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6. Use of citrulline as a diagnostic marker in the prospective treatment of urea cycle disorders. Batshaw ML; Berry GT J Pediatr; 1991 Jun; 118(6):914-7. PubMed ID: 2040929 [No Abstract] [Full Text] [Related]
7. Proceedings of a satellite meeting on advances in inherited urea cycle disorders. Vienna, 20-21 May 1997. J Inherit Metab Dis; 1998; 21 Suppl 1():1-159. PubMed ID: 9686340 [No Abstract] [Full Text] [Related]
12. [Hyperammonemias of childhood. I. Enzymopathies of the urea cycle]. Kopieczna-Grzebieniak E; Toborek M; Tarnawski R; Jakubowska D Pediatr Pol; 1987 Oct; 62(10):727-32. PubMed ID: 3328149 [No Abstract] [Full Text] [Related]
13. Proceedings: Hepatic ultrastructure in a child with carbamyl phosphate synthetase deficiency, hyperornithinaemia, hyperammonaemia, and homocitrullinuria. Haust MD; Gatfield PD Arch Dis Child; 1975 Aug; 50(8):663. PubMed ID: 173245 [No Abstract] [Full Text] [Related]
14. Auxiliary liver transplantation for urea-cycle enzyme deficiencies: lessons from three cases. Kiuchi T; Edamoto Y; Kaibori M; Uryuhara K; Kasahara M; Uemoto S; Egawa H; Inomata Y; Tanaka K Transplant Proc; 1999; 31(1-2):528-9. PubMed ID: 10083221 [No Abstract] [Full Text] [Related]
15. Developmental outcomes with early orthotopic liver transplantation for infants with neonatal-onset urea cycle defects and a female patient with late-onset ornithine transcarbamylase deficiency. McBride KL; Miller G; Carter S; Karpen S; Goss J; Lee B Pediatrics; 2004 Oct; 114(4):e523-6. PubMed ID: 15466081 [TBL] [Abstract][Full Text] [Related]