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5. [Prenatal diagnosis of enzymopathies of the urea cycle]. Chadefaux B; Rabier D; Kamoun P Ann Biol Clin (Paris); 1988; 46(7):471-6. PubMed ID: 3056128 [TBL] [Abstract][Full Text] [Related]
6. Double deficiencies of urea cycle enzymes in human liver. Raijman L Biochem Med; 1979 Apr; 21(2):226-33. PubMed ID: 465019 [No Abstract] [Full Text] [Related]
7. [Molecular genetics of urea cycle diseases]. Ohtake A; Mori M Seikagaku; 1990 Sep; 62(9):1170-7. PubMed ID: 2258657 [No Abstract] [Full Text] [Related]
8. 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]
17. [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]
18. [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]
19. Detection of urea cycle enzymopathies in childhood. Trauner DA; Self TW Arch Neurol; 1984 Jul; 41(7):758-60. PubMed ID: 6743067 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]