• Inborn errors of metabolism: Classification
  View in Chinese
  • Fatty acid oxidation disorders
  • Summary
  • Disorders of fatty acid oxidation (Tables)
  • Laboratory findings inborn errors of metabolism (Tables)
• Approach to hypoglycemia in infants and children
  • Interpretation of results
  • Summary and recommendations
• Metabolic myopathies caused by disorders of lipid and purine metabolism
  View in Chinese
  • Summary
• Inborn errors of metabolism: Metabolic emergencies
  View in Chinese
  • Hypoglycemia
  • SIDS or ALTE
  • Summary
• Inborn errors of metabolism: Epidemiology, pathogenesis, and clinical features
  • Cardiomyopathy
  • Abnormal tone
  • Summary
• Approach to the metabolic myopathies
  View in Chinese
  • Disorders of lipid metabolism
  • Summary and recommendations
• Inborn errors of metabolism: Identifying the specific disorder
  View in Chinese
  • Acylcarnitine profile
  • Cardiomyopathy
  • Summary and recommendations
• Causes of hypoglycemia in infants and children
  View in Chinese
  • Disorders of fatty acid metabolism
  • Ketotic hypoglycemia
  • Summary
• Sudden unexpected infant death including SIDS: Initial management
  • Metabolic disease
  • Summary and recommendations
• Acute liver failure in children: Etiology and evaluation
  View in Chinese
  • Summary and recommendations
• Approach to the infant with hypotonia and weakness
  View in Chinese
  • Physical examination
  • Summary and recommendations
• Myophosphorylase deficiency (glycogen storage disease V, McArdle disease)
  View in Chinese
  • Differential diagnosis
  • Summary and recommendations
• Urea cycle disorders: Clinical features and diagnosis
  View in Chinese
  • Summary
• Organic acidemias
  View in Chinese
  • Summary
• Evaluation of weight loss in infants six months of age and younger
  View in Chinese
  • Physical examination
  • Summary and recommendations
• Lysosomal acid alpha-glucosidase deficiency (Pompe disease, glycogen storage disease II, acid maltase deficiency)
  View in Chinese
  • Differential diagnosis
  • Summary
• Acute toxic-metabolic encephalopathy in children
  View in Chinese
  • Reye syndrome
  • Summary and recommendations
• Classification and causes of jaundice or asymptomatic hyperbilirubinemia
  View in Chinese
  • Summary and recommendations
• Approach to the ill-appearing infant (younger than 90 days of age)
  View in Chinese
  • Summary and recommendations
• Cyclic vomiting syndrome
  View in Chinese
  • Summary and recommendations
• Juvenile dermatomyositis and polymyositis: Diagnosis
  View in Chinese
  • Summary and recommendations
• Causes and clinical manifestations of primary adrenal insufficiency in children
  View in Chinese
  • Summary
• Dravet syndrome: Management and prognosis
  • Summary and recommendations
• Etiology of hypocalcemia in infants and children
  View in Chinese
  • Genetic mechanisms
  • Summary
• Overview of peripheral nerve and muscle disorders causing hypotonia in the newborn
  View in Chinese
  • Summary
• Causes of cholestasis in neonates and young infants
  • Summary
• Carnitine metabolism in renal disease and dialysis
  • Summary and recommendations

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