Apparent deficiency of hexosaminidase A in healthy members of a family with Tay-Sachs disease.

Tay-Sachs Disease: Generalized Absence of a Beta-D- N -Acetylhexosaminidase Component

1969 • 707 citations

N-Acetyl-β-glucosaminidases in human spleen

1968 • 523 citations

[Tay-Sachs disease].

1973 • 390 citations

Tay-Sachs Disease: Prenatal Diagnosis

1971 • 177 citations

PRENATAL DIAGNOSIS OF TAY-SACHS DISEASE

1970 • 125 citations

Ganglioside GM2 storage diseases: hexosaminidase deficiencies in cultured fibroblasts.

1971 • 81 citations

The hydrolysis of Tay‐Sachs ganglioside (TSG) by human N‐acetyl‐β‐D‐hexosaminidase A

1970 • 65 citations

Juvenile GM2 gangliosidosis: Partial deficiency of bexosaminidase A

1970 • 64 citations

Identification of tay-sachs disease carriers by acrylamide gel electrophoresis

1970 • 54 citations

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

1971 • 51 citations

Prenatal Diagnosis of Tay-Sachs Genotypes

1971 • 37 citations

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

1971 • 30 citations

Urinary test for identification of Tay-Sachs genotypes

1972 • 26 citations