[Diagnostic and therapeutic management of inherited metabolic diseases in emergency and intensive care unit]

Arch Pediatr. 2010 Jun;17(6):947-8. doi: 10.1016/S0929-693X(10)70192-5.
[Article in French]
No abstract available

MeSH terms

  • Adenosine Triphosphate / deficiency
  • Amino Acid Metabolism, Inborn Errors / diagnosis
  • Amino Acid Metabolism, Inborn Errors / therapy
  • Amino Acids / blood
  • Brain Diseases, Metabolic / diagnosis*
  • Brain Diseases, Metabolic / therapy
  • Carbohydrate Metabolism, Inborn Errors / diagnosis
  • Carbohydrate Metabolism, Inborn Errors / therapy
  • Coma / etiology
  • Coma / therapy
  • Critical Care*
  • Diagnosis, Differential
  • Emergency Service, Hospital*
  • France
  • Glycogen Storage Disease / diagnosis
  • Glycogen Storage Disease / therapy
  • Humans
  • Hypoglycemia / diagnosis
  • Hypoglycemia / etiology
  • Hypoglycemia / therapy
  • Infant, Newborn
  • Metabolism, Inborn Errors / diagnosis*
  • Metabolism, Inborn Errors / therapy*
  • Mitochondrial Diseases / diagnosis
  • Mitochondrial Diseases / therapy
  • Seizures / etiology
  • Seizures / therapy

Substances

  • Amino Acids
  • Adenosine Triphosphate