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2. Urea biosynthesis II. Normal and abnormal regulation. Shambaugh GE Am J Clin Nutr; 1978 Jan; 31(1):126-33. PubMed ID: 339704 [No Abstract] [Full Text] [Related]
12. Inborn defects of the mitochondrial portion of the urea cycle. Colombo JP; Bachmann C; Schrämmli A Ann N Y Acad Sci; 1986; 488():109-17. PubMed ID: 3555250 [No Abstract] [Full Text] [Related]
16. Contrasting features of urea cycle disorders in human patients and knockout mouse models. Deignan JL; Cederbaum SD; Grody WW Mol Genet Metab; 2008 Jan; 93(1):7-14. PubMed ID: 17933574 [TBL] [Abstract][Full Text] [Related]
17. Arginine, an indispensable amino acid for patients with inborn errors of urea synthesis. Brusilow SW J Clin Invest; 1984 Dec; 74(6):2144-8. PubMed ID: 6511918 [TBL] [Abstract][Full Text] [Related]
18. Definitive cure of hyperammonemia by liver transplantation in urea cycle defects: report of three cases. Jan D; Poggi F; Jouvet P; Rabier D; Laurent J; Beringer A; Hubert P; Saudubray JM; Revillon Y Transplant Proc; 1994 Feb; 26(1):188. PubMed ID: 8108934 [No Abstract] [Full Text] [Related]
19. 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]
20. [Hereditary diseases related to a disorder of the enzymatic activity of the urea formation cycle]. Kazanskaia NS; Alekseenko LP Vopr Med Khim; 1976; 22(4):435-43. PubMed ID: 800301 [No Abstract] [Full Text] [Related] [Next] [New Search]