Diagnosis of genetic mucopolysaccharidoses: Electrophoretic and enzymatic characterization of urinary glycosaminoglycans
- 1 November 1975
- journal article
- research article
- Published by Elsevier in Biochemical Medicine
- Vol. 14 (3) , 241-249
- https://doi.org/10.1016/0006-2944(75)90042-3
Abstract
No abstract availableKeywords
Funding Information
- Ministry of Education
This publication has 21 references indexed in Scilit:
- Molecular size difference of urinary heparan sulfates from normal individuals and genetic mucopoly-saccharidosesClinica Chimica Acta; International Journal of Clinical Chemistry, 1975
- Sanfilippo A Syndrome SULFAMIDASE DEFICIENCY IN CULTURED SKIN FIBROBLASTS AND LIVERJournal of Clinical Investigation, 1974
- Characterization of glycosaminoglycans in rabbit plasma and leukocytes at disaccharide subunit levelBiochimica et Biophysica Acta (BBA) - General Subjects, 1974
- Differentiation of Hunter's and Hurler's syndromes by the analysis of the excreted mucopolysaccharidesBiochemical Medicine, 1973
- Hunter's syndrome: A deficiency of L-idurono-sulfate sulfataseBiochemical and Biophysical Research Communications, 1973
- The Sanfilippo B corrective factor: A N-acetyl-α-D-glucosaminidaseBiochemical and Biophysical Research Communications, 1972
- Hurler's syndrome, an a-L-iduronidase deficiencyBiochemical and Biophysical Research Communications, 1972
- Increased urinary excretion of chondroitin sulfate A and C in Hunter's syndromeBiochimica et Biophysica Acta (BBA) - General Subjects, 1970
- Diagnosis of Hurler's syndrome in the hospital laboratory and the determination of its genetic type.Archives of Disease in Childhood, 1966
- Mental retardation associated with acid mucopolysacchariduria (heparitin sulfate type)The Journal of Pediatrics, 1963