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.
353 related articles for article (PubMed ID: 5038084)
1. 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]
2. 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]
3. 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]
4. Hyperornithinemia, hyperammonemia, and homocitrullinuria. A new disorder of amino acid metabolism associated with myoclonic seizures and mental retardation. Shih VE; Efron ML; Moser HW Am J Dis Child; 1969 Jan; 117(1):83-92. PubMed ID: 5782534 [No Abstract] [Full Text] [Related]
5. Evidence for x-linked dominant inheritance of ornithine transcarbamylase deficiency. Short EM; Conn HO; Snodgrass PJ; Campbell AG; Rosenberg LE N Engl J Med; 1973 Jan; 288(1):7-12. PubMed ID: 4681915 [No Abstract] [Full Text] [Related]
6. 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]
7. [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]
8. Study of enzyme defect in a case of ornithine transcarbamylase deficiency. Qureshi IA; Letarte J; Quellet R Diabete Metab; 1978 Dec; 4(4):239-41. PubMed ID: 729890 [TBL] [Abstract][Full Text] [Related]
9. Ornithine transcarbamylase deficiency in male adolescence and adulthood. Yoshino M; Nishiyori J; Yamashita F; Kumashiro R; Abe H; Tanikawa K; Ohno T; Nakao K; Kaku N; Fukushima H Enzyme; 1990; 43(3):160-8. PubMed ID: 2095337 [TBL] [Abstract][Full Text] [Related]
10. [A new family with mutation of the structural gene of human ornithine carbamoyltransferase]. Stoll C; Bieth R; Dreyfus J; Flori E; Lutz P; Levy JM Arch Fr Pediatr; 1978 May; 35(5):512-8. PubMed ID: 678030 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Spontaneous animal models of ornithine transcarbamylase deficiency: studies on serum and urinary nitrogenous metabolites. Qureshi IA; Letarte J; Ouellet R Adv Exp Med Biol; 1982; 153():173-83. PubMed ID: 7164896 [No Abstract] [Full Text] [Related]
14. Hyperammonaemia: a deficiency of liver ornithine transcarbamylase. Occurrence in mother and child. Levin B; Abraham JM; Oberholzer VG; Burgess EA Arch Dis Child; 1969 Apr; 44(234):152-61. PubMed ID: 5779426 [No Abstract] [Full Text] [Related]
17. Ornithine transcarbamylase deficiency--a cause of bizarre behavior in a man. DiMagno EP; Lowe JE; Snodgrass PJ; Jones JD N Engl J Med; 1986 Sep; 315(12):744-7. PubMed ID: 3748082 [No Abstract] [Full Text] [Related]
18. Partial ornithine carbamyl transferase deficiency: an inborn error of the urea cycle presenting as orotic aciduria in a male infant. MacLeod P; Mackenzie S; Scriver CR Can Med Assoc J; 1972 Sep; 107(5):405-8. PubMed ID: 5074751 [TBL] [Abstract][Full Text] [Related]
19. [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]