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22. Serum beta-hexosaminidases in pregnancy. Lowden JA Clin Chim Acta; 1979 May; 93(3):409-17. PubMed ID: 445857 [TBL] [Abstract][Full Text] [Related]
23. Prenatal diagnosis of Tay-Sachs disease with heat-labile beta-hexosaminidase B. Momoi T; Kikuchi K; Shigematsu Y; Sudo M; Tanioka K Clin Chim Acta; 1983 Oct; 133(3):331-4. PubMed ID: 6226459 [TBL] [Abstract][Full Text] [Related]
24. [Reconstruction of hexosaminidase isoenzymes during hybridization of fibroblasts from Tay-Sachs and Sandhoff diseases]. Beĭer EM; Vidershaĭn GIa; Venert M Biull Eksp Biol Med; 1984 Jan; 97(1):83-6. PubMed ID: 6229294 [TBL] [Abstract][Full Text] [Related]
25. Increase of intermediate forms of beta-N-acetylhexosaminidase during rat liver development and regeneration. Emiliani C; Locci P; Becchetti E; Marinucci L; Bellachioma G; Orlacchio A Int J Biochem; 1991; 23(2):215-9. PubMed ID: 1825639 [TBL] [Abstract][Full Text] [Related]
26. Electrophoresis with direct fluorometry for the diagnosis of Tay-Sachs disease and carriers. Saruwatari AS; Schmidt BJ; Diament AJ Clin Chem; 1986 Jun; 32(6):1232-3. PubMed ID: 2940030 [No Abstract] [Full Text] [Related]
27. In situ assessment of beta-hexosaminidase activity. Lacorazza HD; Jendoubi M Biotechniques; 1995 Sep; 19(3):434-40. PubMed ID: 7495557 [TBL] [Abstract][Full Text] [Related]
28. Tay-Sachs and Sandhoff diseases: enzymatic diagnosis in dried blood spots on filter paper: retrospective diagnoses in newborn-screening cards. Chamoles NA; Blanco M; Gaggioli D; Casentini C Clin Chim Acta; 2002 Apr; 318(1-2):133-7. PubMed ID: 11880123 [TBL] [Abstract][Full Text] [Related]
29. Screening for carriers of Tay-Sachs disease among Ashkenazi Jews. A comparison of DNA-based and enzyme-based tests. Triggs-Raine BL; Feigenbaum AS; Natowicz M; Skomorowski MA; Schuster SM; Clarke JT; Mahuran DJ; Kolodny EH; Gravel RA N Engl J Med; 1990 Jul; 323(1):6-12. PubMed ID: 2355960 [TBL] [Abstract][Full Text] [Related]
30. Splice junction mutation in some Ashkenazi Jews with Tay-Sachs disease: evidence against a single defect within this ethnic group. Myerowitz R Proc Natl Acad Sci U S A; 1988 Jun; 85(11):3955-9. PubMed ID: 3375249 [TBL] [Abstract][Full Text] [Related]
31. Adult GM2 gangliosidosis in association with Tay-Sachs disease: a new phenotype. Navon R; Argov Z; Brand N; Sandbank U Neurology; 1981 Nov; 31(11):1397-1401. PubMed ID: 6458776 [No Abstract] [Full Text] [Related]
32. Maternal serum hexosaminidase A in pregnancy: effects of gestational age and fetal genotype. Ben-Yoseph Y; Pack BA; Thomas PM; Nadler HL; Kaback MM Am J Med Genet; 1988 Apr; 29(4):891-9. PubMed ID: 2969680 [TBL] [Abstract][Full Text] [Related]
33. Tay-Sachs disease with altered beta-hexosaminidase B: a new variant? Momoi T; Sudo M; Tanioka K; Nakao Y Pediatr Res; 1978 Feb; 12(2):77-81. PubMed ID: 25409 [No Abstract] [Full Text] [Related]
34. 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]
35. Assay of serum/plasma beta-N-acetylhexosaminidase isoenzymes by heat inactivation using a continuous spectrophotometric method adapted to a centrifugal analyzer. Pérez LF; Tutor JC Eur J Clin Chem Clin Biochem; 1997 Jun; 35(6):445-52. PubMed ID: 9228328 [TBL] [Abstract][Full Text] [Related]