[Metabolic myopathies--part I: disorders of the carbohydrate metabolism]

MeSH terms

• Carbohydrate Metabolism / physiology
• Carbohydrate Metabolism, Inborn Errors / classification
• Carbohydrate Metabolism, Inborn Errors / genetics
• Carbohydrate Metabolism, Inborn Errors / pathology*
• Fructose-Bisphosphate Aldolase / deficiency
• Fructose-Bisphosphate Aldolase / genetics
• Glycogen / deficiency
• Glycogen / metabolism
• Glycogen Storage Disease Type II / genetics
• Glycogen Storage Disease Type II / metabolism
• Glycogen Storage Disease Type III / genetics
• Glycogen Storage Disease Type III / metabolism
• Glycogen Storage Disease Type IV / genetics
• Glycogen Storage Disease Type IV / metabolism
• Glycogen Storage Disease Type V / genetics
• Glycogen Storage Disease Type V / metabolism
• Glycogen Storage Disease Type VII / genetics
• Glycogen Storage Disease Type VII / metabolism
• Glycogen Storage Disease Type VIII / genetics
• Glycogen Storage Disease Type VIII / metabolism
• Humans
• L-Lactate Dehydrogenase / deficiency
• Mitochondrial Myopathies / classification
• Mitochondrial Myopathies / genetics
• Mitochondrial Myopathies / pathology*
• Phosphoglycerate Kinase / deficiency
• Phosphoglycerate Mutase / deficiency
• Phosphoglycerate Mutase / genetics
• Phosphorylase b / deficiency