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.
3. Familial protein intolerance. Possible nature of enzyme defect. Malmquist J; Jagenburg R; Lindstedt G N Engl J Med; 1971 May; 284(18):997-1002. PubMed ID: 5553484 [No Abstract] [Full Text] [Related]
4. [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]
5. The sparse fur mouse: an animal model for a human inborn error of metabolism of the urea cycle. Spector EB; Mazzocchi RA Prog Clin Biol Res; 1983; 127():85-96. PubMed ID: 6889405 [No Abstract] [Full Text] [Related]
6. [Inborn metabolic errors due to disorders in the urea synthesis cycle]. Kardosová A; Hruskovic I; Strnová J Cesk Pediatr; 1986 Jan; 41(1):31-3. PubMed ID: 3948272 [No Abstract] [Full Text] [Related]
7. Clinical aspects of disorders of the urea cycle. Snyderman SE Pediatrics; 1981 Aug; 68(2):284-9, 295-7. PubMed ID: 7267239 [No Abstract] [Full Text] [Related]
8. Inborn errors of urea synthesis. Batshaw ML Ann Neurol; 1994 Feb; 35(2):133-41. PubMed ID: 7906500 [TBL] [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]