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3. Case report: recurrent hyperammonaemic encephalopathy due to citrullinaemia in a 52 year old man. Chow WC; Ng HS; Tan IK; Thum TY J Gastroenterol Hepatol; 1996 Jul; 11(7):621-5. PubMed ID: 8840235 [TBL] [Abstract][Full Text] [Related]
4. Acute neonatal and benign citrullinaemia in one sibship. Burgess EA; Oberholzer VG; Semmens JM; Stern J Arch Dis Child; 1978 Feb; 53(2):179-82. PubMed ID: 646426 [TBL] [Abstract][Full Text] [Related]
5. Definitive cure of hyperammonemia by liver transplantation in urea cycle defects: report of three cases. Jan D; Poggi F; Jouvet P; Rabier D; Laurent J; Beringer A; Hubert P; Saudubray JM; Revillon Y Transplant Proc; 1994 Feb; 26(1):188. PubMed ID: 8108934 [No Abstract] [Full Text] [Related]
6. Complete neurological recovery of an adult patient with type II citrullinemia after living related partial liver transplantation. Yazaki M; Ikeda S; Takei Y; Yanagisawa N; Matsunami H; Hashikura Y; Kawasaki S; Makuuchi M; Kobayashi K; Saheki T Transplantation; 1996 Dec; 62(11):1679-84. PubMed ID: 8970629 [TBL] [Abstract][Full Text] [Related]
7. Kinetic analysis of argininosuccinate synthetase in a variant form of citrullinaemia. Akaboshi I; Endo F; Matsuda I; Saheki T J Inherit Metab Dis; 1983; 6(1):36-9. PubMed ID: 6408307 [TBL] [Abstract][Full Text] [Related]
11. Exclusion of citrullinaemia in the first trimester of pregnancy by direct assay of argininosuccinate synthetase in chorionic villi. Christensen E; Brandt NJ; Philip J; Bang J Prenat Diagn; 1985; 5(4):299-301. PubMed ID: 4048069 [TBL] [Abstract][Full Text] [Related]
12. Citrullinaemia as a cause of neurological disease in neonatal Friesian calves. Harper PA; Healy PJ; Dennis JA; O'Brien JJ; Rayward DH Aust Vet J; 1986 Nov; 63(11):378-9. PubMed ID: 3827779 [No Abstract] [Full Text] [Related]
13. 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]
14. Chronic vomiting in a case of citrullinaemia detected after treatment by total parenteral nutrition. Benque A; Bommelaer G; Rozental G; Cales P; Cathelineau L; Pham Dinh D; Ribet A Gut; 1984 May; 25(5):531-3. PubMed ID: 6425121 [TBL] [Abstract][Full Text] [Related]
15. The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein. Kobayashi K; Sinasac DS; Iijima M; Boright AP; Begum L; Lee JR; Yasuda T; Ikeda S; Hirano R; Terazono H; Crackower MA; Kondo I; Tsui LC; Scherer SW; Saheki T Nat Genet; 1999 Jun; 22(2):159-63. PubMed ID: 10369257 [TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis of bovine citrullinaemia. Healy P; Dennis J; Rawlinson R; Andersson L Res Vet Sci; 1993 Nov; 55(3):271-4. PubMed ID: 8284487 [TBL] [Abstract][Full Text] [Related]
17. Citrullinaemia: the possibility of prenatal diagnosis. Christensen E; Brandt NJ; Philip J; Kennaway NG J Inherit Metab Dis; 1980; 3(3):73-5. PubMed ID: 6775139 [TBL] [Abstract][Full Text] [Related]
18. Increased intracranial pressure in a neonate with citrullinaemia. Wayenberg JL; Vermeylen D; Gerlo E; Pardou A Eur J Pediatr; 1992 Feb; 151(2):132-3. PubMed ID: 1537355 [No Abstract] [Full Text] [Related]
19. Abnormal mRNA for argininosuccinate synthetase in citrullinaemia. Su TS; Beaudet AL; O'Brien WE Nature; 1983 Feb; 301(5900):533-4. PubMed ID: 6823333 [TBL] [Abstract][Full Text] [Related]
20. Liver transplantation for the treatment of urea cycle disorders. Whitington PF; Alonso EM; Boyle JT; Molleston JP; Rosenthal P; Emond JC; Millis JM J Inherit Metab Dis; 1998; 21 Suppl 1():112-8. PubMed ID: 9686349 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]