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45. Diagnosis of Gaucher's disease in cultured skin fibroblasts and leucocytes. Butterworth J; Broadhead DM J Inherit Metab Dis; 1978; 1(3):111-3. PubMed ID: 116079 [TBL] [Abstract][Full Text] [Related]
46. Some aspects of the cellular biochemistry of lysosomal and related glycosidases. Touster O Mol Cell Biochem; 1973 Dec; 2(2):169-77. PubMed ID: 4594433 [No Abstract] [Full Text] [Related]
47. Letter: Intestinal biopsy in lysosomal storage disease. Den Tandt WR; Vio PM; Eggermont E Lancet; 1974 Nov; 2(7889):1149. PubMed ID: 4139453 [No Abstract] [Full Text] [Related]
48. Multiple forms of acid phosphatase activity in Gaucher's disease. Chambers JP; Peters SP; Glew RH; Lee RE; McCafferty LR; Mercer DW; Wenger DA Metabolism; 1978 Jul; 27(7):801-14. PubMed ID: 26832 [TBL] [Abstract][Full Text] [Related]
49. Cell-specific differences in membrane beta-glucosidase from normal and Gaucher cells. Turner BM; Beratis NG; Hirschhorn K Biochim Biophys Acta; 1977 Feb; 480(2):442-9. PubMed ID: 13844 [TBL] [Abstract][Full Text] [Related]
50. The diagnosis of the adult type of Gaucher's disease and its carrier state by demonstration of deficiency of beta-glucosidase activity in peripheral blood leukocytes. Beutler E; Kuhl W J Lab Clin Med; 1970 Nov; 76(5):747-55. PubMed ID: 5477334 [No Abstract] [Full Text] [Related]
51. The properties of alpha-galactosidase remaining in kidney and liver of patients with Fabry's disease. Kano I; Yamakawa T Chem Phys Lipids; 1974 Dec; 13(4):283-91. PubMed ID: 4217662 [No Abstract] [Full Text] [Related]
52. Lysosomal enzymes in human platelets. Leoncini G; Balestrero F; Maresca M Cell Biochem Funct; 1985 Apr; 3(2):121-5. PubMed ID: 3836017 [TBL] [Abstract][Full Text] [Related]
53. Chediak-Higashi syndrome: abnormal lysosomal enzyme levels in granulocytes of patients and family members. Tanaka T Pediatr Res; 1980 Aug; 14(8):901-4. PubMed ID: 6252536 [TBL] [Abstract][Full Text] [Related]
54. Gaucher's disease. I. Solubilization and electrophoresis of beta-glucosidase from leukocytes and cultured fibroblasts. Choy FY; Davidson RG Pediatr Res; 1978 Dec; 12(12):1115-20. PubMed ID: 106357 [No Abstract] [Full Text] [Related]
55. Comparison of N-acyl phosphatidylethanolamines with different N-acyl groups as activators of glucocerebrosidase in various forms of Gaucher's disease. Basu A; Prence E; Garrett K; Glew RH; Ellingson JS Arch Biochem Biophys; 1985 Nov; 243(1):28-34. PubMed ID: 3933429 [TBL] [Abstract][Full Text] [Related]
56. Variation in ten lysosomal hydrolase enzyme activities in inbred mouse strains. Johnson WG; Hong JL; Knights SM Biochem Genet; 1986 Dec; 24(11-12):891-909. PubMed ID: 3026305 [TBL] [Abstract][Full Text] [Related]
57. Multiple forms of membrane-bound beta-glucosidase in Gaucher's disease. Yaqoob M; Carroll M Clin Genet; 1981 Aug; 20(2):161-7. PubMed ID: 6796311 [TBL] [Abstract][Full Text] [Related]
58. [Gaucher's and Fabry's diseases: biochemical and genetic aspects]. Caillaud C; Poenaru L J Soc Biol; 2002; 196(2):135-40. PubMed ID: 12360742 [TBL] [Abstract][Full Text] [Related]
59. Effect of acid-base changes on urinary hydrolases in Fabry's disease after renal transplantation. Berty RM; Adler S; Basu A; Glew RH J Lab Clin Med; 1990 Jun; 115(6):696-703. PubMed ID: 2164077 [TBL] [Abstract][Full Text] [Related]
60. [Gene therapy of Gaucher's and Fabry's diseases: current status and prospects]. Fabrega S; Lehn P J Soc Biol; 2002; 196(2):175-81. PubMed ID: 12360746 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]