Human liver pathology in peroxisomal diseases: A review including novel data
- 24 January 1993
- Vol. 75 (3-4) , 281-292
- https://doi.org/10.1016/0300-9084(93)90088-a
Abstract
No abstract availableKeywords
This publication has 79 references indexed in Scilit:
- Acyl‐CoA oxidase, peroxisomal thiolase and dihydroxyacetone phosphate acyltransferase: Aberrant subcellular localization in Zellweger syndromeJournal of Inherited Metabolic Disease, 1990
- Pathology of hepatic peroxisomes and mitochondria in patients with peroxisomal disordersVirchows Archiv, 1990
- Immunocytochemical detection of peroxisomal β-oxidation enzymes in cryostat and paraffin sections of human post mortem liverJournal of Molecular Histology, 1990
- Altered acyl-CoA metabolism in riboflavin deficiencyBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1989
- Significance of catalase in peroxisomal fatty acyl-CoA β-oxidationBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1987
- Biosynthesis of peroxisomal β-oxidation enzymes in infants with zellweger syndromeJournal of Inherited Metabolic Disease, 1986
- Peroxisomal abnormalities in rhizomelic chondrodysplasia punctataJournal of Inherited Metabolic Disease, 1986
- Peroxisomes in infantile phytanic acid storage disease: a cytochemical study of skin fibroblastsJournal of Inherited Metabolic Disease, 1986
- Infantile phytanic acid storage disease, a possible variant of Refsum's disease: Three cases, including ultrastructural studies of the liverJournal of Inherited Metabolic Disease, 1982
- Cytochemistry of human catalase. The demonstration of hepatic and renal peroxisomes by a high temperature procedure.Journal of Histochemistry & Cytochemistry, 1979