Author:
Leonard J.V.,Morris A.A.M.
Subject
Pediatrics, Perinatology and Child Health
Reference22 articles.
1. Ornithine aminotransferase deficiency presenting with hyperammonaemia in a premature newborn;Webster;J Inherit Metab Dis,1999
2. Ornithine aminotransferase deficiency: difficulties in diagnosis in the neonatal period;Cleary;J Inherit Metab Dis,1999
3. Differentiation of transient hyperammonaemia of the newborn and urea cycle enzyme defects by clinical presentation;Hudak;J Pediatr,1985
4. Use of citrulline as a diagnostic marker in the prospective treatment of urea cycle disorders;Batshaw;J Pediatr,1991
5. Therapeutic use of carbamylglutamate in the case of carbamoyl-phosphate synthetase deficiency;Kuchler;J Inherit Metab Dis,1996
Cited by
133 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献