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5. [Hereditary hyperammonemia due to qualitative abnormality of hepatic and intestinal ornithine carbamoyl-transferase]. Cathelineau L; Navarro J; Aymard P; Baudon JJ; Mondet Y; Polonovski C; Laplane R Arch Fr Pediatr; 1972; 29(7):713-36. PubMed ID: 4644461 [No Abstract] [Full Text] [Related]
6. Hyperammonemia due to a mutant enzyme of ornithine transcarbamylase. Matsuda I; Arashima S; Nambu H; Takekoshi Y; Anakura M Pediatrics; 1971 Oct; 48(4):595-600. PubMed ID: 5114747 [No Abstract] [Full Text] [Related]
7. The congenital hyperammonemic syndrome. Berenberg W; Kang ES Dev Med Child Neurol; 1971 Jun; 13(3):355-61. PubMed ID: 5093296 [No Abstract] [Full Text] [Related]
8. Periodic attacks of lethargy in a baby with ammonia intoxication due to a congenital defect in ureogenesis. Corbeel LM; Colombo JP; Van Sande M; Weber A Arch Dis Child; 1969 Dec; 44(238):681-7. PubMed ID: 5356973 [No Abstract] [Full Text] [Related]
9. Ornithine transcarbamylase deficiency: a cause of lethal neonatal hyperammonemia in males. Campbell AG; Rosenberg LE; Snodgrass PJ; Nuzum CT N Engl J Med; 1973 Jan; 288(1):1-6. PubMed ID: 4681895 [No Abstract] [Full Text] [Related]
10. New pathways of nitrogen excretion in inborn errors of urea synthesis. Brusilow SW; Valle DL; Batshaw M Lancet; 1979 Sep; 2(8140):452-4. PubMed ID: 89510 [TBL] [Abstract][Full Text] [Related]
11. [Hyperammonemia--congenital abnormality of the urea cycle]. Arashima I Saishin Igaku; 1972 Apr; 27(4):730-42. PubMed ID: 5026635 [No Abstract] [Full Text] [Related]
13. Ornithine transcarbamylase deficiency in the newborn infant. Kang ES; Snodgrass PJ; Gerald PS J Pediatr; 1973 Apr; 82(4):642-9. PubMed ID: 4698340 [No Abstract] [Full Text] [Related]
14. Metabolic and genetic studies of a family with ornithine transcarbamylase deficiency. Goldstein AS; Hoogenraad NJ; Johnson JD; Fukanaga K; Swierczewski E; Cann HM; Sunshine P Pediatr Res; 1974 Jan; 8(1):5-12. PubMed ID: 4809308 [No Abstract] [Full Text] [Related]
15. Hyperammonemia due to a defect in hepatic ornithine transcarbamylase. Sunshine P; Lindenbaum JE; Levy HL; Freeman JM Pediatrics; 1972 Jul; 50(1):100-11. PubMed ID: 5038084 [No Abstract] [Full Text] [Related]
16. [Congenital hyperammoniemia caused by ornithine carbamoyl-transferase and carbamyl phosphate synthetase deficiency]. Salle B; Levin B; Longin B; Richard P; Andre M; Gauthier J Arch Fr Pediatr; 1972 May; 29(5):493-504. PubMed ID: 4655647 [No Abstract] [Full Text] [Related]
17. [Constitutional hyperammonemia with carbamoylphosphate synthetase deficiency. Course treatment during dietetic]. Odievre M; Charpentier C; Cathelineau L; Vedrenne J; Delacoux des Roseaux F; Mercie C Arch Fr Pediatr; 1973 Jan; 30(1):5-13. PubMed ID: 4721588 [No Abstract] [Full Text] [Related]
18. Decreased hyperammonaemia and orotic aciduria due to inactivation of ornithine aminotransferase in mice with a hereditary abnormal ornithine carbamoyltransferase. Seiler N; Grauffel C; Daune-Anglard G; Sarhan S; Knödgen B J Inherit Metab Dis; 1994; 17(6):691-703. PubMed ID: 7707692 [TBL] [Abstract][Full Text] [Related]
19. Inborn errors of urea synthesis. Batshaw ML Ann Neurol; 1994 Feb; 35(2):133-41. PubMed ID: 7906500 [TBL] [Abstract][Full Text] [Related]
20. Hyperammonaemia in 20 families. Biochemical and genetical survey, including investigations in 3 new families. Palmer T; Oberholzer VG; Burgess EA; Butler LJ; Levin B Arch Dis Child; 1974 Jun; 49(6):443-9. PubMed ID: 4852321 [No Abstract] [Full Text] [Related] [Next] [New Search]