These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
6. [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]
7. Immunological evidence for a carbamylphosphate synthetase lesion resulting in the formation of enzyme with altered sub-unit size. Hoogenraad NJ; Weston HJ; Mackenzie N J Inherit Metab Dis; 1986; 9(4):367-73. PubMed ID: 3104674 [TBL] [Abstract][Full Text] [Related]
8. Autosomal recessive inheritance of human mitochondrial carbamyl phosphate synthetase deficiency. McReynolds JW; Crowley B; Mahoney MJ; Rosenberg LE Am J Hum Genet; 1981 May; 33(3):345-53. PubMed ID: 7246541 [TBL] [Abstract][Full Text] [Related]
9. Identification of benzoylcarnitine in the urine of a patient of hyperammonemia. Sakuma T; Asai K; Ichiki T; Sugiyama N; Kidouchi K; Wada Y Tohoku J Exp Med; 1989 Oct; 159(2):147-51. PubMed ID: 2609332 [TBL] [Abstract][Full Text] [Related]
10. [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]
15. Hyperammonemia related to carnitine metabolism with particular emphasis on ornithine transcarbamylase deficiency. Matsuda I; Ohtani Y; Ohyanagi K; Yamamoto S Enzyme; 1987; 38(1-4):251-5. PubMed ID: 3440448 [TBL] [Abstract][Full Text] [Related]
16. Severe neonatal deficiency of carbamylphosphate synthetase. Lambotte C; Adam A; Van Der Hofstadt J; Dodinval-Versie J; Gielen J Acta Paediatr Belg; 1977; 30(3):151-5. PubMed ID: 204150 [No Abstract] [Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. A lethal neonatal variant of carbamoyl-phosphate synthetase deficiency in combination with an intermediate activity of L-ornithine: 2-oxoglutarate amino-transferase. van der Heiden C; Beemer FA; van Dijk HA; Desplanque J; Gerards LJ Clin Genet; 1983 May; 23(5):363-8. PubMed ID: 6851228 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]