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Neonatal hemodialysis: effective therapy for the encephalopathy of inborn errors of metabolism.

AuthorsS L Rutledge, P L Havens, M W Haymond, R H McLean, J S Kan, S W Brusilow
JournalThe Journal of pediatrics (J Pediatr) Vol. 116 Issue 1 Pg. 125-8 (Jan 1990) ISSN: 0022-3476 [Print] United States
PMID2295952 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Amino Acids, Branched-Chain
  • Keto Acids
  • Glutamine
  • Ammonia
  • Ligases
  • Argininosuccinate Synthase
Topics
  • Amino Acid Metabolism, Inborn Errors (complications)
  • Amino Acids, Branched-Chain (metabolism)
  • Ammonia (metabolism)
  • Argininosuccinate Synthase (deficiency)
  • Brain Diseases, Metabolic (etiology, therapy)
  • Female
  • Glutamine (metabolism)
  • Humans
  • Infant, Newborn
  • Keto Acids (metabolism)
  • Ligases (deficiency)
  • Male
  • Maple Syrup Urine Disease (complications)
  • Renal Dialysis

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