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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

130 related items for PubMed ID: 97112

  • 1. The pseudo-Hurler syndromes.
    Gordon N.
    Dev Med Child Neurol; 1978 Jun; 20(3):383-7. PubMed ID: 97112
    [No Abstract] [Full Text] [Related]

  • 2. Determination of lysosomal enzymes in saliva. Confirmation of the diagnosis of metachromatic leukodystrophy and fucosidosis by enzyme analysis.
    Den Tandt WR, Jaeken J.
    Clin Chim Acta; 1979 Sep 15; 97(1):19-25. PubMed ID: 40713
    [Abstract] [Full Text] [Related]

  • 3. Treatment related observations in solid tissues, fibroblast cultured and amniotic fluid cells of type II glycogenosis, Hurler disease and metachromatic leukodystrophy.
    Hug G, Schubert WK, Soukup S.
    Birth Defects Orig Artic Ser; 1973 Mar 15; 9(2):160-83. PubMed ID: 4215475
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  • 6. The mucopolysaccharidoses and mucolipidoses.
    Kelly TE.
    Clin Orthop Relat Res; 1976 Mar 15; (114):116-33. PubMed ID: 131015
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  • 8. High-performance liquid chromatographic analysis of oligosaccharides and glycopeptides accumulating in lysosomal storage disorders.
    Kin NM, Wolfe LS.
    Anal Biochem; 1980 Feb 15; 102(1):213-9. PubMed ID: 6766687
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  • 10. [Fucosidosis and mannosidosis].
    Arashima S.
    Nihon Rinsho; 1978 May 15; Suppl():1404-5. PubMed ID: 691371
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  • 13. Heritable catabolic and anabolic disorders of lipid metabolism.
    Brady RO.
    Metabolism; 1977 Mar 15; 26(3):329-45. PubMed ID: 13262
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  • 19. The occurrence of low alpha-L-fucosidase activities in normal human serum.
    Ramage P, Cunningham WL.
    Biochim Biophys Acta; 1975 Oct 22; 403(2):473-6. PubMed ID: 1182152
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