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Journal Abstract Search

117 related items for PubMed ID: 723900

  • 21. 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; 16(4):367-76. PubMed ID: 3132350
    [Abstract] [Full Text] [Related]

  • 22. High prevalence of aspartylglycosaminuria among school-age children in eastern Finland.
    Mononen T, Mononen I, Matilainen R, Airaksinen E.
    Hum Genet; 1991 Jul; 87(3):266-8. PubMed ID: 1864600
    [Abstract] [Full Text] [Related]

  • 23. Aspartylglucosaminuria, clinical aspects.
    Autio S, Palo J, Visakorpi JK, Iivanainen M.
    Acta Paediatr Scand Suppl; 1970 Jul; 206():Suppl 206:70+. PubMed ID: 5280254
    [No Abstract] [Full Text] [Related]

  • 24. Laboratory detection of aspartylglycosaminuria.
    Mononen I, Kaartinen V, Mononen T.
    Scand J Clin Lab Invest Suppl; 1988 Jul; 191():7-11. PubMed ID: 3247584
    [Abstract] [Full Text] [Related]

  • 25. Studies on serum and urinary glycopeptides and glycosaminoglycans in aspartylglucosaminuria.
    Palo J, Savolainen H.
    Clin Chim Acta; 1972 Feb; 36(2):431-7. PubMed ID: 4257761
    [No Abstract] [Full Text] [Related]

  • 26. Screening test for aspartylglycosaminuria.
    Humbel R, Marchal C.
    J Pediatr; 1974 Mar; 84(3):456. PubMed ID: 4811998
    [No Abstract] [Full Text] [Related]

  • 27. Amniotic fluid glycoasparagines in fetal aspartylglycosaminuria.
    Mononen I, Kaartinen V, Mononen T.
    J Inherit Metab Dis; 1988 Mar; 11(2):194-8. PubMed ID: 3139932
    [Abstract] [Full Text] [Related]

  • 28. Letter: Aspartylglycosaminuria in Northern Norway.
    Borud O, Torp KH.
    Lancet; 1976 May 15; 1(7968):1082-3. PubMed ID: 57494
    [No Abstract] [Full Text] [Related]

  • 29. Characterization of two glycoasparagines isolated from the urine of patients with aspartylglycosylaminuria (AGU).
    Sugahara K, Funakoshi S, Funakoshi I, Aula P, Yamashina I.
    J Biochem; 1975 Oct 15; 78(4):673-8. PubMed ID: 1213985
    [Abstract] [Full Text] [Related]

  • 30. [Aspartylglucosaminuria. A hereditary disease with unusual high incidence among Finns in northern Norway].
    Torp KH, Borud O.
    Tidsskr Nor Laegeforen; 1978 Aug 30; 98(24):1145-6. PubMed ID: 684720
    [No Abstract] [Full Text] [Related]

  • 31. The genetic mucolipidoses--definition and classification.
    Spranger J.
    Birth Defects Orig Artic Ser; 1975 Aug 30; 11(6):251-6. PubMed ID: 811278
    [No Abstract] [Full Text] [Related]

  • 32. Disturbed metabolism of copper and zinc in aspartylglycosaminuria: possible involvement with connective tissue changes.
    Näntö-Salonen K, Halme T, Penttinen R, Langevelde FV, Vis RD, Alfthan G.
    J Inherit Metab Dis; 1985 Aug 30; 8(4):212-8. PubMed ID: 3939546
    [Abstract] [Full Text] [Related]

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  • 37. Letter: Leukocyte function in aspartylglucosaminuria.
    Fleisher TA, Isenberg JN, Sharp HL.
    J Pediatr; 1975 Nov 30; 87(5):833. PubMed ID: 1185361
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