A method for the rapid detection of urinary glycopeptides in α-N-acetylgalactosaminidase deficiency and other lysosomal storage diseases
- 1 September 1990
- journal article
- research article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 190 (1-2) , 81-91
- https://doi.org/10.1016/0009-8981(90)90282-w
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Neuroaxonal Dystrophy Due to Lysosomal α-N-Acetylgalactosaminidase DeficiencyNew England Journal of Medicine, 1989
- NOVEL LYSOSOMAL GLYCOAMINOACID STORAGE DISEASE WITH ANGIOKERATOMA CORPORIS DIFFUSUMThe Lancet, 1989
- Isolation and Structural Characterization of Sialic Acid-Containing Glycopeptides of the O-GlycosidicType from the Urine of Two Patients with an Hereditary Deliciency in α-N-Acetylgalactosaminidase ActivityBiological Chemistry Hoppe-Seyler, 1989
- LYSOSOMAL α-N-ACETYLGALACTOSAMINIDASE DEFICIENCY: A NEW INHERITED METABOLIC DISEASEThe Lancet, 1987
- Human β-Mannosidase DeficiencyNew England Journal of Medicine, 1986
- Thin-layer chromatography of oligosaccharides in urine as a rapid indication for the diagnosis of lysosomal acid maltase deficiency (Pompe's disease)Clinica Chimica Acta; International Journal of Clinical Chemistry, 1983
- Urinary oligosaccharide excretion in disorders of glycolipid, glycoprotein and glycogen metabolismEuropean Journal of Pediatrics, 1980
- Oligosaccharides in urine of patients with glycoprotein storage diseases: I. Rapid detection by thin-layer chromatographyClinica Chimica Acta; International Journal of Clinical Chemistry, 1975
- Structures and serological activities of three oligosaccharides isolated from urines of nonstarved secretors and from secretors on lactose dietBiochemistry, 1973
- Studies on serum and urinary glycopeptides and glycosaminoglycans in aspartylglucosaminuriaClinica Chimica Acta; International Journal of Clinical Chemistry, 1972