These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
122 related articles for article (PubMed ID: 4884797)
1. Acid hydrolases in plasma in Gaucher's disease. Ockerman PA; Kohlin P Clin Chem; 1969 Jan; 15(1):61-4. PubMed ID: 4884797 [No Abstract] [Full Text] [Related]
2. Lysosomal enzyme activities in platelets of normal individuals and of patients with Gaucher's disease. Yatziv S; White M; Eldor A Thromb Diath Haemorrh; 1974 Dec; 32(2-3):665-9. PubMed ID: 4450208 [No Abstract] [Full Text] [Related]
4. Influence of age and sex on plasma acid hydrolases. Eriksson O; Ginsburg BE; Hultberg B; Ockerman PA Clin Chim Acta; 1972 Aug; 40(1):181-5. PubMed ID: 5056627 [No Abstract] [Full Text] [Related]
5. Acid hydrolases in serum from patients with lysosomal disorders. Hultberg B; Isaksson A; Sjöblad S; Ockerman PA Clin Chim Acta; 1980 Jan; 100(1):33-8. PubMed ID: 6766092 [TBL] [Abstract][Full Text] [Related]
6. Acid hydrolases in leukocytes and platelets of normal subjects and in patients with Gaucher's and Fabry's disease. Beutler E; Kuhl W; Matsumoto F; Pangalis G J Exp Med; 1976 Apr; 143(4):975-80. PubMed ID: 3620 [TBL] [Abstract][Full Text] [Related]
7. The nature of disaccharidases in human leukocytes. Hsia DY; Monteleleone J; Farquhar J J Lab Clin Med; 1969 Jan; 73(1):111-20. PubMed ID: 4302789 [No Abstract] [Full Text] [Related]
9. Acid hydrolases in skin and plasma in gargoylism. Deficiency of beta-galactosidase in skin. Ockerman PA Clin Chim Acta; 1968 Apr; 20(1):1-6. PubMed ID: 4967992 [No Abstract] [Full Text] [Related]
10. 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]
11. Characterization of lysosomal hydrolases that are elevated in Gaucher's disease. Moffitt KD; Chambers JP; Diven WF; Glew RH; Wenger DA; Farrell DF Arch Biochem Biophys; 1978 Sep; 190(1):247-60. PubMed ID: 101149 [No Abstract] [Full Text] [Related]
16. Pseudo-Hurler polydystrophy (mucolipidosis 3). A clinical, biochemical and ultrastructural study. Stein H; Berman ER; Livni N; Merin S; Sheskin J; Cohen T Isr J Med Sci; 1974 May; 10(5):463-75. PubMed ID: 4213328 [No Abstract] [Full Text] [Related]
17. 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]
18. The use of white cells as a source of diagnostic material for lipid storage diseases. Snyder RA; Brady RO Clin Chim Acta; 1969 Aug; 25(2):331-8. PubMed ID: 4895581 [No Abstract] [Full Text] [Related]
19. Demonstration of a deficiency of beta-xylosidase activity in various forms of Gaucher's disease. Chiao YB; Peters SP; Diven WF; Lee RE; Glew RH Metabolism; 1979 Jan; 28(1):56-62. PubMed ID: 759826 [No Abstract] [Full Text] [Related]
20. Plasma acid hydrolases in normal adults and children, and in patients with some lysosomal storage diseases. Griffiths PA; Milsom JP; Lloyd JB Clin Chim Acta; 1978 Dec; 90(2):129-41. PubMed ID: 31250 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]