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6. [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]
7. [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]
8. [Hereditary ornithine-carbamyl-transferase deficiency with qualitative enzyme abnormality. Report of a form with neonatal revelation and fatal course in a boy]. Saudubray JM; Cathelineau L; Charpentier C; Boisse J; Allaneau C; Le Bont H; Lesage B Arch Fr Pediatr; 1973 Jan; 30(1):15-27. PubMed ID: 4721585 [No Abstract] [Full Text] [Related]
9. Treatment of carbamyl phosphate synthetase deficiency with keto analogues of essential amino acids. Batshaw M; Brusilow S; Walser M N Engl J Med; 1975 May; 292(21):1085-90. PubMed ID: 165404 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. Citrullinemia: a new case, with implications concerning adaptation to defective urea synthesis. Scott-Emuakpor A; Higgins JV; Kohrman AF Pediatr Res; 1972 Jul; 6(7):626-33. PubMed ID: 5057291 [No Abstract] [Full Text] [Related]
15. Blood levels of ammonia and nitrogen scavenging amino acids in patients with inherited hyperammonemia. Tuchman M; Yudkoff M Mol Genet Metab; 1999 Jan; 66(1):10-5. PubMed ID: 9973542 [TBL] [Abstract][Full Text] [Related]
16. Ornithine transcarbamylase deficiency: case report and review. Bueno JD; Lutz R; Cho S Kans Med; 1995; 96(3):135-8. PubMed ID: 8583741 [No Abstract] [Full Text] [Related]
17. Congenital disorders of the urea cycle and ammonia detoxication. Colombo JP Monogr Paediatr; 1971; 1():1-150. PubMed ID: 4946766 [No Abstract] [Full Text] [Related]
18. [Neonatal hyperammonemia due to ornithine transcarbamylase deficiency (author's transl)]. del Valle JA; Urbón A; García MJ; Cuadrado P; Ugarte M An Esp Pediatr; 1982 May; 16(5):416-20. PubMed ID: 7114619 [TBL] [Abstract][Full Text] [Related]
19. A case of carbamyl phosphate synthetase deficiency. Arashima S; Matsuda I Tohoku J Exp Med; 1972 Jun; 107(2):143-7. PubMed ID: 4641111 [No Abstract] [Full Text] [Related]