Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 114

1.

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 2;283(1):15-20. No abstract available.

PMID:
4986776
2.
3.

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 12;43(3):417-21. No abstract available.

PMID:
4690912
4.

Tay-Sachs disease--the use of tears for the detection of heterozygotes.

Carmody PJ, Rattazzi MC, Davidson RG.

N Engl J Med. 1973 Nov 15;289(20):1072-4. No abstract available.

PMID:
4742222
5.

Tay-Sachs disease: abbreviated serum hexosaminidase A test from finger-tip samples.

Cotlier E.

Clin Chim Acta. 1972 Apr;38(1):233-4. No abstract available.

PMID:
5031784
6.

Detection of Tay-Sachs disease heterozygotes by assay of hexosaminidase A in serum and leukocytes.

Suzuki Y, Berman PH, Suzuki K.

J Pediatr. 1971 Apr;78(4):643-7. No abstract available.

PMID:
5547820
7.

Human hexosaminidase isozymes: chromatographic separation as an aid to heterozygote identification.

Nakagawa S, Kumin S, Nitowsky HM.

Clin Chim Acta. 1977 Mar 1;75(2):181-91.

PMID:
851488
8.

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 17;2(7838):116-9. No abstract available.

PMID:
4128049
9.

Diagnosis of Tay-Sachs disease by hexosaminidase activity in leukocytes and amniotic fluid cells.

Padeh B, Navon R.

Isr J Med Sci. 1971 Feb;7(2):259-63. No abstract available.

PMID:
5560980
10.

Kinetic determination of hexosaminidases for Tay-Sachs heterozygote screening.

Zinterhofer L, Schuttringer G.

Clin Chem. 1976 Oct;22(10):1631-4.

PMID:
975509
11.
12.

Artificial substrates in the assay of acid glycosidases.

Hultbery B, Ockerman PA.

Clin Chim Acta. 1972 Jun;39(1):49-58. No abstract available.

PMID:
4624983
13.

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.

PMID:
6859103
14.

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. No abstract available.

PMID:
4433658
15.

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 16;77(1):43-52. No abstract available.

PMID:
872421
16.

Isoenzymes of serum N-acetyl-beta-D-glucosaminidase in the I cell disease heterozygote.

Van Elsen AF, Leroy JG, VanneuvilleFJ, Vercruyssen AL.

Hum Genet. 1976 Jan 28;31(1):75-81.

PMID:
174996
17.

Tay-Sachs carrier detection by mechanized serum hexosaminidase assay.

Rosenberg D, Cutler R.

Clin Chim Acta. 1974 Jun 19;53(2):247-53. No abstract available.

PMID:
4841990
19.

Marked variation in blood beta-hexosaminidase in Gaucher disease.

Natowicz MR, Prence EM, Cajolet A.

Clin Chim Acta. 1991 Nov 9;203(1):17-22.

PMID:
1837502

Supplemental Content

Support Center