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3. Enzyme defects of glycosaminoglycan degradation in the mucopolysaccharidoses. Benson PF Dev Med Child Neurol; 1974 Aug; 16(4):534-9. PubMed ID: 4277471 [No Abstract] [Full Text] [Related]
4. The mucopolysaccharidoses: inborn errors of glycosaminoglycan catabolism. Cantz M; Gehler J Hum Genet; 1976 Jun; 32(3):233-55. PubMed ID: 820626 [TBL] [Abstract][Full Text] [Related]
5. Variation in neuronal storage in alpha-L-iduronidase deficiency. Wassman ER Am J Med Genet; 1985 Dec; 22(4):827-9. PubMed ID: 3934972 [No Abstract] [Full Text] [Related]
7. Mucopolysaccharide storage diseases and lysosomal hydrolases in cultured fibroblasts. den Tandt WR; Schaberg A Pathol Eur; 1973; 8(1):3-11. PubMed ID: 4269628 [No Abstract] [Full Text] [Related]
8. Abnormal distribution of lysosomal isoenzymes in mucopolysaccharidosis. Kint JA; Dacremont G; Carton D Arch Int Physiol Biochim; 1972 Dec; 80(5):972-3. PubMed ID: 4127090 [No Abstract] [Full Text] [Related]
9. Letter: Phenotypic variation in alpha-L-iduronidase deficiency. Leisti J; Rimoin DL; Kaback MM; Hollister DW; DEn Tandt W; Neufeld E; Matalon R; Philippart M Lancet; 1975 Jun; 1(7920):1344. PubMed ID: 49545 [No Abstract] [Full Text] [Related]
10. Absence of alpha-L-iduronidase activity in various tissues from two sibs affected with presumably the Hurler-Scheie compound syndrome. Thompson JN; Finley SC; Lorincz AE; Finley WH Birth Defects Orig Artic Ser; 1975; 11(6):341-6. PubMed ID: 811284 [No Abstract] [Full Text] [Related]
11. The abnormalities of lysosomal enzymes in mucopolysacc- haridoses. Van Hoof F; Hers HG Eur J Biochem; 1968 Dec; 7(1):34-44. PubMed ID: 4236776 [No Abstract] [Full Text] [Related]
12. Sanfilippo A syndrome (mucopolysaccharidosis III A): a neurochemical study. Federico A; Robert J; Zanetta JP; Guazzi GC Ital J Neurol Sci; 1981 May; 2(2):119-27. PubMed ID: 6800974 [No Abstract] [Full Text] [Related]
13. The Enzymatic Degradation of Heparan Sulfate. Griffin LS; Gloster TM Protein Pept Lett; 2017; 24(8):710-722. PubMed ID: 28741461 [TBL] [Abstract][Full Text] [Related]
14. Genetic complementation analysis in somatic cell hybrids of alpha-L-iduronidase deficient cells. Wehnert M; Machill G; Petruschka L Hum Genet; 1985; 69(3):287. PubMed ID: 3920140 [No Abstract] [Full Text] [Related]
15. Proceedings: Products of the breakdown of glycosaminoglycans in normal and pathological human plasma and urine. Calatroni A Ital J Biochem; 1974; 23(4):267-8. PubMed ID: 4280389 [No Abstract] [Full Text] [Related]
16. Post- and pre-natal assessment of alpha-L-iduronidase deficiency with a radiolabelled natural substrate. Hopwood JJ; Muller V; Pollard AC Clin Sci (Lond); 1979 Jan; 56(6):591-9. PubMed ID: 113163 [No Abstract] [Full Text] [Related]
17. The mucopolysaccharidoses (a review). Dorfman A; Matalon R Proc Natl Acad Sci U S A; 1976 Feb; 73(2):630-7. PubMed ID: 813230 [TBL] [Abstract][Full Text] [Related]
18. [Enzymatic diagnosis of glycolipidosis]. Zambotti V; Di Donato S; Rimoldi M; Tettamanti G Quad Sclavo Diagn; 1972 Mar; 8(1):183-98. PubMed ID: 4351703 [No Abstract] [Full Text] [Related]