152 related articles for article (PubMed ID: 445857)
21. Prenatal diagnosis of Tay-Sachs disease. Reflectometry of hexosaminidase A, B, and C/S bands on zymograms.
Kustermann-Kuhn B; Harzer K
Hum Genet; 1983; 65(2):172-5. PubMed ID: 6228513
[TBL] [Abstract][Full Text] [Related]
22. Detection of Tay-Sachs disease carriers among individuals with thermolabile hexosaminidase B.
Peleg L; Goldman B
Eur J Clin Chem Clin Biochem; 1994 Feb; 32(2):65-9. PubMed ID: 8003579
[TBL] [Abstract][Full Text] [Related]
23. Human hexosaminidase isozymes. Assay of platelet activity for heterozygote identification during pregnancy.
Nakagawa S; Kumin S; Chandra P; Nitowsky HM
Clin Chim Acta; 1978 Sep; 88(2):249-56. PubMed ID: 699320
[TBL] [Abstract][Full Text] [Related]
24. Changes of serum hexosaminidase for the presumptive diagnosis of type I Gaucher disease in Tay-Sachs carrier screening.
Nakagawa S; Kumin S; Sachs G; Nitowsky HM
Am J Med Genet; 1983 Mar; 14(3):525-32. PubMed ID: 6859103
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. Hereditary heat-labile hexosaminidase B: its implication for recognizing Tay-Sachs genotypes.
Navon R; Nutman J; Kopel R; Gaber L; Gadoth N; Goldman B; Nitzan M
Am J Hum Genet; 1981 Nov; 33(6):907-15. PubMed ID: 6459736
[TBL] [Abstract][Full Text] [Related]
27. [Detection of homozygotes and heterozygote carriers of GM2-gangliosidosis].
Aronovich EL; Krasnopol'skaia KD; Kukharenko VI; Pichugina EM
Genetika; 1986 Aug; 22(8):2179-85. PubMed ID: 3770476
[TBL] [Abstract][Full Text] [Related]
28. Epstein-Barr virus transformed lymphoid cell lines as a new model system in culture for the study of GM2-gangliosidoses: Tay-Sachs and Sandhoff diseases.
Maret A; Salvayre R; Negre A; Bes JC; Douste-Blazy L
Biol Cell; 1985; 53(3):293-6. PubMed ID: 2990625
[TBL] [Abstract][Full Text] [Related]
29. [Genetic study of GM2 gangliosidosis (Tay-Sachs and Sandhoff) by the study of the hexosaminidases of the Sandhoff-rodents hybrids (mouse and hamster)].
Weil D; Van Cong N; Rebourcet R; Frézal J
Ann Genet; 1975 Sep; 18(3):163-8. PubMed ID: 810067
[TBL] [Abstract][Full Text] [Related]
30. Degradation of keratan sulfate by beta-N-acetylhexosaminidases in GM2-gangliosidosis.
Yutaka T; Okada S; Kato T; Yabuuhi H
Clin Genet; 1982 Mar; 21(3):196-202. PubMed ID: 6212169
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. First trimester prenatal diagnosis of Sandhoff's disease.
Giles L; Cooper A; Fowler B; Sardharwalla IB; Donnai P
Prenat Diagn; 1988 Mar; 8(3):199-205. PubMed ID: 2967473
[TBL] [Abstract][Full Text] [Related]
33. Impaired degradation of chondroitin sulfate in GM2-gangliosidosis.
Yutaka T; Kato T; Okada S; Yabuuci H
Clin Genet; 1982 Oct; 22(4):165-71. PubMed ID: 6217929
[TBL] [Abstract][Full Text] [Related]
34. The biochemical genetics of the hexosaminidase system in man.
Beutler E
Am J Hum Genet; 1979 Mar; 31(2):95-105. PubMed ID: 377957
[TBL] [Abstract][Full Text] [Related]
35. Studies in Tay-Sachs and Sandhoff's diseases. Immunologic and structural properties of hexosaminidase A and hexosaminidase B.
Beutler E; Srivastava SK
Isr J Med Sci; 1973; 9(9):1335-7. PubMed ID: 4798071
[No Abstract] [Full Text] [Related]
36. Adult-onset GM2 gangliosidosis diagnosed in a fetus.
Navon R; Sandbank U; Frisch A; Baram D; Adam A
Prenat Diagn; 1986; 6(3):169-76. PubMed ID: 2941730
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Validity of lymphoid cell line for enzymatic studies of GM2-gangliosidosis variant 0 (Sandhoff disease).
Maret A; Salvayre R; Radon J; Hardy M; Vuillaume M; Lenoir G; Douste-Blazy L
Enzyme; 1985; 34(1):48-56. PubMed ID: 3002784
[TBL] [Abstract][Full Text] [Related]
39. Inheritance of the enzyme deficiency in three neurolipidoses: variant 0 of Tay-Sachs disease (Sandhoff's disease), classic Tay-Sachs disease, and metachromatic leukodystrophy. Identification of the heterozygous carriers.
Harzer K
Humangenetik; 1973; 20(1):9-24. PubMed ID: 4776531
[No Abstract] [Full Text] [Related]
40. An altered hexosaminidase A in the liver affected by Hurler and Hunter syndromes.
Minami R; Nakamura F; Kudoh T; Oyanagi K; Nakao T
Tohoku J Exp Med; 1980 Nov; 132(3):329-35. PubMed ID: 6451055
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
