Medium-chain acyl-CoA dehydrogenase deficiency in children with non-ketotic hypoglycemia and low carnitine levels

Keyphrases

• Fatty Acid Oxidation 100%
• Medium-chain acyl-CoA Dehydrogenase 100%
• Medium-chain acyl-CoA Dehydrogenase Deficiency 100%
• Acyl-CoA Dehydrogenase 100%
• Illness 66%
• Electron Transfer Flavoprotein 66%
• L-carnitine 66%
• Carnitine Deficiency 66%
• Dehydrogenase Complex 33%
• Liver 33%
• Fatty Acids 33%
• Free Fatty Acids 33%
• Low Dose Rate 33%
• Coma 33%
• Early childhood 33%
• Dicarboxylic Acids 33%
• Cerebral Edema 33%
• Short-chain Fatty Acids 33%
• Ketones 33%
• Inherited Metabolic Diseases 33%
• Hypoglycemia 33%
• One-child 33%
• Normal Rate 33%
• Short Chain 33%
• Ketogenesis 33%
• Long-chain Fatty Acids 33%
• Medium-chain Fatty Acids 33%
• Acyl-CoA 33%
• Liver Tissue 33%
• Fatty Liver 33%
• Reye Syndrome 33%
• All Media 33%
• Normal Activity 33%
• Hyperammonemia 33%
• β-hydroxybutyrate 33%
• New Assay 33%
• Plasma beta 33%

Pharmacology, Toxicology and Pharmaceutical Science

• Hypoglycemia 100%
• Carnitine 100%
• Acyl Coenzyme A Dehydrogenase 100%
• Fatty Acid 75%
• Disease 25%
• Electron Transferring Flavoprotein 25%
• Carnitine Deficiency 25%
• Epileptic Absence 12%
• Clinical Study 12%
• Mole (Insectivora) 12%
• Ketoacidosis 12%
• Acyl-CoA 12%
• Long Chain Fatty Acid 12%
• Coma 12%
• Metabolic Disorder 12%
• Hyperammonemia 12%
• Long Chain Acyl Coenzyme A Dehydrogenase 12%
• Medium Chain Fatty Acid 12%
• Short Chain Fatty Acid 12%
• Fatty Liver 12%
• Dicarboxylic Acid 12%
• Octanoyl-CoA 12%
• Brain Edema 12%

Biochemistry, Genetics and Molecular Biology

• Medium-Chain Acyl-CoA Dehydrogenase 100%
• Acyl-CoA 100%
• Beta Oxidation 50%
• Electron Transport 20%
• Flavoprotein 20%
• Oxidoreductase 10%
• Dehydrogenase 10%
• Metabolic Disorder 10%
• Ketogenesis 10%
• Coma 10%
• Mole (Insectivora) 10%
• Clinical Study 10%
• Free Fatty Acids 10%
• Short-Chain Fatty Acid 10%