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23. [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]
24. 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]
25. Ornithine transcarbamylase, an isoelectric point (pI) isozyme in human liver and its deficiency. Arashima S; Matsuda I Biochem Biophys Res Commun; 1971 Oct; 45(1):145-50. PubMed ID: 5139917 [No Abstract] [Full Text] [Related]
29. Ornithine transcarbamylase deficiency in mutant mice I. Studies on the characterization of enzyme defect and suitability as animal model of human disease. Qureshi IA; Letarte J; Ouellet R Pediatr Res; 1979 Jul; 13(7):807-11. PubMed ID: 481951 [No Abstract] [Full Text] [Related]
30. [DNA diagnosis of ornithine transcarbamylase deficiency by PCR method]. Matsuura T; Matsuda I Tanpakushitsu Kakusan Koso; 1990 Dec; 35(17):3113-9. PubMed ID: 2287729 [No Abstract] [Full Text] [Related]
31. The implications of hyperammonemia in rare and common disorders, including migraine. Russell A Mt Sinai J Med; 1973; 40(5):609-30. PubMed ID: 4542418 [No Abstract] [Full Text] [Related]
32. [Ornithine transcarbamylase deficiency]. Hata A Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):500-4. PubMed ID: 2908395 [No Abstract] [Full Text] [Related]
33. Hyperammonemia caused by impaired mitochondrial ornithine transport in a patient with partial quantitative deficiency of ornithine carbamoyltransferase. Kuno T; Miyazaki S; Inoue I; Saheki T Clin Biochem; 1990 Apr; 23(2):143-7. PubMed ID: 2372929 [TBL] [Abstract][Full Text] [Related]
34. Metabolite distribution in cells. Davis RH Science; 1972 Nov; 178(4063):835-40. PubMed ID: 5085981 [No Abstract] [Full Text] [Related]
35. Kinetic analysis of a new human ornithine carbamoyltransferase variant. Cathelineau L; Briand P; Petit F; Nuyts JP; Farriaux JP; Kamoun PP Biochim Biophys Acta; 1980 Jul; 614(1):40-5. PubMed ID: 7397202 [TBL] [Abstract][Full Text] [Related]
36. Partial duplication [dup. TCAC (178)] and novel point mutations (T125M, G188R, A209V, and H302L) of the ornithine transcarbamylase gene in congenital hyperammonemia. Gilbert-Dussardier B; Segues B; Rozet JM; Rabier D; Calvas P; de Lumley L; Bonnefond JP; Munnich A Hum Mutat; 1996; 8(1):74-6. PubMed ID: 8807340 [No Abstract] [Full Text] [Related]
37. Peritoneal clearance of ammonia and creatinine in a neonate. Siegel NJ; Brown RS J Pediatr; 1973 Jun; 82(6):1044-6. PubMed ID: 4702897 [No Abstract] [Full Text] [Related]
38. Qualitative abnormality of liver argininosuccinate synthetase in a patient with citrullinemia. Matsuda Y; Tsuji A; Katunuma N Adv Exp Med Biol; 1982; 153():77-82. PubMed ID: 7164924 [No Abstract] [Full Text] [Related]
39. [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]
40. Ornithine carbamoyltransferase deficiency. A new variant with subnormal enzyme activity. Rabier D; Benoit A; Petit F; Chekoury A; Bonnefont JP; Saudubray JM; Kamoun P Clin Chim Acta; 1989 Dec; 186(1):25-9. PubMed ID: 2612006 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]