Ultrastructure and immunocytochemistry of hepatic peroxisomes in rhizomelic chondrodysplasia punctata
- 1 November 1992
- journal article
- case report
- Published by Springer Nature in European Journal of Pediatrics
- Vol. 151 (11) , 829-836
- https://doi.org/10.1007/bf01957935
Abstract
No abstract availableKeywords
This publication has 65 references indexed in Scilit:
- The inborn errors of peroxisomal β‐oxidation: A reviewJournal of Inherited Metabolic Disease, 1989
- Prenatal and perinatal diagnosis of peroxisomal disordersJournal of Inherited Metabolic Disease, 1989
- Rhizomelic chondrodysplasia punctata: Clinical, pathologic, and biochemical findings in two patientsThe Journal of Pediatrics, 1988
- Biochemical abnormalities in rhizomelic chondrodysplasia punctataThe Journal of Pediatrics, 1988
- 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
- Pseudo-Zellweger syndrome: Deficiencies in several peroxisomal oxidative activitiesThe Journal of Pediatrics, 1986
- Peroxisomal β-oxidation enzyme proteins in the Zellweger syndromeBiochemical and Biophysical Research Communications, 1985
- A simple post-embedding system for the rapid demonstration of tissue antigens under the electron microscopeJournal of Molecular Histology, 1983
- Cytochemistry of human catalase. The demonstration of hepatic and renal peroxisomes by a high temperature procedure.Journal of Histochemistry & Cytochemistry, 1979