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Journal Abstract Search

173 related items for PubMed ID: 1777981

  • 1. Urinary oligosaccharide excretion and severity of galactosialidosis and sialidosis.
    Takahashi Y, Nakamura Y, Yamaguchi S, Orii T.
    Clin Chim Acta; 1991 Dec 16; 203(2-3):199-210. PubMed ID: 1777981
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  • 2. A comparative study of sialyloligosaccharides isolated from sialidosis and galactosialidosis urine.
    Van Pelt J, Kamerling JP, Bakker HD, Vliegenthart JF.
    J Inherit Metab Dis; 1991 Dec 16; 14(5):730-40. PubMed ID: 1779619
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  • 3. Severe infantile sialidosis--the characteristics of oligosaccharides isolated from the urine and the abdominal ascites.
    Nakamura Y, Takahashi Y, Yamaguchi S, Omiya S, Orii T, Yara A, Gushiken M.
    Tohoku J Exp Med; 1992 Apr 16; 166(4):407-15. PubMed ID: 1502687
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  • 4. Urinary oligosaccharide excretion in nephrotic syndrome.
    Takahashi Y, Omiya S, Nakamura Y, Kondo N, Orii T.
    Pediatr Res; 1993 Oct 16; 34(4):429-34. PubMed ID: 8255672
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  • 5. Glycan profiling of urine, amniotic fluid and ascitic fluid from galactosialidosis patients reveals novel oligosaccharides with reducing end hexose and aldohexonic acid residues.
    Bruggink C, Poorthuis BJ, Piraud M, Froissart R, Deelder AM, Wuhrer M.
    FEBS J; 2010 Jul 16; 277(14):2970-86. PubMed ID: 20546307
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  • 6. Severity of GM1 gangliosidosis and urinary oligosaccharide excretion.
    Takahashi Y, Orii T.
    Clin Chim Acta; 1989 Feb 15; 179(2):153-62. PubMed ID: 2493350
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  • 7. Application of a protocol for the detection of disorders of sialic acid metabolism to 124 high-risk Brazilian patients.
    Castilhos CD, Mello AS, Burin MG, Guidobono RR, Gotardo S, Giugliani R, Coelho JC.
    Am J Med Genet A; 2003 Jun 15; 119A(3):348-51. PubMed ID: 12784303
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  • 8. Oligosaccharide analysis in urine by maldi-tof mass spectrometry for the diagnosis of lysosomal storage diseases.
    Xia B, Asif G, Arthur L, Pervaiz MA, Li X, Liu R, Cummings RD, He M.
    Clin Chem; 2013 Sep 15; 59(9):1357-68. PubMed ID: 23676310
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  • 9. [Thin-layer chromatography of urine oligosaccharides in diagnosis of some lysosomal storage disorders].
    Lugowska A, Tylki-Szymańska A, Sawnor-Korszyńska D.
    Pediatr Pol; 1995 Oct 15; 70(10):847-55. PubMed ID: 8649932
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  • 16. Development of a new tandem mass spectrometry method for urine and amniotic fluid screening of oligosaccharidoses.
    Piraud M, Pettazzoni M, Menegaut L, Caillaud C, Nadjar Y, Vianey-Saban C, Froissart R.
    Rapid Commun Mass Spectrom; 2017 Jun 15; 31(11):951-963. PubMed ID: 28370531
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  • 17. [Genetic advances in galactosialidosis].
    Hirasawa M.
    Nihon Rinsho; 1993 Sep 15; 51(9):2319-23. PubMed ID: 8411708
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  • 18. Storage of sialic acid-containing carbohydrates in the placenta of a human galactosialidosis fetus. Isolation and structural characterization of 16 sialyloligosaccharides.
    Van Pelt J, Van Kuik JA, Kamerling JP, Vliegenthart JF, Van Diggelen OP, Galjaard H.
    Eur J Biochem; 1988 Nov 01; 177(2):327-38. PubMed ID: 3142773
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  • 19. Juvenile galactosialidosis with attacks of neuropathic pain and absence of sialyloligosacchariduria.
    Darin N, Kyllerman M, Hård AL, Nordborg C, Månsson JE.
    Eur J Paediatr Neurol; 2009 Nov 01; 13(6):553-5. PubMed ID: 19097920
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