Biochemical Analysis in Peroxisomal Disorders

This publication has 15 references indexed in Scilit:

• Lignoceroyl‐CoASH ligase: enzyme defect in fatty acid β‐oxidation system in X‐linked childhood adrenoleukodystrophy
  FEBS Letters, 1986
• Dysmorphic syndrome with phytanic acid oxidase deficiency, abnormal very long chain fatty acids, and pipecolic acidemia: Studies in four children
  The Journal of Pediatrics, 1986
• Pseudo-Zellweger syndrome: Deficiencies in several peroxisomal oxidative activities
  The 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 syndrome
  The Journal of Pediatrics, 1986
• Peroxisomal matrix enzymes in zellweger syndrome: Activity and subcellular localization in liver
  Journal of Inherited Metabolic Disease, 1985
• Peroxisomal β-oxidation enzyme proteins in the Zellweger syndrome
  Biochemical and Biophysical Research Communications, 1985
• The cerebro-hepato-renal (Zellweger) syndrome. Impaired de novo biosynthesis of plasmalogens in cultured skin fibroblasts
  Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1985
• Adrenoleukodystrophy: Survey of 303 cases: Biochemistry, diagnosis, and therapy
  Annals of Neurology, 1984
• Activity of peroxisomal enzymes and intracellular distribution of catalase in Zellweger syndrome
  Biochemical and Biophysical Research Communications, 1984
• The Cerebrohepatorenal (Zellweger) Syndrome
  New England Journal of Medicine, 1984