Periodic attacks of lethargy in a baby with ammonia intoxication due to a congenital defect in ureogenesis.
Open Access
- 1 December 1969
- journal article
- research article
- Published by BMJ in Archives of Disease in Childhood
- Vol. 44 (238) , 681-687
- https://doi.org/10.1136/adc.44.238.681
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
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- Hyperammonaemia Due to Ornithine Transcarbamylase DeficiencyArchives of Disease in Childhood, 1969
- Hereditary orotic aciduria. II. A urinary screening test.1968
- Congenital lysine intolerance with periodic ammonia intoxication: A defect in L-lysine degradationMetabolism, 1967
- [Periodic stupor and ammonia intoxication in a child with anicteric subacute hepatitis].1967
- ARGININOSUCCINATE SYNTHETASE ACTIVITY AND CITRULLINE METABOLISM IN CELLS CULTURED FROM A CITRULLINEMIC SUBJECTProceedings of the National Academy of Sciences, 1967
- Ammonia intoxication due to acongenital defect in urea synthesisThe Journal of Pediatrics, 1964
- Mikromethode zur Bestimmung der Ornithin-Carbamoyl-Transferase (OCT) in Serum und LiquorKlinische Wochenschrift, 1963
- HYPERAMMONÆMIAThe Lancet, 1962