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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; 277(14):2970-86. PubMed ID: 20546307 [TBL] [Abstract][Full Text] [Related]
6. Severity of GM1 gangliosidosis and urinary oligosaccharide excretion. Takahashi Y; Orii T Clin Chim Acta; 1989 Feb; 179(2):153-62. PubMed ID: 2493350 [TBL] [Abstract][Full Text] [Related]
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; 119A(3):348-51. PubMed ID: 12784303 [TBL] [Abstract][Full Text] [Related]
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; 59(9):1357-68. PubMed ID: 23676310 [TBL] [Abstract][Full Text] [Related]
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; 70(10):847-55. PubMed ID: 8649932 [TBL] [Abstract][Full Text] [Related]
10. UPLC-MS/MS Analysis of Urinary Free Oligosaccharides for Lysosomal Storage Diseases: Diagnosis and Potential Treatment Monitoring. Huang R; Cathey S; Pollard L; Wood T Clin Chem; 2018 Dec; 64(12):1772-1779. PubMed ID: 30201803 [TBL] [Abstract][Full Text] [Related]
11. A comparative study of the accumulated sialic acid-containing oligosaccharides from cultured human galactosialidosis and sialidosis fibroblasts. van Pelt J; Kamerling JP; Vliegenthart JF; Hoogeveen AT; Galjaard H Clin Chim Acta; 1988 Jun; 174(3):325-35. PubMed ID: 3134148 [TBL] [Abstract][Full Text] [Related]
12. The biochemistry and clinical features of galactosialidosis. Okamura-Oho Y; Zhang S; Callahan JW Biochim Biophys Acta; 1994 Feb; 1225(3):244-54. PubMed ID: 8312369 [TBL] [Abstract][Full Text] [Related]
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; 31(11):951-963. PubMed ID: 28370531 [TBL] [Abstract][Full Text] [Related]
17. [Genetic advances in galactosialidosis]. Hirasawa M Nihon Rinsho; 1993 Sep; 51(9):2319-23. PubMed ID: 8411708 [TBL] [Abstract][Full Text] [Related]
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; 177(2):327-38. PubMed ID: 3142773 [TBL] [Abstract][Full Text] [Related]
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; 13(6):553-5. PubMed ID: 19097920 [TBL] [Abstract][Full Text] [Related]
20. The presence of a reduced amount of 32-kd "protective" protein is a distinct biochemical finding in late infantile galactosialidosis. Strisciuglio P; Parenti G; Giudice C; Lijoi S; Hoogeveen AT; d'Azzo A Hum Genet; 1988 Nov; 80(3):304-6. PubMed ID: 3142815 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]