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9. Plasma alpha-ketoglutarate in urea cycle enzymopathies and its role as a harbinger of hyperammonemic coma. Batshaw ML; Walser M; Brusilow SW Pediatr Res; 1980 Dec; 14(12):1316-9. PubMed ID: 7208146 [TBL] [Abstract][Full Text] [Related]
10. Treatment of inborn errors of urea synthesis: activation of alternative pathways of waste nitrogen synthesis and excretion. Batshaw ML; Brusilow S; Waber L; Blom W; Brubakk AM; Burton BK; Cann HM; Kerr D; Mamunes P; Matalon R; Myerberg D; Schafer IA N Engl J Med; 1982 Jun; 306(23):1387-92. PubMed ID: 7078580 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. [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]
13. [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]
14. Editorial: Ammonia disposal in Reye's syndrome. Smith AL N Engl J Med; 1976 Apr; 294(16):897-8. PubMed ID: 1250317 [No Abstract] [Full Text] [Related]
15. Hereditary disorders of the urea cycle in man: biochemical and molecular approaches. Saheki T; Kobayashi K; Inoue I Rev Physiol Biochem Pharmacol; 1987; 108():21-68. PubMed ID: 3306877 [No Abstract] [Full Text] [Related]
16. 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]