Amino acid levels in patients with hyperammonaemia and argininosuccinic aciduria
- 17 May 1974
- journal article
- research article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 52 (3) , 335-341
- https://doi.org/10.1016/0009-8981(74)90119-3
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Hyperammonaemia in 20 families. Biochemical and genetical survey, including investigations in 3 new families.Archives of Disease in Childhood, 1974
- BIOCHEMICAL INVESTIGATIONS OF HYPERAMMONÆMIAThe Lancet, 1969
- Technical pitfalls leading to errors in the quantitation of plasma amino acidsClinica Chimica Acta; International Journal of Clinical Chemistry, 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
- Amino-acids on HandsNature, 1965
- HYPERAMMONÆMIAThe Lancet, 1962
- Argininosuccinic Aciduria: An Inborn Error of Amino Acid MetabolismArchives of Disease in Childhood, 1961
- Argininosuccinase Activity in Brain TissueNature, 1960
- A DISEASE, PROBABLY HEREDITARY, CHARACTERISED BY SEVERE MENTAL DEFICIENCY AND A CONSTANT GROSS ABNORMALITY OF AMINOACID METABOLISMThe Lancet, 1958