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Journal Abstract Search

121 related items for PubMed ID: 7357836

  • 1. Characterization of the storage material of peripheral lymphocytes in aspartylglycosaminuria.
    Maury P, Palo J.
    Clin Sci (Lond); 1980 Feb; 58(2):165-8. PubMed ID: 7357836
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  • 3. Accumulation of glycoprotein-derived metabolites in neural and visceral tissue in aspartylglycosaminuria.
    Maury CP.
    J Lab Clin Med; 1980 Nov; 96(5):838-44. PubMed ID: 7419967
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  • 6. Clinical and biochemical delineation of aspartyl-glycosaminuria as observed in two members of an Italian family.
    Gehler J, Sewell AC, Becker C, Hartmann J, Spranger J.
    Helv Paediatr Acta; 1981 Nov; 36(2):179-89. PubMed ID: 6788730
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  • 7. Automated ion-exchange chromatography in the detection of aspartylglucosaminuria.
    Marnela KM.
    J Chromatogr; 1980 Jun 13; 182(3-4):409-13. PubMed ID: 7391183
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  • 8. 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 13; 4(4):229-30. PubMed ID: 6796777
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  • 9. Aspartylglucosamine excretion in heterozygous carriers of aspartylglycosaminuria.
    Mononen TK.
    Clin Chim Acta; 1989 Mar 15; 180(1):99-101. PubMed ID: 2743573
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  • 10. 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 Mar 15; 1(3):95-7. PubMed ID: 116085
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  • 11. Laboratory detection of aspartylglycosaminuria.
    Mononen I, Kaartinen V, Mononen T.
    Scand J Clin Lab Invest Suppl; 1988 Mar 15; 191():7-11. PubMed ID: 3247584
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  • 12. 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 Mar 15; 16(4):367-76. PubMed ID: 3132350
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  • 14. Characterization of a mannose-containing glycoasparagine isolated from urine of a patient with aspartylglycosylaminuria (AGU).
    Akasaki M, Sugahara K, Funakoshi I, Aula P, Yamashina I.
    FEBS Lett; 1976 Oct 15; 69(1):191-4. PubMed ID: 992027
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  • 15. Regional distribution of glycoasparagine storage material in the brain in aspartylglycosaminuria.
    Maury CP, Haltia M, Palo J.
    J Neurol Sci; 1981 May 15; 50(2):291-8. PubMed ID: 6164750
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  • 16. 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 May 15; 8(4):212-8. PubMed ID: 3939546
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  • 17. Identification of 4-N-2-acetamido-2-deoxy-beta-D-glucopyranosyl-L-asparagine in biological materials by gas chromatography-mass spectrometry.
    Maury P, Kärkkäinen J.
    Clin Chim Acta; 1979 Jan 01; 91(1):75-9. PubMed ID: 761395
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  • 20. Aspartylglucosaminuria in a Canadian family.
    Gordon BA, Rupar CA, Rip JW, Haust MD, Coulter-Mackie MB, Scott E, Hinton GG.
    Clin Invest Med; 1998 Jun 01; 21(3):114-23. PubMed ID: 9627765
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