These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

100 related items for PubMed ID: 992027

  • 1. 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
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. Aspartylglycosaminuria in an Italian family: clinical and biochemical characteristics.
    Gehler J, Sewell AC, Becker C, Spranger J, Hartmann J.
    J Inherit Metab Dis; 1981 Oct 15; 4(4):229-30. PubMed ID: 6796777
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. N-Acetylglucosamine-asparagine levels in tissues of patients with aspartylglycosaminuria.
    Maury CP, Palo J.
    Clin Chim Acta; 1980 Dec 08; 108(2):293-9. PubMed ID: 7449147
    [Abstract] [Full Text] [Related]

  • 6. Accumulation of glycoprotein-derived metabolites in neural and visceral tissue in aspartylglycosaminuria.
    Maury CP.
    J Lab Clin Med; 1980 Nov 08; 96(5):838-44. PubMed ID: 7419967
    [Abstract] [Full Text] [Related]

  • 7. Aspartylglucosamine excretion in heterozygous carriers of aspartylglycosaminuria.
    Mononen TK.
    Clin Chim Acta; 1989 Mar 15; 180(1):99-101. PubMed ID: 2743573
    [No Abstract] [Full Text] [Related]

  • 8. Characterization of the storage material of peripheral lymphocytes in aspartylglycosaminuria.
    Maury P, Palo J.
    Clin Sci (Lond); 1980 Feb 15; 58(2):165-8. PubMed ID: 7357836
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Prenatal diagnosis and fetal pathology of aspartylglucosaminuria.
    Aula P, Rapola J, von Koskull H, Ammälä P.
    Am J Med Genet; 1984 Oct 15; 19(2):359-67. PubMed ID: 6507482
    [Abstract] [Full Text] [Related]

  • 12. Liquid-chromatographic detection of aspartylglycosaminuria.
    Mononen T, Parviainen M, Penttilä I, Mononen I.
    Clin Chem; 1986 Mar 15; 32(3):501-2. PubMed ID: 3948393
    [Abstract] [Full Text] [Related]

  • 13. Structural studies of glycoasparagines from urine of a patient with aspartylglycosylaminuria (AGU).
    Sugahara K, Akasaki M, Funakoshi I, Aula P, Yamashina I.
    FEBS Lett; 1977 Jun 15; 78(2):284-6. PubMed ID: 885252
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. 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 Jun 15; 36(2):179-89. PubMed ID: 6788730
    [Abstract] [Full Text] [Related]

  • 19. 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
    [Abstract] [Full Text] [Related]

  • 20. Extra heating of TLC plates detects two lysosomal storage diseases, aspartylglucosaminuria and fucosidosis, during routine urinary amino acid screening.
    Simell O, Sipilä I, Autio S.
    Clin Chim Acta; 1983 Sep 30; 133(2):227-32. PubMed ID: 6627685
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 5.