Turnover of beta-galactosidase in fibroblasts from patients with genetically different types of beta-galactosidase deficiency.

Por Van Diggelen, O P, Schram, A W, Sinnott, M L, Smith, P J, Robinson, D, Galjaard, H
Publicado em 1981

Biosynthesis and maturation of peroxisomal beta-oxidation enzymes in fibroblasts in relation to the Zellweger syndrome and infantile Refsum disease.

Por Schram, A W, Strijland, A, Hashimoto, T, Wanders, R J, Schutgens, R B, van den Bosch, H, Tager, J M
Publicado em 1986

Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementa...

Por Brul, S, Westerveld, A, Strijland, A, Wanders, R J, Schram, A W, Heymans, H S, Schutgens, R B, van den Bosch, H, Tager, J M
Publicado em 1988

Comparative study on glucocerebrosidase in spleens from patients with Gaucher disease.

Por Aerts, J M, Donker-Koopman, W E, Brul, S, Van Weely, S, Sa Miranda, M C, Barranger, J A, Tager, J M, Schram, A W
Publicado em 1990

Peroxisomal fatty acid beta-oxidation in relation to the accumulation of very long chain fatty acids in cultured skin fibroblasts from patients with Zellweger syndrome and other pe...

Por Wanders, R J, van Roermund, C W, van Wijland, M J, Schutgens, R B, Heikoop, J, van den Bosch, H, Schram, A W, Tager, J M
Publicado em 1987

Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency.

Por Schram, A W, Goldfischer, S, van Roermund, C W, Brouwer-Kelder, E M, Collins, J, Hashimoto, T, Heymans, H S, van den Bosch, H, Schutgens, R B, Tager, J M
Publicado em 1987