The mechanism of hyperammonemia in congenital lysinuria
- 28 February 1979
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 94 (2) , 255-257
- https://doi.org/10.1016/s0022-3476(79)80838-0
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Hyperdibasicaminoaciduria, hyperammonemia, and growth retardation: Treatment with arginine, lysine, and citrullineThe Journal of Pediatrics, 1975
- Diamino Acid Transport into Granulocytes and Liver Slices of Patients with Lysinuric Protein IntolerancePediatric Research, 1975
- Defective metabolic clearance of plasma arginine and ornithine in lysinuric protein intoleranceMetabolism, 1974
- Hyperlysinuria With HyperammonemiaAmerican Journal of Diseases of Children, 1972
- Congenital lysinuria: A new inherited transport disorder of dibasic amino acidsThe Journal of Pediatrics, 1970
- Methionine and Glycine Levels in the Liver of Riboflavin Deficient RatsThe Tohoku Journal of Experimental Medicine, 1968
- Familial Protein Intolerance with Deficient Transport of Basic Amino Acids: An Analysis of 10 PatientsActa Paediatrica, 1967
- PROTEIN INTOLERANCE WITH DEFICIENT TRANSPORT OF BASIC AMINOACIDSThe Lancet, 1965