These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 4128049)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Urinary hexosaminidase analysis for the identification of Tay-Sachs genotypes.
    Saifer A; Amoroso J; Perle G
    Clin Chim Acta; 1976 Mar; 67(3):315-9. PubMed ID: 4244
    [No Abstract]   [Full Text] [Related]  

  • 9. Hair-roots in screening and diagnosis of Tay-Sachs disease.
    Hösli P; Amsterdam D; Schneck L; Volk BW
    Lancet; 1977 Feb; 1(8006):285-7. PubMed ID: 64809
    [No Abstract]   [Full Text] [Related]  

  • 10. 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]  

  • 11. Kinetic determination of hexosaminidases for Tay-Sachs heterozygote screening.
    Zinterhofer L; Schuttringer G
    Clin Chem; 1976 Oct; 22(10):1631-4. PubMed ID: 975509
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. [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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 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. 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]  

  • 20. Editorial: Heterozygote screening--a social challenge.
    Kaback MM
    N Engl J Med; 1973 Nov; 289(20):1090-1. PubMed ID: 4742226
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.