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5. Chromatographic study of serum hexosaminidase in normal and GM 2-gangliosidosis. Yabuuchi H; Sumi K; Okada S; Yutaka T Clin Chim Acta; 1974 May; 53(1):85-9. PubMed ID: 4842420 [No Abstract] [Full Text] [Related]
6. Tay-Sachs disease--the use of tears for the detection of heterozygotes. Carmody PJ; Rattazzi MC; Davidson RG N Engl J Med; 1973 Nov; 289(20):1072-4. PubMed ID: 4742222 [No Abstract] [Full Text] [Related]
7. Segregation within a family of two mutant alleles for hexosaminidase A. Kelly TE; Reynolds LW; O'Brien JS Clin Genet; 1976 May; 9(5):540-3. PubMed ID: 1269177 [TBL] [Abstract][Full Text] [Related]
8. Automated thermal fractionation of serum hexosaminidase: effects of alteration in reaction variables and implications for Tay-Sachs disease heterozygote screening. Kaback MM; Bailin G; Hirsch P; Roy C Prog Clin Biol Res; 1977; 18():197-212. PubMed ID: 23554 [No Abstract] [Full Text] [Related]
9. Rapid test for the detection of Tay-Sachs disease heterozygotes and homozygotes by serum hexosaminidase assay. Saifer A; Rosenthal AL Clin Chim Acta; 1973 Feb; 43(3):417-21. PubMed ID: 4690912 [No Abstract] [Full Text] [Related]
10. Tay-Sachs disease: a pilot screening program for the detection of the heterozygote in the Charleston Jewish community. Rogers JF; Hogan EL; Jorgenson RJ South Med J; 1976 Nov; 69(11):1453-5. PubMed ID: 1019641 [TBL] [Abstract][Full Text] [Related]
11. Tay-Sachs disease: abbreviated serum hexosaminidase A test from finger-tip samples. Cotlier E Clin Chim Acta; 1972 Apr; 38(1):233-4. PubMed ID: 5031784 [No Abstract] [Full Text] [Related]
12. Automated assay of hexosaminidases in serum. Lowden JA; Skomorowski MA; Henderson F; Kaback M Clin Chem; 1973 Dec; 19(12):1345-9. PubMed ID: 4757362 [No Abstract] [Full Text] [Related]
13. A fully automated method for identification of Tay-Sachs disease carriers by tear beta-hexosaminidase assay. Desnick RJ; Truex JH; Goldberg JD Prog Clin Biol Res; 1977; 18():245-65. PubMed ID: 23556 [No Abstract] [Full Text] [Related]
14. Hexosaminidase A analysis of various biological fluids by pH inactivation for the identification of Tay-Sachs disease genotypes. Saifer A; Perle G Prog Clin Biol Res; 1977; 18():227-38. PubMed ID: 23555 [No Abstract] [Full Text] [Related]
15. Human hexosaminidase isozymes: chromatographic separation as an aid to heterozygote identification. Nakagawa S; Kumin S; Nitowsky HM Clin Chim Acta; 1977 Mar; 75(2):181-91. PubMed ID: 851488 [TBL] [Abstract][Full Text] [Related]
16. Automated differentiation and measurement of hexosaminidase isoenzymes in biological fluids and its application to pre- and postnatal detection of Tay-Sachs disease. Saifer A; Parkhurst GW; Amoroso J Clin Chem; 1975 Mar; 21(3):334-42. PubMed ID: 1112042 [TBL] [Abstract][Full Text] [Related]
17. [Enzymatic studies on the blood of carriers of a Tay-Sachs disease variant (variant O)]. Harzer K; Sandhoff K; Schall H; Kollmann F Klin Wochenschr; 1971 Nov; 49(21):1189-91. PubMed ID: 5124584 [No Abstract] [Full Text] [Related]
18. Identification of Tay-Sachs by hexosaminidase analysis of urine and tear samples. Saifer A; Amoroso J; Perle G Adv Exp Med Biol; 1976; 68():339-66. PubMed ID: 7107 [TBL] [Abstract][Full Text] [Related]