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Phytanic acid
Ataxia with Loss of Purkinje Cells in a Mouse Model for Refsum Disease
LIPID METABOLISM-3 Regulation of Fatty Acid Oxidation
PHYH Gene Phytanoyl-Coa 2-Hydroxylase
Oxidation of Pristanic Acid in Fibroblasts and Its Application to the Diagnosis of Peroxisomal Beta-Oxidation Defects
Determining the Reference Intervals of Long-Chain Fatty Acids, Phytanic Acid and Pristanic Acid for Diagnostics of Peroxisome Disorders in Children
A Review of Odd-Chain Fatty Acid Metabolism and the Role of Pentadecanoic Acid (C15:0) and Heptadecanoic Acid (C17:0) in Health and Disease
Details About Three Fatty Acid Oxidation Pathways Occurring in Man
Phytol and Peroxisome Proliferation
Phytanic Acid Attenuates Insulin-Like Growth Factor-1 Activity Via Nitric
Phytanic Acid, a Daily Consumed Chlorophyll-Yielded Phytol Bio-Metabolite: a Comprehensive Review
A New Defect of Peroxisomal Function Involving Pristanic Acid: a Case Report B N Mclean, J Allen, S Ferdinandusse,Rjawanders
Oxidation of Fatty Acids
Peroxisomal Acyl-Coa Synthetases☆
Peroxisome Biogenesis Disorders in the Zellweger Spectrum: an Overview of Current Diagnosis, Clinical Manifestations, and Treatment Guidelines
Refsum Disease: the Presentation and Ophthalmic Aspects of Refsum Disease in a Series of 23 Patients
Fibroblast-Specific Genome-Scale Modelling Predicts an Imbalance in Amino Acid Metabolism in Refsum Disease
Chapter 20 Synthesis and Degradation of Lipids Chapter 20 Synthesis and Degradation of Lipids
Inherited Metabolic Disorders Presenting with Ataxia
Top View
Localization of the Oxidative Defect in Phytanic Acid Degradation in Patients with Refsum's Disease
Alpha-Oxidation ⁎ Gerbert A
Peroxisome Metabolism in Cancer
Utilization of Sterol Carrier Protein-2 by Phytanoyl-Coa 2-Hydroxylase in the Peroxisomal Oxidation of Phytanic Acid
Decompensation of Refsum Disease Caused by Ibuprofen Intake Natacha Esber, M.D
Infantile Refsum Disease Commentary
Studies on the Metabolic Error in Refsum's Disease