Urea Cycle Disorders: Diagnosis, Pathophysiology, and Therapy

Adv Pediatr. 1996;43:127-70.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Adolescent
  • Algorithms
  • Alkalosis, Respiratory / etiology*
  • Amino Acid Metabolism, Inborn Errors / diagnosis*
  • Amino Acid Metabolism, Inborn Errors / epidemiology
  • Amino Acid Metabolism, Inborn Errors / etiology
  • Amino Acid Metabolism, Inborn Errors / therapy*
  • Ammonia / blood*
  • Child
  • Female
  • Hepatic Encephalopathy / etiology*
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Ornithine Carbamoyltransferase Deficiency Disease
  • Pedigree
  • Treatment Outcome
  • Urea / metabolism*

Substances

  • Ammonia
  • Urea