Elisabeth M. Brouwer-Kelder

Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency.

A. W. Schram, Sidney Goldfischer, C W van Roermund et al. · Proceedings of the National Academy of Sciences · 1987 · 203 citations · Full text

Life Sciences, Biochemistry, Cellular Metabolism +16

Presence of peroxisomal membrane proteins in liver and fibroblasts from patients with the Zellweger syndrome and related disorders: evidence for the existence of peroxisomal ghosts.

Erik A.C. Wiemer, Stanley Brul, Just Ww et al. · PubMed · 1989 · 81 citations

Medicine, Biochemistry, Pathology +13

X-Linked adrenoleukodystrophy: Defective peroxisomal oxidation of very long chain fatty acids but not of very long chain fatty acyl-CoA esters

R. J. A. Wanders, C. W. T. van Roermund, M.J.A. van Wijland et al. · Clinica Chimica Acta · 1987 · 57 citations

Life Sciences, Biochemistry, Endocrinology +16

Isolation and characterization of a precursor form of lysosomal α‐glucosidase from human urine

Ronald P.J. Oude Elferink, Elisabeth M. Brouwer-Kelder, Inge SURYA et al. · European Journal of Biochemistry · 1984 · 56 citations

Life Sciences, Biochemistry, Molecular Biology +7

Clinical phenotype of Gaucher disease in relation to properties of mutant glucocerebrosidase in cultured fibroblasts

Sonja van Weely, M.B. van Leeuwen, Ineke D.C. Jansen et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 1991 · 52 citations

Life Sciences, Biochemistry, Genetics +13