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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

219 related items for PubMed ID: 6810572

  • 61. Lysosomal storage diseases.
    Lancet; 1986 Oct 18; 2(8512):898-9. PubMed ID: 2876331
    [No Abstract] [Full Text] [Related]

  • 62. [Metabolic disorders and corneal changes (author's transl)].
    François J.
    Klin Monbl Augenheilkd; 1981 Jun 18; 178(6):419-23. PubMed ID: 6973662
    [Abstract] [Full Text] [Related]

  • 63. [Clinical, genetic and biochemical study of a case of gargoylism].
    Lefebvre G, Duquennoy-Wanheuverswyn C.
    Pediatrie; 1965 Jun 18; 20(5):604-9. PubMed ID: 4954479
    [No Abstract] [Full Text] [Related]

  • 64. Variation in neuronal storage in alpha-L-iduronidase deficiency.
    Wassman ER.
    Am J Med Genet; 1985 Dec 18; 22(4):827-9. PubMed ID: 3934972
    [No Abstract] [Full Text] [Related]

  • 65. Trehalase deficiency in a family.
    Madzarovovà-Nohejlova J.
    Gastroenterology; 1973 Jul 18; 65(1):130-3. PubMed ID: 4737205
    [No Abstract] [Full Text] [Related]

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  • 73. Bone health in patients with inborn errors of metabolism.
    Langeveld M, Hollak CEM.
    Rev Endocr Metab Disord; 2018 Mar 18; 19(1):81-92. PubMed ID: 30209646
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  • 77. Lysosomal metabolism of glycoproteins.
    Winchester B.
    Glycobiology; 2005 Jun 18; 15(6):1R-15R. PubMed ID: 15647514
    [Abstract] [Full Text] [Related]

  • 78. [The contribution of the laboratory in the diagnosis of hereditary intermediate metabolism disorders].
    Khiari D, Tebib N, Kaabachi N, Ben Dridi MF, Mebazaa A.
    Tunis Med; 1995 May 18; 73(5):159-67. PubMed ID: 9507277
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