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6. 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]
7. Citrullinaemia with rapidly fatal neonatal course. Van Der Zee SP; Trijbels JM; Monnens LA; Hommes FA; Schretlen ED Arch Dis Child; 1971 Dec; 46(250):847-51. PubMed ID: 5129187 [TBL] [Abstract][Full Text] [Related]
8. Studies on amino acid metabolism in citrullinuria. Mohyuddin F; Rathbun JC; McMurray WC Am J Dis Child; 1967 Jan; 113(1):152-6. PubMed ID: 6015893 [No Abstract] [Full Text] [Related]
9. Nitrogen metabolism in neonatal citrullinaemia. Walser M; Batshaw M; Sherwood G; Robinson B; Brusilow S Clin Sci Mol Med; 1977 Aug; 53(2):173-81. PubMed ID: 891106 [No Abstract] [Full Text] [Related]
10. Continuous arteriovenous haemofiltration in a neonate with hyperammonaemic coma due to citrullinaemia. Sperl W; Geiger R; Maurer H; Murr C; Schmoigl C; Steichen-Gersdorf E; Sailer M J Inherit Metab Dis; 1992; 15(1):158-9. PubMed ID: 1583872 [No Abstract] [Full Text] [Related]
11. Use of citrulline as a diagnostic marker in the prospective treatment of urea cycle disorders. Batshaw ML; Berry GT J Pediatr; 1991 Jun; 118(6):914-7. PubMed ID: 2040929 [No Abstract] [Full Text] [Related]
12. A case of transient neonatal citrullinemia. Ohtake A; Takayanagi M; Ogura N; Nakajima H Eur J Pediatr; 1983 Oct; 141(1):60-1. PubMed ID: 6641770 [TBL] [Abstract][Full Text] [Related]
13. [A patient with neonatal citrullinemia]. Berghuis M; Cats BP; de Klerk JB; Duran M Tijdschr Kindergeneeskd; 1983 Jun; 51(3):104-9. PubMed ID: 6636107 [TBL] [Abstract][Full Text] [Related]
16. Evaluation of gene therapy for citrullinaemia using murine and bovine models. Patejunas G; Lee B; Dennis JA; Healy PJ; Reeds PJ; Yu H; Frazer M; Mull B; Warman AW; Beaudet AL; O'Brien WE J Inherit Metab Dis; 1998; 21 Suppl 1():138-50. PubMed ID: 9686351 [TBL] [Abstract][Full Text] [Related]
17. [Severe neonatal type of citrullinemia. Difficulties to expose heterozygotic state. Advantage of prenatal diagnosis (author's transl)]. Plasse M; Serre JC; Joannard A; Favier A; Grandgeorges D; Frappat P; Bost M Ann Pediatr (Paris); 1980 Oct; 27(8):491-6. PubMed ID: 7235517 [No Abstract] [Full Text] [Related]
18. New approaches to the diagnosis and treatment of inborn errors or urea synthesis. Batshaw ML; Thomas GH; Brusilow SW Pediatrics; 1981 Aug; 68(2):290-7. PubMed ID: 7267240 [No Abstract] [Full Text] [Related]
19. Serum arginine level in neonatal citrullinaemia. Matsoo M; Takemine H; Aida M; Nakamura H; Matsuo T J Inherit Metab Dis; 1988; 11(3):309-10. PubMed ID: 3148076 [No Abstract] [Full Text] [Related]
20. Ornithine aminotransferase deficiency: diagnostic difficulties in neonatal presentation. Cleary MA; Dorland L; de Koning TJ; Poll-The BT; Duran M; Mandell R; Shih VE; Berger R; Olpin SE; Besley GT J Inherit Metab Dis; 2005; 28(5):673-9. PubMed ID: 16151897 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]