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2. 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]
3. alpha-L-fucosidase in cultured skin fibroblasts from normal subjects and fucosidosis patients. Beratis NG; Turner BM; Labadie G; Hirschhorn K Pediatr Res; 1977 Jul; 11(7):862-6. PubMed ID: 17844 [TBL] [Abstract][Full Text] [Related]
4. Absence of alpha-fucosidase activity in two sisters showing a different phenotype. Christomanou H; Beyer D Eur J Pediatr; 1983 Mar; 140(1):27-9. PubMed ID: 6873107 [TBL] [Abstract][Full Text] [Related]
6. Determination of lysosomal enzymes in saliva. Confirmation of the diagnosis of metachromatic leukodystrophy and fucosidosis by enzyme analysis. Den Tandt WR; Jaeken J Clin Chim Acta; 1979 Sep; 97(1):19-25. PubMed ID: 40713 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Glycosidases in human skin fibroblast cultures. Alpha-fucosidase, alpha-galactosidase, alpha-glucosidase, beta-mannosidase, and N-acetyl-alpha-glucosaminidase. Hultberg B; Sjöblad S; Ockerman PA Acta Paediatr Scand; 1975 Jan; 64(1):123-31. PubMed ID: 234663 [TBL] [Abstract][Full Text] [Related]
9. [Histochemical study of the skin in fucosidosis]. Crovato F; Rampini E; Tomatis C; Della Cella G; Borrone C; Durand P Pathologica; 1971; 63(925):269-73. PubMed ID: 5005493 [No Abstract] [Full Text] [Related]
11. Abnormal distribution of alpha-L-fucosidase in cystic fibrosis: increased activity in skin fibroblasts. Scanlin TF; Matacic SS; Pace M; Santer UV; Glick MC Biochem Biophys Res Commun; 1977 Dec; 79(3):869-76. PubMed ID: 597312 [No Abstract] [Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. 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]
17. Multiple forms of glycosidases in the normal and pathological states. Robinson D Enzyme; 1974; 18(1):114-35. PubMed ID: 4277585 [No Abstract] [Full Text] [Related]
18. Cultured fucosidosis fibroblasts: a simple technique demonstrating storage of tritiated-fucose labeled material. Wood S Clin Genet; 1976 Sep; 10(3):183-6. PubMed ID: 963907 [TBL] [Abstract][Full Text] [Related]
19. Metabolic correction of fucosidosis fibroblasts by human alpha-L-fucosidase. Turner BM; Turner VS; Hirschhorn K J Cell Physiol; 1979 Jan; 98(1):225-35. PubMed ID: 762198 [TBL] [Abstract][Full Text] [Related]
20. The adnormal biochemistry of inherited disorders of lipid metabolism. Brady RO Fed Proc; 1973 Jun; 32(6):1660-7. PubMed ID: 4351098 [No Abstract] [Full Text] [Related] [Next] [New Search]