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2. Enzyme patterns in tissues and body fluids in mucopolysaccharidoses. Ockerman PA; Hultberg B; Eriksson O Clin Chim Acta; 1969 Jul; 25(1):97-102. PubMed ID: 4240390 [No Abstract] [Full Text] [Related]
3. -Galactosidase, N-acetyl- -glucosaminidase, and -glucuronidase activity in fibroblast cultures from patients with mucopolysaccharide storage disease. Lagunoff D; Pritzl P; Scott CR Biochem Med; 1973 Jun; 7(3):343-9. PubMed ID: 4268484 [No Abstract] [Full Text] [Related]
4. Sanfilippo syndrome: profound deficiency of alpha-acetylglucosaminidase activity in organs and skin fibroblasts from type-B patients. O'Brien JS Proc Natl Acad Sci U S A; 1972 Jul; 69(7):1720-2. PubMed ID: 4261742 [TBL] [Abstract][Full Text] [Related]
5. Lysosomal enzymes of cultured fibroblasts of cystic fibrosis patients. Butterworth J; Scott F; McCrae WM; Bain AD Clin Chim Acta; 1972 Aug; 40(1):139-42. PubMed ID: 4262514 [No Abstract] [Full Text] [Related]
6. Acid hydrolases in the serum and liver in mucopolysaccharidoses types I and 3. Gordon BA; Feleki V Clin Biochem; 1970 Sep; 3(3):193-202. PubMed ID: 4258597 [No Abstract] [Full Text] [Related]
12. A recognition marker required for uptake of a lysosomal enzyme by cultured fibroblasts. Hickman S; Shapiro LJ; Neufeld EF Biochem Biophys Res Commun; 1974 Mar; 57(1):55-61. PubMed ID: 4364008 [No Abstract] [Full Text] [Related]
13. N-acetyl-beta-hexosaminidase: role in the degradation of glycosaminoglycans. Thompson JN; Stoolmiller AC; Matalon R; Dorfman A Science; 1973 Aug; 181(4102):866-7. PubMed ID: 4269276 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Arylsulfatase B deficiency in Maroteaux-Lamy syndrome cultured fibroblasts. Fluharty AL; Stevens RL; Sanders DL; Kihara H Biochem Biophys Res Commun; 1974 Jul; 59(2):455-61. PubMed ID: 4277366 [No Abstract] [Full Text] [Related]
17. Hurler's syndrome, an -L-iduronidase deficiency. Matalon R; Dorfman A Biochem Biophys Res Commun; 1972 May; 47(4):959-64. PubMed ID: 4260316 [No Abstract] [Full Text] [Related]
18. Abnormal arylsulphatase activities of fibroblasts cultured from patients with mucopolysaccharidosis and cystinosis. Furusho K; Vetrella M; Latta E Z Kinderheilkd; 1971; 110(4):324-31. PubMed ID: 4254863 [No Abstract] [Full Text] [Related]
19. [Biochemical heterogeneity of Sanfilippos' disease (mucopolysaccharidosis 3). Purification and enzymatic activity of one of the missing proteins]. Kresse H Hoppe Seylers Z Physiol Chem; 1972 May; 353(5):728-9. PubMed ID: 4262625 [No Abstract] [Full Text] [Related]
20. [Increase of the serum activity of hyaluronidase, beta glucuronidase and beta acetylglucosaminidase in mucopolysaccharidoses]. Platt D; Koch F Klin Wochenschr; 1969 Aug; 47(16):888-9. PubMed ID: 4245626 [No Abstract] [Full Text] [Related] [Next] [New Search]