Hyperdibasicaminoaciduria, hyperammonemia, and growth retardation: Treatment with arginine, lysine, and citrulline
- 30 November 1975
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 87 (5) , 731-738
- https://doi.org/10.1016/s0022-3476(75)80296-4
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
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- Hyperlysinuria With HyperammonemiaAmerican Journal of Diseases of Children, 1972
- Congenital lysinuria: A new inherited transport disorder of dibasic amino acidsThe Journal of Pediatrics, 1970
- Sequential Arginine and Insulin Tolerance Tests on the Same DayJournal of Clinical Endocrinology & Metabolism, 1969
- Hyperdibasicaminoaciduria: An Inherited Disorder of Amino Acid Transport[34]Pediatric Research, 1968
- FAMILIAL PROTEIN INTOLERANCE WITH DEFICIENT TRANSPORT OF BASIC AMINO ACIDSActa Medica Scandinavica, 1968
- Enzymes of Urea Synthesis in Familial Protein Intolerance with Deficient Transport of Basic Amino AcidsActa Paediatrica, 1967
- 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
- Rapid Wet Combustion Method for Carbon DeterminationAnalytical Chemistry, 1948