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27. Urinary purines and pyrimidines in patients with hyperammonemia of various origins. Van Gennip AH; Van Bree-Blom EJ; Grift J; DeBree PK; Wadman SK Clin Chim Acta; 1980 Jun; 104(2):227-39. PubMed ID: 6771064 [TBL] [Abstract][Full Text] [Related]
28. 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]
29. Hyperammonemia: the silent killer. Miga DE; Roth KS South Med J; 1993 Jul; 86(7):742-7. PubMed ID: 8322080 [TBL] [Abstract][Full Text] [Related]
30. Genetic variation in the urea cycle: a model resource for investigating key candidate genes for common diseases. Mitchell S; Ellingson C; Coyne T; Hall L; Neill M; Christian N; Higham C; Dobrowolski SF; Tuchman M; Summar M; Hum Mutat; 2009 Jan; 30(1):56-60. PubMed ID: 18666241 [TBL] [Abstract][Full Text] [Related]
31. [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]
32. Urea cycle disorders: clinical presentation outside the newborn period. Smith W; Kishnani PS; Lee B; Singh RH; Rhead WJ; Sniderman King L; Smith M; Summar M Crit Care Clin; 2005 Oct; 21(4 Suppl):S9-17. PubMed ID: 16227115 [TBL] [Abstract][Full Text] [Related]
33. Survival after treatment with phenylacetate and benzoate for urea-cycle disorders. Enns GM; Berry SA; Berry GT; Rhead WJ; Brusilow SW; Hamosh A N Engl J Med; 2007 May; 356(22):2282-92. PubMed ID: 17538087 [TBL] [Abstract][Full Text] [Related]
34. [Pulmonary hemorrhages in newborn infants with inborn errors of the 1st 2 phases of the urea cycle]. Plöchl E; Bachmann C Monatsschr Kinderheilkd; 1983 Oct; 131(10):714-5. PubMed ID: 6646142 [TBL] [Abstract][Full Text] [Related]
35. 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]
36. 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]
37. [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]