A. W. Schram

A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy).

Bwee Tien Poll‐The, Frank Roels, H. Ogier et al. · PubMed · 1988 · 262 citations

Life Sciences, Biochemistry, Endocrinology +17

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

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

Stanley Brul, A. Westerveld, Anneke Strijland et al. · Journal of Clinical Investigation · 1988 · 164 citations · Full text

Life Sciences, Biochemistry, Genetics +16

Direct demonstration that the deficient oxidation of very long chain fatty acids in X-linked adrenoleukodystrophy is due to an impaired ability of peroxisomes to activate very long chain fatty acids

R. J. A. Wanders, Carlo W.T. van Roermund, M.J.A. van Wijland et al. · Biochemical and Biophysical Research Communications · 1988 · 159 citations

Life Sciences, Biochemistry, Molecular Genetics +17

Infantile Refsum disease: an inherited peroxisomal disorder

Bwee Tien Poll‐The, J. M. Saudubray, H. Ogier et al. · European Journal of Pediatrics · 1987 · 132 citations

Life Sciences, Genetics, Pediatrics +9