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PUBMED FOR HANDHELDS

Journal Abstract Search


158 related items for PubMed ID: 6438393

  • 1. Metabolism of collagen in aspartylglycosaminuria: urinary excretion of hydroxyproline.
    Näntö-Salonen K, Autio S, Härö E, Kivimäki T, Koskela SL, Näntö V, Penttinen R.
    J Inherit Metab Dis; 1984; 7(3):117-21. PubMed ID: 6438393
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  • 3. Metabolism of collagen in aspartylglycosaminuria: decreased synthesis by cultured fibroblasts.
    Näntö-Salonen K, Penttinen R.
    J Inherit Metab Dis; 1982; 5(4):197-203. PubMed ID: 6820441
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  • 5. Aspartylglycosaminuria: an inborn error of glycoprotein catabolism.
    Maury CP.
    J Inherit Metab Dis; 1982; 5(4):192-6. PubMed ID: 6820440
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  • 6. Abnormal collagen fibrils in aspartylglycosaminuria. Altered dermal ultrastructure in a glycoprotein storage disorder.
    Näntö-Salonen K, Pelliniemi LJ, Autio S, Kivimäki T, Rapola J, Penttinen R.
    Lab Invest; 1984 Oct; 51(4):464-8. PubMed ID: 6592395
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  • 7. Abnormal dermal proteoglycan in aspartylglycosaminuria: a possible mechanism for ultrastructural changes of collagen fibrils in a glycoprotein storage disorder.
    Näntö-Salonen K, Larjava H, Säämanen AM, Heino J, Penttinen R, Pelliniemi LJ, Tammi M.
    Connect Tissue Res; 1987 Oct; 16(4):367-76. PubMed ID: 3132350
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  • 9. Aspartylglycosaminuria in Northern Norway in eight patients: clinical heterogeneity and variations with the diet.
    Borud O, Strömme JH, Lie SO, Torp KH.
    J Inherit Metab Dis; 1978 Oct; 1(3):95-7. PubMed ID: 116085
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  • 11. [The influence of diet on the urinary excretion of total, free and conjugated non-dialysable hydroxyproline in the normal adult (author's transl)].
    Pilonchery G, Finck C, Minaire P, Messy P, Revol A.
    Ann Biol Clin (Paris); 1982 Oct; 40(1):17-22. PubMed ID: 7081785
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  • 12. Aspartylglycosaminuria (AGU). Further aspects on its clinical picture, mode of inheritance and epidemiology based on a series of 57 patients.
    Autio S, Visakorpi JK, Järvinen H.
    Ann Clin Res; 1973 Jun; 5(3):149-55. PubMed ID: 4356121
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  • 15. Aspartylglycosaminuria in an Italian family: clinical and biochemical characteristics.
    Gehler J, Sewell AC, Becker C, Spranger J, Hartmann J.
    J Inherit Metab Dis; 1981 Jun; 4(4):229-30. PubMed ID: 6796777
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  • 16. Quantitative determination of 4-N-2-acetamido-2-deoxy-beta-D-glucopyranosyl-L-asparagine in the urine of patients with aspartylglycosaminuria by gas-liquid chromatography.
    Maury P.
    J Lab Clin Med; 1979 May; 93(5):718-23. PubMed ID: 429870
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  • 18. The relationship between proline and hydroxyproline urinary excretion in human as an index of collagen catabolism.
    Nusgens B, Lapiere CM.
    Clin Chim Acta; 1973 Oct 12; 48(2):203-11. PubMed ID: 4758883
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  • 19. The urinary excretion of hydroxyproline in metabolic disorders of connective tissue and bone.
    Birkenhäger JC.
    Folia Med Neerl; 1970 Oct 12; 13(2):79-87. PubMed ID: 5422995
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