Okada S, Yabuuchi H.
    J Inherit Metab Dis; 1987 Dec; 10(3):293-6. PubMed ID: 3123795
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  • 24.
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  • 25. [Lysosomal storage diseases: clinical variety and genetic heterogeneity (author's transl)].
    Gitzelmann R, Wiesmann UN, Spycher MA.
    Verh Dtsch Ges Pathol; 1976 Dec; ():101-5. PubMed ID: 828812
    [No Abstract] [Full Text] [Related]

  • 26. [Recent advances in sphingolipidosis research].
    Tamai Y, Kojima H.
    Tanpakushitsu Kakusan Koso; 1990 May; 35(7 Suppl):1291-303. PubMed ID: 1972585
    [No Abstract] [Full Text] [Related]

  • 27. Some inherited lysosomal enzyme defects with special reference to the liver and prospects for their control.
    Watts RW.
    Z Gastroenterol Verh; 1979 May; 16():137-43. PubMed ID: 95365
    [Abstract] [Full Text] [Related]

  • 28. From sheep to mice to cells: tools for the study of the sphingolipidoses.
    Zigdon H, Meshcheriakova A, Futerman AH.
    Biochim Biophys Acta; 2014 Aug; 1841(8):1189-99. PubMed ID: 24607565
    [Abstract] [Full Text] [Related]

  • 29.
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  • 30. Musculoskeletal manifestations of lysosomal storage disorders.
    Aldenhoven M, Sakkers RJ, Boelens J, de Koning TJ, Wulffraat NM.
    Ann Rheum Dis; 2009 Nov; 68(11):1659-65. PubMed ID: 19822711
    [Abstract] [Full Text] [Related]

  • 31. [Hereditary diseases related to a disorder in the breakdown of carbohydrate-containing compounds].
    Vidershaĭn GIa.
    Usp Sovrem Biol; 1974 Nov; 77(3):434-51. PubMed ID: 4278594
    [No Abstract] [Full Text] [Related]

  • 32. Lysosomal storage diseases in Greece.
    Michelakakis H, Dimitriou E, Tsagaraki S, Giouroukos S, Schulpis K, Bartsocas CS.
    Genet Couns; 1995 Nov; 6(1):43-7. PubMed ID: 7794561
    [Abstract] [Full Text] [Related]

  • 33.
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  • 34. Sphingolipid activator protein deficiency in a 16-week-old atypical Gaucher disease patient and his fetal sibling: biochemical signs of combined sphingolipidoses.
    Harzer K, Paton BC, Poulos A, Kustermann-Kuhn B, Roggendorf W, Grisar T, Popp M.
    Eur J Pediatr; 1989 Oct; 149(1):31-9. PubMed ID: 2514102
    [Abstract] [Full Text] [Related]

  • 35.
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  • 36.
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  • 37.
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  • 38. [Current aspects of the problem of thesaurismoses].
    Ivanovskaia TE, Leonova LV.
    Arkh Patol; 1981 Oct; 43(6):3-11. PubMed ID: 6791615
    [Abstract] [Full Text] [Related]

  • 39.
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  • 40.
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