Peroxisomal dysfunction in a boy with neurologic symptoms and amaurosis (Leber disease): Clinical and biochemical findings similar to those observed in Zellweger syndrome
- 1 January 1986
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 108 (1), 19-24
- https://doi.org/10.1016/s0022-3476(86)80763-6
Abstract
No abstract availableThis publication has 30 references indexed in Scilit:
- Adrenoleukodystrophy: Survey of 303 cases: Biochemistry, diagnosis, and therapyAnnals of Neurology, 1984
- Disturbed adrenocortical function in cerebro-hepato-renal syndrome of ZellwegerEuropean Journal of Pediatrics, 1984
- POSSIBILITY OF PRENATAL DIAGNOSIS OF ZELLWEGER SYNDROMEThe Lancet, 1984
- The Cerebrohepatorenal (Zellweger) SyndromeNew England Journal of Medicine, 1984
- Hepatic Uptake of Bile Acids in ManJournal of Clinical Investigation, 1982
- Conversion of 3α,7α,12α‐trihydroxy‐5β‐cholestanoic acid into cholic acid by rat liver peroxisomesFEBS Letters, 1980
- C27 Bile Acids in Infants with Coprostanic Acidemia and Occurrence of a 3alpha,7alpha,12alpha-Trihydroxy-5beta-C29 Dicarboxylic Bile Acid as a Major Component in Their SerumEuropean Journal of Biochemistry, 1979
- Defects of Bile Acid Synthesis in Zellweger's SyndromeScience, 1979
- Studies on microperoxisomes. VII. Pigment epithelial cells and other cell types in the retina of rodents.The Journal of cell biology, 1975
- Trihydroxycoprostanic acid in the duodenal fluid of two children with intrahepatic bile duct anomaliesBiochimica et Biophysica Acta (BBA) - General Subjects, 1972