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26. [Comments on the contribution, Therapy of hyperammonemia in carbamylphosphate synthetase deficiency with peritoneal dialysis and venovenous hemofiltration, by B. Lettgen et al]. Brockstedt M Monatsschr Kinderheilkd; 1992 Jul; 140(7):431. PubMed ID: 1308100 [No Abstract] [Full Text] [Related]
27. Dysautonomia in an infant with secondary hyperammonemia due to propionyl coenzyme A carboxylase deficiency. Harris DJ; Yang BI; Wolf B; Snodgrass PJ Pediatrics; 1980 Jan; 65(1):107-10. PubMed ID: 7355003 [TBL] [Abstract][Full Text] [Related]
29. 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]
30. Molecular genetic research into carbamoyl-phosphate synthase I: molecular defects and linkage markers. Summar ML J Inherit Metab Dis; 1998; 21 Suppl 1():30-9. PubMed ID: 9686343 [TBL] [Abstract][Full Text] [Related]
31. Survival after early treatment for carbamyl phosphate synthetase (CPS) I deficiency associated with increase of intramitochondrial CPS I. Zimmer KP; Naim HY; Koch HG; Colombo JP; Rossi R; Schmid KW; Deufel T; Ullrich K; Harms E Lancet; 1995 Dec; 346(8989):1530-1. PubMed ID: 7491050 [TBL] [Abstract][Full Text] [Related]
32. Liver ultrastructure in mitochondrial urea cycle enzyme deficiencies and comparison with Reye's syndrome. Latham PS; LaBrecque DR; McReynolds JW; Klatskin G Hepatology; 1984; 4(3):404-7. PubMed ID: 6724509 [TBL] [Abstract][Full Text] [Related]
33. Carbamyl phosphate synthetase-1 deficiency discovered after valproic acid-induced coma. Verbiest HB; Straver JS; Colombo JP; van der Vijver JC; van Woerkom TC Acta Neurol Scand; 1992 Sep; 86(3):275-9. PubMed ID: 1414247 [TBL] [Abstract][Full Text] [Related]
34. Carbamyl phosphate synthetase I deficiency with no detectable mRNA activity. Suzuki Y; Matsushima A; Ohtake A; Mori M; Tatibana M; Orii T Eur J Pediatr; 1986 Oct; 145(5):406-8. PubMed ID: 3792387 [TBL] [Abstract][Full Text] [Related]
35. The activity of carbamoyl-phosphate synthetase I and ornithine carbamoyltransferase (OCT) in the intestine and screening for OCT deficiency in the rectal mucosa. Matsushima A; Orii T J Inherit Metab Dis; 1981; 4(2):83-4. PubMed ID: 6790859 [No Abstract] [Full Text] [Related]
36. Arginine deficiency syndrome. Its occurrence in carbamyl phosphate synthetase deficiency. Kline JJ; Hug G; Schubert WK; Berry H Am J Dis Child; 1981 May; 135(5):437-42. PubMed ID: 7234771 [TBL] [Abstract][Full Text] [Related]
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39. 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]
40. 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] [Previous] [Next] [New Search]