Inherent lipid metabolic dysfunction in glycogen storage disease IIIa

Medicine & Life Sciences

• Glycogen Storage Disease 100%
• 4 alpha-glucanotransferase 88%
• Lipids 45%
• Fatty Acids 44%
• Medium chain acyl CoA dehydrogenase deficiency 29%
• Glucosidases 26%
• Peroxisome Proliferator-Activated Receptors 21%
• Genes 21%
• Gene Expression 20%
• Hepatomegaly 20%
• Intra-Abdominal Fat 19%
• Mutation 19%
• Heterozygote 18%
• Muscle Weakness 18%
• Nonesterified Fatty Acids 18%
• Gene Expression Profiling 18%
• Liver 18%
• Hyperlipidemias 17%
• Human Herpesvirus 4 17%
• Hypoglycemia 16%
• Inborn Genetic Diseases 16%
• Metabolic Syndrome 16%
• Hepatocytes 14%
• B-Lymphocytes 13%
• Parents 13%
• Phenotype 10%
• Proteins 6%

Chemical Compounds

• Glycogen 83%
• Metabolic 56%
• Fatty Acid 56%
• Lipid 48%
• Mutation 39%
• Acyl-CoA 30%
• Fat 23%
• Disorder 19%
• Biosynthesis 19%
• Oxidation Reaction 10%
• Protein 9%