152 related articles for article (PubMed ID: 6226459)
1. 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]
2. 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]
3. Prenatal diagnosis for Tay-Sachs disease using chorionic villus sampling.
Grebner EE; Jackson LG
Prenat Diagn; 1985; 5(5):313-20. PubMed ID: 2933645
[TBL] [Abstract][Full Text] [Related]
4. Prenatal diagnosis of Tay-Sachs disease in cell-free amniotic fluid.
Christomanou H; Cáp C; Sandhoff K
Klin Wochenschr; 1978 Nov; 56(22):1133-5. PubMed ID: 713433
[TBL] [Abstract][Full Text] [Related]
5. Hexosaminidase A in amniotic fluid of Tay-Sachs fetuses.
Geiger B; Navon R; Arnon R
Clin Chem; 1978 Jul; 24(7):1131-3. PubMed ID: 657491
[TBL] [Abstract][Full Text] [Related]
6. First-trimester prenatal diagnosis of Tay-Sachs disease.
Grabowski GA; Kruse JR; Goldberg JD; Chockkalingam K; Gordon RE; Blakemore KJ; Mahoney MJ; Desnick RJ
Am J Hum Genet; 1984 Nov; 36(6):1369-78. PubMed ID: 6240199
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of Tay-Sachs disease: studies on the reliability of hexosaminidase levels in amniotic fluid.
Grebner EE; Jackson LG
Am J Obstet Gynecol; 1979 Jul; 134(5):547-50. PubMed ID: 453293
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. The prenatal diagnosis of Tay-Sachs disease.
Lane AB; Skikne MI; Jenkins T
S Afr Med J; 1976 Sep; 50(40):1553-5. PubMed ID: 982208
[TBL] [Abstract][Full Text] [Related]
10. A modified method for prenatal diagnosis of Tay-Sachs disease in cell-free amniotic fluid.
Navon R; Wiselter J; Modan M
Monogr Hum Genet; 1978; 9():186-92. PubMed ID: 732839
[No Abstract] [Full Text] [Related]
11. Prenatal diagnosis of neurolipidoses.
Grebner EE; Jackson LG
Ann Clin Lab Sci; 1982; 12(5):381-7. PubMed ID: 6215890
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis and fetal pathology of Tay-Sachs disease.
Higami S; Nishizawa K; Omura K; Sugimoto K; Isshiki G
Tohoku J Exp Med; 1976 Apr; 118(4):323-30. PubMed ID: 936207
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
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. Use of microtechniques for the detection of lysosomal enzyme disorders: Tay-Sachs disease, Gm1-gangliosidosis and Fabry disease.
Bladon MT; Milunsky A
Clin Genet; 1978 Dec; 14(6):359-66. PubMed ID: 215359
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. [GM2 gangliosidosis diagnosis and carriers detection by fractionation of N-acetyl-beta-D-hexosaminidase by electrophoresis on cellulose acetate gel (author's transl)].
Pampols T; Girós ML; González Sastre F; Sabater J
An Esp Pediatr; 1977 Oct; 10(10):695-704. PubMed ID: 607830
[TBL] [Abstract][Full Text] [Related]
19. Diagnosis of Tay-Sachs disease by estimation of beta-N-acetylhexosaminidase activity using a radiolabeled hyaluronic acid-derived trisaccharide substrate.
Yutaka T; Kato T; Midorikawa M; Doke M; Okada S; Yabuuchi H
Clin Chim Acta; 1984 Feb; 137(2):159-68. PubMed ID: 6231138
[TBL] [Abstract][Full Text] [Related]
20. A rapid and simple microfractionation method for the analysis of hexosaminidase A and B activities in small numbers of cultured (amniotic fluid) cells.
D'Azzo A; Hoogeveen A; De Wit-Verbeek HA
Clin Chim Acta; 1978 Aug; 88(1):1-7. PubMed ID: 679481
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
