140 related articles for article (PubMed ID: 11797036)
1. Fatal hyperammonemic coma caused by ornithine transcarbamylase deficiency in a woman.
Perpoint T; Argaud L; Blanc Q; Robert D
Intensive Care Med; 2001 Dec; 27(12):1962. PubMed ID: 11797036
[No Abstract] [Full Text] [Related]
2. Hyperammonemic coma in an ornithine transcarbamylase mutation carrier following antepartum corticosteroids.
Lipskind S; Loanzon S; Simi E; Ouyang DW
J Perinatol; 2011 Oct; 31(10):682-4. PubMed ID: 21956151
[TBL] [Abstract][Full Text] [Related]
3. Coma query cause.
Wood GE; McNicholas J
BMJ Case Rep; 2015 May; 2015():. PubMed ID: 25948840
[TBL] [Abstract][Full Text] [Related]
4. [Hyperammonaemic coma after valproate therapy as adult onset of ornithine transcarbamylase deficiency].
Padilla Mde L; Miguélez M; Riverola A; Bueno J
Med Clin (Barc); 2002 Feb; 118(5):199. PubMed ID: 11852003
[No Abstract] [Full Text] [Related]
5. Fatal coma in a young adult due to late-onset urea cycle deficiency presenting with a prolonged seizure: a case report.
Alameri M; Shakra M; Alsaadi T
J Med Case Rep; 2015 Nov; 9():267. PubMed ID: 26593089
[TBL] [Abstract][Full Text] [Related]
6. Hyperammonemia in a Woman with Late-onset Ornithine Transcarbamylase Deficiency.
Koya Y; Shibata M; Senju M; Honma Y; Hiura M; Ishii M; Matsumoto S; Harada M
Intern Med; 2019 Apr; 58(7):937-942. PubMed ID: 30449781
[TBL] [Abstract][Full Text] [Related]
7. Successful early management of a female patient with a metabolic stroke due to ornithine transcarbamylase deficiency.
Tummolo A; Favia V; Bellantuono R; Bellino V; Ranieri A; Morrone A; De Palo T; Papadia F
Pediatr Emerg Care; 2013 May; 29(5):656-8. PubMed ID: 23640148
[TBL] [Abstract][Full Text] [Related]
8. [Hyperammonemia type II as an example of urea cycle disorder].
Hawrot-Kawecka AM; Kawecki GP; Duława J
Wiad Lek; 2006; 59(7-8):512-5. PubMed ID: 17209350
[TBL] [Abstract][Full Text] [Related]
9. [Progressing unconsciousness in a young male].
Mäkynen H; Kahri J; Siitonen A; Sipilä I
Duodecim; 2000; 116(17):1841-4. PubMed ID: 12001638
[No Abstract] [Full Text] [Related]
10. Curative Treatment of Ornithine Transcarbamylase Deficiency With a Liver Transplant: A Case Report.
Shamsaeefar A; Nikeghbalian S; Dehghani SM; Kazemi K; Motazedian N; Geramizadeh B; Malekhosseini SA
Exp Clin Transplant; 2019 Feb; 17(1):119-120. PubMed ID: 27447480
[TBL] [Abstract][Full Text] [Related]
11. [Acute hyperammonemic encephalopathy in ornithine transcarbamylase deficiency].
Sánchez Sánchez V; Palomino García A; Pereira Cunill JL; Rodríguez Uranga JJ
Neurologia; 2009 Jun; 24(5):345-6. PubMed ID: 20050118
[No Abstract] [Full Text] [Related]
12. Hyperammonemic coma: beyond hepatic encephalopathy.
Rimar D; Bitterman H
South Med J; 2008 May; 101(5):467-8. PubMed ID: 18414162
[No Abstract] [Full Text] [Related]
13. Adult-onset ornithine transcarbamylase deficiency as a rare cause of fatal hyperammonaemia.
Durer S; Durer C; Hoilat GJ
Lancet; 2021 Aug; 398(10302):e11. PubMed ID: 34454677
[No Abstract] [Full Text] [Related]
14. Late-onset ornithine transcarbamylase deficiency: treatment and outcome of hyperammonemic crisis.
Bergmann KR; McCabe J; Smith TR; Guillaume DJ; Sarafoglou K; Gupta S
Pediatrics; 2014 Apr; 133(4):e1072-6. PubMed ID: 24616362
[TBL] [Abstract][Full Text] [Related]
15. Hyperammonemic encephalopathy in a child with ornithine transcarbamylase deficiency due to a novel combined heterozygous mutations.
Gao J; Gao F; Hong F; Yu H; Jiang P
Am J Emerg Med; 2015 Mar; 33(3):474.e1-3. PubMed ID: 25227973
[TBL] [Abstract][Full Text] [Related]
16. Hyperammonemic coma due to parenteral nutrition in a woman with heterozygous ornithine transcarbamylase deficiency.
Felig DM; Brusilow SW; Boyer JL
Gastroenterology; 1995 Jul; 109(1):282-4. PubMed ID: 7797025
[TBL] [Abstract][Full Text] [Related]
17. Intermittent hyperammonemic encephalopathy in a child with ornithine transcarbamylase deficiency.
Gulati S; Menon S; Kabra M; Kalra V
Indian J Pediatr; 2004 Jul; 71(7):645-7. PubMed ID: 15280615
[TBL] [Abstract][Full Text] [Related]
18. Acute hyperammonemic encephalopathy secondary to ornithine transcarbamylase deficiency in a child: findings in diagnostic imaging.
Miranda GM; Marcon NAP; Basso CF; Jorge Júnior LA; Queiroz RM
Arq Neuropsiquiatr; 2019 Nov; 77(11):834-835. PubMed ID: 31826142
[No Abstract] [Full Text] [Related]
19. Late-onset presentation of ornithine transcarbamylase deficiency in a young woman with hyperammonemic coma.
Gaspari R; Arcangeli A; Mensi S; Wismayer DS; Tartaglione T; Antuzzi D; Conti G; Proietti R
Ann Emerg Med; 2003 Jan; 41(1):104-9. PubMed ID: 12514690
[TBL] [Abstract][Full Text] [Related]
20. A rare cause of postpartum coma: isolated hyperammonemia due to urea cycle disorder.
Açıkalın A; Dişel NR; Direk EÇ; Ilgınel MT; Sebe A; Bıçakçı Ş
Am J Emerg Med; 2016 Jul; 34(7):1324.e3-4. PubMed ID: 26776297
[No Abstract] [Full Text] [Related]
[Next] [New Search]
