Zellweger‐like phenotype in two siblings: A defect in peroxisomal β‐oxidation with elevated very long‐chain fatty acids but normal bile acids

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

Peroxisomal bifunctional enzyme deficiency.

Paul A. Watkins, W W Chen, Civonnia Harris et al. · Journal of Clinical Investigation · 1989 · 210 citations · Full text

Life Sciences, Biochemistry, Cellular Biochemistry +16

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

Separate peroxisomal oxidases for fatty acyl-CoAs and trihydroxycoprostanoyl-CoA in human liver

Minne Casteels, L Schepers, PP Van Veldhoven et al. · Journal of Lipid Research · 1990 · 59 citations · Full text

Life Sciences, Biochemistry, Cellular Metabolism +12

Neonatal seizures and retardation in a girl with biochemical features of X‐linked adrenoleukodystrophy

S. Naidu, Gerald Höefler, Paul A. Watkins et al. · Neurology · 1988 · 50 citations

Medicine, Endocrinology, Pediatrics +17