Urinary Dicarboxylic Acids in X-Linked Adrenoleukodystrophy
Author:
Publisher
Wiley
Subject
Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1442-200X.1990.tb00822.x/fullpdf
Reference10 articles.
1. Compartmentation of dicarboxylic acid β-oxidation in rat liver: importance of peroxisomes in the metabolism of dicarboxylic acids
2. Peroxisomal disorders: A newly recognised group of genetic diseases
3. Adrenoleukodystrophy and other peroxisomal disorders that affect the nervous system, including new observations on L-pipecolic acid oxidase in primates
4. Urinary excretion of dicarboxylic acids from patients with the zellweger syndrome Importance of peroxisomes in β-oxidation of dicarboxylic acids
5. Medium- and Long-Chain Dicarboxylic Aciduria in Patients with Zellweger Syndrome and Neonatal Adrenoleukodystrophy
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1. Hepatic dysfunction in peroxisomal disorders;Biochimica et Biophysica Acta (BBA) - Molecular Cell Research;2016-05
2. Single Peroxisomal Enzyme and Transporter Deficiencies in Human Diseases and Mouse Models;Molecular Machines Involved in Peroxisome Biogenesis and Maintenance;2014
3. Metabolic disposition and elimination studies of a radiolabelled biodegradable polymeric implant in the rat brain;Biomaterials;1994-01
4. Excretion of 3,6-epoxydicarboxylic acids in peroxisomal disorders;Clinica Chimica Acta;1993-12
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