Krabbe's Globoid Cell Leukodystrophy: Deficiency of Galactocerebrosidase in Serum, Leukocytes, and Fibroblasts

PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT

1951 • 319,299 citations

Globoid Cell Leucodystrophy (Krabbe's Disease): Deficiency of Galactocerebroside β-Galactosidase

1970 • 447 citations

Hurler's syndrome: biosynthesis of acid mucopolysaccharides in tissue culture.

1966 • 173 citations

Acid hydrolases in skin and plasma in gargoylism. Deficiency of β-galactosidase in skin

1968 • 111 citations

The use of white cells as a source of diagnostic material for lipid storage diseases

1969 • 88 citations

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

1971 • 51 citations

Galactosylgalactosylglucosylceramide: Galactosyl hydrolase in normal human plasma and its absence in patients with fabry's disease

1970 • 42 citations