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27. [Cerebral edema with hyperammonemia in valpromide poisoning. Manifestation in an adult, of a partial deficit in type I carbamylphosphate synthetase]. Bourrier P; Varache N; Alquier P; Rabier D; Kamoun P; Lorre G; Alhayek G Presse Med; 1988 Nov; 17(39):2063-6. PubMed ID: 2974563 [TBL] [Abstract][Full Text] [Related]
29. [Carbamyl phosphate synthase deficiency: clinical symptoms, diagnosis and dietary-medicamentous treatment in the neonatal period and infancy]. Hochreutener H; Issakainen J; Bachmann C; Baerlocher K Helv Paediatr Acta; 1989 Jun; 43(5-6):493-505. PubMed ID: 2745145 [TBL] [Abstract][Full Text] [Related]
30. Transiently reduced activity of carbamyl phosphate synthetase and ornithine transcarbamylase in liver of children with Reye's syndrome. Brown T; Hug G; Lansky L; Bove K; Scheve A; Ryan M; Brown H; Schubert WK; Partin JC; Lloyd-Still J N Engl J Med; 1976 Apr; 294(16):861-7. PubMed ID: 175276 [TBL] [Abstract][Full Text] [Related]
32. Postpartum coma and death due to carbamoyl-phosphate synthetase I deficiency. Wong LJ; Craigen WJ; O'Brien WE Ann Intern Med; 1994 Feb; 120(3):216-7. PubMed ID: 8273985 [No Abstract] [Full Text] [Related]
33. A case of carbamylphosphate synthetase-I deficiency associated with secondary carnitine deficiency--L-carnitine treatment of CPS-I deficiency. Mori T; Tsuchiyama A; Nagai K; Nagao M; Oyanagi K; Tsugawa S Eur J Pediatr; 1990 Jan; 149(4):272-4. PubMed ID: 2303075 [TBL] [Abstract][Full Text] [Related]
34. [Carbamyl phosphate synthetase I deficiency]. Ohtake A; Mori M Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):497-9. PubMed ID: 3270854 [No Abstract] [Full Text] [Related]
35. Mice deficient in the urea-cycle enzyme, carbamoyl phosphate synthetase I, die during the early neonatal period from hyperammonemia. Schofield JP; Cox TM; Caskey CT; Wakamiya M Hepatology; 1999 Jan; 29(1):181-5. PubMed ID: 9862865 [TBL] [Abstract][Full Text] [Related]
36. Quantitative analysis of urinary pyroglutamic acid in patients with hyperammonemia. Nakanishi T; Shimizu A; Saiki K; Fujiwara F; Funahashi S; Hayashi A Clin Chim Acta; 1991 Mar; 197(3):249-55. PubMed ID: 2049866 [No Abstract] [Full Text] [Related]
37. Carbamylphosphate synthetase-I deficiency in a newborn: survival after early diagnosis and therapy. Raghavan K; Chabra S; Mondkar J; Aiyar R; Ambani LM; Fernandez A Indian Pediatr; 1991 May; 28(5):551-4. PubMed ID: 1752685 [No Abstract] [Full Text] [Related]
38. 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]
39. 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]
40. Cloning and sequence of a cDNA encoding human carbamyl phosphate synthetase I: molecular analysis of hyperammonemia. Haraguchi Y; Uchino T; Takiguchi M; Endo F; Mori M; Matsuda I Gene; 1991 Nov; 107(2):335-40. PubMed ID: 1840546 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]