Partial ornithine transcarbamylase deficiency simulating Reye syndrome
- 31 December 1981
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 99 (6) , 929-931
- https://doi.org/10.1016/s0022-3476(81)80025-x
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
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- Ornithine transcarbamylase deficiency in a boy with normal developmentThe Journal of Pediatrics, 1980
- Atypical Clinical Course of Ornithine Transcarbamyiase Deficiency Due to a New Mutant (Comparison with Reye's Disease)Journal of Clinical Endocrinology & Metabolism, 1979
- Some kinetic properties of liver ornithine carbamoyl transferase (oct) in a patient with oct deficiencyClinica Chimica Acta; International Journal of Clinical Chemistry, 1977
- A direct method for the estimation of ornithine carbamoyltransferase activity in serumClinica Chimica Acta; International Journal of Clinical Chemistry, 1976
- HEREDITARY ORNITHINE TRANSCARBAMYLASE DEFICIENCYActa Paediatrica, 1975
- Evidence for X-Linked Dominant Inheritance of Ornithine Transcarbamylase DeficiencyNew England Journal of Medicine, 1973
- Hyperammonaemia. A variant type of deficiency of liver ornithine transcarbamylase.Archives of Disease in Childhood, 1969
- A COLORIMETRIC DETERMINATION OF OROTIC ACIDTHE JOURNAL OF VITAMINOLOGY, 1963