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5. [Metabolic disorders of glycoproteins in congenital glycosidase deficiencies]. Yamashita K. Seikagaku; 1984 May; 56(5):285-310. PubMed ID: 6432923 [No Abstract] [Full Text] [Related]
6. Oligosaccharides in urine of patients with glycoprotein storage diseases. I. Rapid detection by thin-layer chromatography. Humbel R, Collart M. Clin Chim Acta; 1975 Apr 16; 60(2):143-5. PubMed ID: 1126036 [No Abstract] [Full Text] [Related]
7. High-performance liquid chromatographic analysis of oligosaccharides and glycopeptides accumulating in lysosomal storage disorders. Kin NM, Wolfe LS. Anal Biochem; 1980 Feb 16; 102(1):213-9. PubMed ID: 6766687 [No Abstract] [Full Text] [Related]
8. Structural studies of urinary oligosaccharides from patients with mannosidosis. Matsuura F, Nunez HA, Grabowski GA, Sweeley CC. Arch Biochem Biophys; 1981 Apr 01; 207(2):337-52. PubMed ID: 7247408 [No Abstract] [Full Text] [Related]
9. An improved thin-layer chromatographic method for urinary oligosaccharide screening. Sewell AC. Clin Chim Acta; 1979 Mar 15; 92(3):411-4. PubMed ID: 285767 [Abstract] [Full Text] [Related]
10. The catabolism of mammalian glycoproteins. Comparison of the storage products in bovine, feline and human mannosidosis. Abraham D, Blakemore WF, Jolly RD, Sidebotham R, Winchester B. Biochem J; 1983 Dec 01; 215(3):573-9. PubMed ID: 6661184 [Abstract] [Full Text] [Related]
11. Hepatic glycogenosis with defects in the glycogen breakdown pathway: urinary oligosaccharide profile. Giros ML, Alvarez L. J Inherit Metab Dis; 1991 Dec 01; 14(3):311-3. PubMed ID: 1770780 [No Abstract] [Full Text] [Related]
12. [DIFFERENTIATION OF NORM AND PATHOLOGY DURING SELECTIVE BIOCHEMICAL SKREENING OF LYSOSOMAL STORAGE DISEASES WITH INCREASED EXCRETION OF OLIGOSACCHARIDES]. Mytsyk NY, Olkhovych NV, Gorovenko NG. Ukr Biochem J; 2015 Dec 01; 87(3):107-15. PubMed ID: 26502705 [Abstract] [Full Text] [Related]
13. 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 01; 59(9):1357-68. PubMed ID: 23676310 [Abstract] [Full Text] [Related]
14. Isolation and characterization of oligosaccharides from urine of patients with abnormal glycoconjugate metabolism. Chester MA, Lennartson G, Lundblad A, Lundsten J, Nordén NE, Sjöblad S, Svensson S, Ockerman PA. Monogr Hum Genet; 1978 Sep 01; 10():2-6. PubMed ID: 102924 [No Abstract] [Full Text] [Related]
15. [Screening for oligosaccharides in the urine of infants and toddlers]. Zeman L, Zeman J, Kozich V, Bezdícková V. Cesk Pediatr; 1988 Oct 01; 43(10):590-3. PubMed ID: 3208326 [No Abstract] [Full Text] [Related]
16. Structural analysis of the major caprine beta-mannosidosis urinary oligosaccharides. Matsuura F, Jones MZ, Frazier SE. Biochim Biophys Acta; 1983 Aug 23; 759(1-2):67-73. PubMed ID: 6882792 [Abstract] [Full Text] [Related]
17. Improved thin-layer chromatographic method in the diagnosis of mannosidosis. Friedman RB, Williams MA, Moser HW, Kolodny EH. Clin Chem; 1978 Sep 23; 24(9):1576-7. PubMed ID: 688621 [Abstract] [Full Text] [Related]
18. [Oligosaccharide excretion in a case of GM 2 gangliosidosis due to total N-acetylhexosaminidase deficiency]. Strecker G, Montreuil J. Clin Chim Acta; 1971 Jul 23; 33(2):395-401. PubMed ID: 5119315 [No Abstract] [Full Text] [Related]
19. Alpha-mannosidosis: analysis of urinary oligosaccharides with high performance liquid chromatography and diagnosis of a case with unusually mild presentation. Warner TG, Mock AK, Nyhan WL, O'Brien JS. Clin Genet; 1984 Mar 23; 25(3):248-55. PubMed ID: 6705257 [Abstract] [Full Text] [Related]
20. A method for the rapid detection of urinary glycopeptides in alpha-N-acetylgalactosaminidase deficiency and other lysosomal storage diseases. Schindler D, Kanzaki T, Desnick RJ. Clin Chim Acta; 1990 Sep 23; 190(1-2):81-91. PubMed ID: 2208741 [Abstract] [Full Text] [Related] Page: [Next] [New Search]