Treatment of hyperammonemic coma caused by inborn errors of urea synthesis
- 1 December 1980
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 97 (6), 893-900
- https://doi.org/10.1016/s0022-3476(80)80416-1
Abstract
No abstract availableThis publication has 38 references indexed in Scilit:
- The management of life-threatening hyperammonemia: A comparison of several therapeutic modalitiesThe Journal of Pediatrics, 1980
- Comparison of exchange transfusion, peritoneal dialysis, and hemodialysis for the treatment of hyperammonemia in an anuric newborn infantThe Journal of Pediatrics, 1979
- Transient Hyperammonemia of the Preterm InfantNew England Journal of Medicine, 1978
- Treatment of complete ornithine transcarbamylase deficiency with nitrogen-free analogues of essential amino acidsThe Journal of Pediatrics, 1978
- Neonatal citrullinemia: Treatment with keto-analogues of essential amino acidsThe Journal of Pediatrics, 1977
- Peritoneal dialysis and exchange transfusion in a neonate with argininosuccinic aciduria.Archives of Disease in Childhood, 1976
- HEREDITARY ORNITHINE TRANSCARBAMYLASE DEFICIENCYActa Paediatrica, 1975
- Ornitbine transcarbamylase deficiency in the newborn infantThe Journal of Pediatrics, 1973
- Infusion of protein hydrolysates in the newborn infant: Plasma amino acid concentrationsThe Journal of Pediatrics, 1971
- Nonketotic hyperglycinemiaThe Journal of Pediatrics, 1969