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5. Inborn errors of urea synthesis. Batshaw ML. Ann Neurol; 1994 Feb; 35(2):133-41. PubMed ID: 7906500 [Abstract] [Full Text] [Related]
6. Urea cycle disorders: clinical presentation outside the newborn period. Smith W, Kishnani PS, Lee B, Singh RH, Rhead WJ, Sniderman King L, Smith M, Summar M. Crit Care Clin; 2005 Oct; 21(4 Suppl):S9-17. PubMed ID: 16227115 [Abstract] [Full Text] [Related]
7. Survival after treatment with phenylacetate and benzoate for urea-cycle disorders. Enns GM, Berry SA, Berry GT, Rhead WJ, Brusilow SW, Hamosh A. N Engl J Med; 2007 May 31; 356(22):2282-92. PubMed ID: 17538087 [Abstract] [Full Text] [Related]
8. 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 04; 288(1):1-6. PubMed ID: 4681895 [No Abstract] [Full Text] [Related]
9. Diagnosis of urea cycle disorders. Bachmann C. Enzyme; 1987 Jan 04; 38(1-4):233-41. PubMed ID: 3440447 [Abstract] [Full Text] [Related]
10. Ammonia toxicity and its prevention in inherited defects of the urea cycle. Walker V. Diabetes Obes Metab; 2009 Sep 04; 11(9):823-35. PubMed ID: 19531057 [Abstract] [Full Text] [Related]
11. [Hyperammonemia type II as an example of urea cycle disorder]. Hawrot-Kawecka AM, Kawecki GP, Duława J. Wiad Lek; 2006 Sep 04; 59(7-8):512-5. PubMed ID: 17209350 [Abstract] [Full Text] [Related]
12. Hyperammonemia in lysinuric protein intolerance. Kato T, Mizutani N, Ban M. Pediatrics; 1984 Apr 04; 73(4):489-92. PubMed ID: 6424086 [Abstract] [Full Text] [Related]
13. [Neonatal hyperammonemia]. Jaeken J, Devlieger H, Evens M, Casaer P, Eggermont E. Tijdschr Kindergeneeskd; 1983 Jun 04; 51(3):101-4. PubMed ID: 6636106 [Abstract] [Full Text] [Related]
14. Clinical aspects of disorders of the urea cycle. Snyderman SE. Pediatrics; 1981 Aug 04; 68(2):284-9, 295-7. PubMed ID: 7267239 [No Abstract] [Full Text] [Related]
15. Focal glycogenosis of the liver in disorders of ureagenesis: its occurrence and diagnostic significance. Badizadegan K, Perez-Atayde AR. Hepatology; 1997 Aug 04; 26(2):365-73. PubMed ID: 9252147 [Abstract] [Full Text] [Related]
17. Blood levels of ammonia and nitrogen scavenging amino acids in patients with inherited hyperammonemia. Tuchman M, Yudkoff M. Mol Genet Metab; 1999 Jan 04; 66(1):10-5. PubMed ID: 9973542 [Abstract] [Full Text] [Related]
18. Urea cycle disorders in Thai infants: a report of 5 cases. Wasant P, Srisomsap C, Liammongkolkul S, Svasti J. J Med Assoc Thai; 2002 Aug 04; 85 Suppl 2():S720-31. PubMed ID: 12403252 [Abstract] [Full Text] [Related]
19. Waste nitrogen excretion via amino acid acylation: benzoate and phenylacetate in lysinuric protein intolerance. Simell O, Sipilä I, Rajantie J, Valle DL, Brusilow SW. Pediatr Res; 1986 Nov 04; 20(11):1117-21. PubMed ID: 3099249 [Abstract] [Full Text] [Related]
20. Inborn errors of the urea cycle. Walter JH, Leonard JV. Br J Hosp Med; 1987 Sep 04; 38(3):176-83. PubMed ID: 3315071 [Abstract] [Full Text] [Related] Page: [Next] [New Search]