Very large peroxisomes in distinct peroxisomal disorders (rhizomelic chondrodysplasia punctata and acyl-CoA oxidase deficiency): novel data
- 1 November 1991
- journal article
- case report
- Published by Springer Nature in Virchows Archiv
- Vol. 419 (6) , 523-525
- https://doi.org/10.1007/bf01650683
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Hepatocellular peroxisomes in human alcoholic and drug-induced hepatitis: A quantitative studyHepatology, 1991
- Clinical variation in X-linked adrenoleukodystrophy: Fatty acid and lipid metabolism in cultured fibroblastsBiochemical Medicine and Metabolic Biology, 1991
- Central Nervous System Malformations and White Matter Changes in Pseudo-Neonatal Adrenoleukodystrophy*Neuropediatrics, 1990
- Pathology of hepatic peroxisomes and mitochondria in patients with peroxisomal disordersVirchows Archiv, 1990
- Heterogeneity of catalase staining in human hepatocellular peroxisomes.Journal of Histochemistry & Cytochemistry, 1989
- Automated image analysis of rat liver peroxisomes after treatment with thyroid hormones: Changes in number, size and catalase reactionMicron and Microscopica Acta, 1989
- Rhizomelic chondrodysplasia punctata: Clinical, pathologic, and biochemical findings in two patientsThe Journal of Pediatrics, 1988
- Neonatal seizures and retardation in a girl with biochemical features of X‐linked adrenoleukodystrophyNeurology, 1988
- Light microscopic visualization of peroxisomes and plasmalogens in first trimester chorionic villiPrenatal Diagnosis, 1987
- Peroxisomal abnormalities in rhizomelic chondrodysplasia punctataJournal of Inherited Metabolic Disease, 1986