Hereditary Hyperammonaemic Syndromes — A Six Year Experience
- 1 September 1979
- journal article
- case report
- Published by Wiley in Journal of Paediatrics and Child Health
- Vol. 15 (3) , 142-146
- https://doi.org/10.1111/j.1440-1754.1979.tb01212.x
Abstract
No abstract availableThis publication has 20 references indexed in Scilit:
- 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
- Carrier detection in ornithine transcarbamylase deficiencyThe Journal of Pediatrics, 1978
- Severe hyperammonemia in a newborn infant with methylmalonyl-CoA mutase deficiencyThe Journal of Pediatrics, 1978
- Abnormal metabolites of isoleucine in a patient with propionyl-CoA carboxylase deficiencyJournal of Mass Spectrometry, 1978
- Propionic acidemia with severe hyperammonemia and defective glycine metabolismThe Journal of Pediatrics, 1978
- Neonatal citrullinemia: Treatment with keto-analogues of essential amino acidsThe Journal of Pediatrics, 1977
- Severe neonatal citrullinaemia.Archives of Disease in Childhood, 1974
- Familial Protein Intolerance with Deficient Transport of Basic Amino Acids: An Analysis of 10 PatientsActa Paediatrica, 1967
- Congenital lysine intolerance with periodic ammonia intoxication: A defect in L-lysine degradationMetabolism, 1967