Hyperammonaemia. A variant type of deficiency of liver ornithine transcarbamylase.
Open Access
- 1 April 1969
- journal article
- research article
- Published by BMJ in Archives of Disease in Childhood
- Vol. 44 (234) , 162-169
- https://doi.org/10.1136/adc.44.234.162
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Hyperammonaemia: a deficiency of liver ornithine transcarbamylase. Occurrence in mother and child.Archives of Disease in Childhood, 1969
- Fructosaemia: Observations on seven casesThe American Journal of Medicine, 1968
- Familial Protein Intolerance with Deficient Transport of Basic Amino Acids: An Analysis of 10 PatientsActa Paediatrica, 1967
- Arginosuccine aciduria.1967
- Treatment of HyperammonemiaArchives of Pediatrics & Adolescent Medicine, 1967
- PROTEIN INTOLERANCE WITH DEFICIENT TRANSPORT OF BASIC AMINOACIDSThe Lancet, 1965
- On the determination of ornithine-carbamyl-transferase activityClinica Chimica Acta; International Journal of Clinical Chemistry, 1964
- HYPERAMMONÆMIAThe Lancet, 1962
- Pathogenesis and management of hepatic comaThe American Journal of Medicine, 1958
- Episodic Stupor Associated with an Eck Fistula in the Human with Particular Reference to the Metabolism of Ammoniaxs12Journal of Clinical Investigation, 1954