170 related articles for article (PubMed ID: 4742222)
1. 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]
2. Hexosaminidase A in tears and saliva for rapid identification of Tay-Sachs disease and its carriers.
Singer JD; Cotlier E; Krimmer R
Lancet; 1973 Nov; 2(7838):116-9. PubMed ID: 4128049
[No Abstract] [Full Text] [Related]
3. 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]
4. 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]
5. Tay-Sachs disease: an improved, fully-automated method for heterozygote identification by tear beta-hexosaminidase assay.
Goldberg JD; Truex JH; Desnick RJ
Clin Chim Acta; 1977 May; 77(1):43-52. PubMed ID: 872421
[No Abstract] [Full Text] [Related]
6. Diagnosis of homozygotes and heterozygotes of GM2 gangliosidosis by hexoaminidases assay.
Harteman P; Paternotte P; Vagner F; Nabet P; Paysant P
Biomedicine; 1974 May; 20(3):242-8. PubMed ID: 4433658
[No Abstract] [Full Text] [Related]
7. Letter: Testing for Tay-Sachs heterozygotes.
Edwards JH
Lancet; 1973 Nov; 2(7838):1143-4. PubMed ID: 4128027
[No Abstract] [Full Text] [Related]
8. A screening program for Tay-Sachs disease in Israel.
Padeh B
Isr J Med Sci; 1973; 9(9):1330-4. PubMed ID: 4775113
[No Abstract] [Full Text] [Related]
9. Tay-sachs disease. Detection of heterozygotes and homozygotes by serum hexosaminidase assay.
O'Brien JS; Okada S; Chen A; Fillerup DL
N Engl J Med; 1970 Jul; 283(1):15-20. PubMed ID: 4986776
[No Abstract] [Full Text] [Related]
10. [Detection of carriers of Tay-Sachs disease by determining blood N-acetylhexosaminadase A activity].
Tsvetkova IV; Kozina AB
Vopr Med Khim; 1974; 20(6):631-4. PubMed ID: 4450529
[No Abstract] [Full Text] [Related]
11. Tay-Sachs disease in a Moroccan Jewish family: a possible new mutation.
Bach G; Navon R; Zeigler M; Beyth Y; Porter B; Cohen MM
Isr J Med Sci; 1976 Dec; 12(12):1432-9. PubMed ID: 1017941
[TBL] [Abstract][Full Text] [Related]
12. Determination of Tay-Sachs genotypes in pregnant women.
Navon R; Mark Z; Mashiah S; Padeh B
Clin Genet; 1973; 4(3):286-7. PubMed ID: 4765212
[No Abstract] [Full Text] [Related]
13. Automated determination of serum hexosaminidase A by pH inactivation for detection of Tay-Sachs disease heterozygotes.
Saifer A; Perle G
Clin Chem; 1974 May; 20(5):538-43. PubMed ID: 4826945
[No Abstract] [Full Text] [Related]
14. Absence of hexosaminidase A and B in a normal adult.
Dreyfus JC; Poenaru L; Svennerholm L
N Engl J Med; 1975 Jan; 292(2):61-3. PubMed ID: 1109441
[TBL] [Abstract][Full Text] [Related]
15. Tay-Sachs carrier detection by mechanized serum hexosaminidase assay.
Rosenberg D; Cutler R
Clin Chim Acta; 1974 Jun; 53(2):247-53. PubMed ID: 4841990
[No Abstract] [Full Text] [Related]
16. Tay-Sachs disease heterozygote detection: a quality control study.
Kaback MM; Shapiro LJ; Hirsch P; Roy C
Prog Clin Biol Res; 1977; 18():267-79. PubMed ID: 601080
[No Abstract] [Full Text] [Related]
17. Separation of N-acetyl- -D-hexosaminamidase-isoenzymes from human brain and leukocytes by cellulose acetate paper electrophoresis: a simple procedure for the diagnosis of Tay-Sachs disease.
Klibansky C
Isr J Med Sci; 1971 Sep; 7(9):1086-9. PubMed ID: 5151274
[No Abstract] [Full Text] [Related]
18. Caveats of antenatal diagnosis of Tay-Sachs disease.
Saifer A; Schneck L; Perle G; Valenti C; Volk BW
Am J Obstet Gynecol; 1973 Feb; 115(4):554-5. PubMed ID: 4685506
[No Abstract] [Full Text] [Related]
19. [Prenatal genetic diagnosis in a family with Tay-Sachs disease (enzyme variant B) (author's transl)].
Pilz H; Linke I; Käckell MY; Haller J; Lenard HG
Dtsch Med Wochenschr; 1974 Mar; 99(12):578-80. PubMed ID: 4835528
[No Abstract] [Full Text] [Related]
20. [Prenatal biochemical diagnosis of Tay-Sachs disease].
Rozenfel'd EL; Tsvetkova IV; Kozina AB; Rozovskiĭ IS; Kovrigina NG
Vopr Med Khim; 1972; 18(4):445-6. PubMed ID: 4661856
[No Abstract] [Full Text] [Related]
[Next] [New Search]
