Zellweger-like syndrome with detectable hepatic peroxisomes: A variant form of peroxisomal disorder
- 1 November 1988
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 113 (5) , 841-845
- https://doi.org/10.1016/s0022-3476(88)80011-8
Abstract
No abstract availableFunding Information
- Ministry of Health, Labour and Welfare (62-6)
- National Center of Neurology and Psychiatry
- Ministry of Education, Culture, Sports, Science and Technology
This publication has 11 references indexed in Scilit:
- Molecular analysis of peroxisomal β-oxidation enzymes in infants with Zellweger syndrome and Zellweger-like syndrome: Further heterogeneity of the peroxisomal disorderClinica Chimica Acta; International Journal of Clinical Chemistry, 1988
- Age-related accumulation of phytanic acid in plasma from patients with the cerebro-hepato-renal (Zellweger) syndromeClinica Chimica Acta; International Journal of Clinical Chemistry, 1987
- Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency.Proceedings of the National Academy of Sciences, 1987
- Peroxisomal disorders: A newly recognised group of genetic diseasesEuropean Journal of Pediatrics, 1986
- Pseudo-Zellweger syndrome: Deficiencies in several peroxisomal oxidative activitiesThe Journal of Pediatrics, 1986
- Infantile Refsum's disease (phytanic acid storage disease): a variant of Zellweger's syndrome?Clinical Genetics, 1984
- Deficiency of acyl-CoA: Dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndromeBiochemical and Biophysical Research Communications, 1984
- Light microscopic immunocytochemical demonstration of peroxisomal enzymes in epon sectionsHistochemistry and Cell Biology, 1984
- Abnormality of Long‐Chain Fatty Acids in Erythrocyte Membrane Sphingomyelin from Patients with AdrenoleukodystrophyJournal of Neurochemistry, 1981
- Peroxisomal and Mitochondrial Defects in the Cerebro-Hepato-Renal SyndromeScience, 1973