Clinical biochemistry of peroxisomal disorders
- 31 March 1988
- journal article
- review article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 173 (1) , 57-80
- https://doi.org/10.1016/0009-8981(88)90357-9
Abstract
No abstract availableKeywords
This publication has 87 references indexed in Scilit:
- Conjugation of cholic acid with taurine and glycine by rat liver peroxisomesBiochemical and Biophysical Research Communications, 1986
- Pseudo-Zellweger syndrome: Deficiencies in several peroxisomal oxidative activitiesThe Journal of Pediatrics, 1986
- Peroxisomal dysfunction in a boy with neurologic symptoms and amaurosis (Leber disease): Clinical and biochemical findings similar to those observed in Zellweger syndromeThe Journal of Pediatrics, 1986
- Peroxisomal β-oxidation enzyme proteins in the Zellweger syndromeBiochemical and Biophysical Research Communications, 1985
- Deficiency of Enzymes Catalyzing the Biosynthesis of Glycerol-Ether Lipids in Zellweger SyndromeNew England Journal of Medicine, 1984
- The Cerebrohepatorenal (Zellweger) SyndromeNew England Journal of Medicine, 1984
- The cerebrohepatorenal syndrome of Zellweger, morphologic and metabolic aspectsAmerican Journal of Medical Genetics, 1983
- Hyperpipecolic acidemia: Clinical and biochemical observations in two male siblingsThe Journal of Pediatrics, 1981
- High concentration of hexacosanoate in cultured skin fibroblast lipids from adrenoleukodystrophy patientsBiochemical and Biophysical Research Communications, 1978
- Cerebro-hepato-renal syndrome of Zellweger: A report of eight cases with comments upon the incidence, the liver lesion, and a fault in pipecolic acid metabolismThe Journal of Pediatrics, 1975