α-Oxidation as an alternative pathway for the degradation of branched-chain fatty acids in man, and its failure in patients with refsum's disease
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Biochemistry,Biophysics
Reference29 articles.
1. Über das Vorkommen der 3.7.11.15-Tetramethyl-hexadecansäure (Phytansäure) in den Cholesterinestern und anderen Lipoidfraktionen der Organe bei einem Krankheitsfall unbekannter Genese (Verdacht auf Heredopathia atactica polyneuritiformis [Refsum-Syndrom])
2. Refsum-Syndrom. ? Lipoidchemische Untersuchungen bei 9 F�llen
3. 3,7,11, 15-Tetramethylhexadecanoic acid: ITs occurrence in the tissues of humans afflicted with refsum's syndrome
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1. Adult Refsum Disease in Puerto Rico: A Case Report;Cureus;2023-09-17
2. Heredopathia atactica polyneuritiformis: Refsum's disease;Acta Neurologica Scandinavica;2009-01-29
3. Further studies on the substrate spectrum of phytanoyl-CoA hydroxylase;Journal of Lipid Research;2003-12
4. Phytanic acid alpha-oxidation, new insights into an old problem: a review;Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids;2003-03
5. Phytanic acid storage disease (Refsum's disease): Clinical characteristics, pathophysiology and the role of therapeutic apheresis in its management;Journal of Clinical Apheresis;1999
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