Hyperammonaemia in 20 families. Biochemical and genetical survey, including investigations in 3 new families.
Open Access
- 1 June 1974
- journal article
- research article
- Published by BMJ in Archives of Disease in Childhood
- Vol. 49 (6) , 443-449
- https://doi.org/10.1136/adc.49.6.443
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
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- Ornithine Transcarbamylase DeficiencyNew England Journal of Medicine, 1973
- LETHAL NEONATAL HYPERAMMONÆMIA DUE TO COMPLETE ORNITHINE-TRANSCARBAMYLASE DEFICIENCYThe Lancet, 1971
- Hereditary Metabolic Disorders of the Urea CyclePublished by Elsevier ,1971
- Periodic attacks of lethargy in a baby with ammonia intoxication due to a congenital defect in ureogenesis.Archives of Disease in Childhood, 1969
- BIOCHEMICAL INVESTIGATIONS OF HYPERAMMONÆMIAThe Lancet, 1969
- Hyperammonaemia. A variant type of deficiency of liver ornithine transcarbamylase.Archives of Disease in Childhood, 1969
- Hyperammonaemia: a deficiency of liver ornithine transcarbamylase. Occurrence in mother and child.Archives of Disease in Childhood, 1969
- Hyperammonaemia Due to Ornithine Transcarbamylase DeficiencyArchives of Disease in Childhood, 1969
- HYPERAMMONÆMIAThe Lancet, 1962