178 related articles for article (PubMed ID: 12637287)
1. Brain MR imaging in acute hyperammonemic encephalopathy arising from late-onset ornithine transcarbamylase deficiency.
Takanashi J; Barkovich AJ; Cheng SF; Kostiner D; Baker JC; Packman S
AJNR Am J Neuroradiol; 2003 Mar; 24(3):390-3. PubMed ID: 12637287
[TBL] [Abstract][Full Text] [Related]
2. Brain MR imaging in neonatal hyperammonemic encephalopathy resulting from proximal urea cycle disorders.
Takanashi J; Barkovich AJ; Cheng SF; Weisiger K; Zlatunich CO; Mudge C; Rosenthal P; Tuchman M; Packman S
AJNR Am J Neuroradiol; 2003; 24(6):1184-7. PubMed ID: 12812952
[TBL] [Abstract][Full Text] [Related]
3. MRI in a woman with late onset ornithine transcarbamylase deficiency.
Manto A; De Gennaro A; Serino A; Cozzolino A; Colasante AG; La Rocca MR
Neuroradiol J; 2010 Sep; 23(4):398-401. PubMed ID: 24148626
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. [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]
7. Ornithine transcarbamylase deficiency in females: an often overlooked cause of treatable encephalopathy.
Pridmore CL; Clarke JT; Blaser S
J Child Neurol; 1995 Sep; 10(5):369-74. PubMed ID: 7499756
[TBL] [Abstract][Full Text] [Related]
8. A novel mutation in ornithine transcarbamylase gene causing mild intermittent hyperammonemia.
Mohamed S; Hamad MH; Kondkar AA; Abu-Amero KK
Saudi Med J; 2015 Oct; 36(10):1229-32. PubMed ID: 26446336
[TBL] [Abstract][Full Text] [Related]
9. Ornithine transcarbamylase deficiency presenting as hepatitis.
Aronson PL; Mistry RD
Pediatr Emerg Care; 2011 Jun; 27(6):527-9. PubMed ID: 21642786
[TBL] [Abstract][Full Text] [Related]
10. Parieto-occipital encephalomalacia in neonatal hyperammonemia with ornithine transcarbamylase deficiency: A case report.
Okanishi T; Ito T; Nakajima Y; Ito K; Kakita H; Yamada Y; Kobayashi S; Ando N; Togari H
Brain Dev; 2010 Aug; 32(7):567-70. PubMed ID: 19640662
[TBL] [Abstract][Full Text] [Related]
11. Acute hyperammonemic encephalopathy in adult onset ornithine transcarbamylase deficiency.
Panlaqui OM; Tran K; Johns A; McGill J; White H
Intensive Care Med; 2008 Oct; 34(10):1922-4. PubMed ID: 18651132
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Ornithine transcarbamylase (OTC) deficiency based on a hemizygous p.R277W mutation causing life-threatening hyperammonemic crisis during treatment for Hodgkin's lymphoma.
Ritter E; Husain RA; Hinderhofer K; Prell T; Fricke HJ; Scholl S; Hochhaus A; La Rosée P
Ann Hematol; 2011 Jul; 90(7):857-9. PubMed ID: 21061009
[No Abstract] [Full Text] [Related]
14. 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]
15. 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]
16. Improved quality of life and unchanged magnetic resonance brain imaging after living donor liver transplantation for late-onset ornithine transcarbamylase deficiency: report of a case.
Kawagishi N; Satoh K; Enomoto Y; Akamatsu Y; Sekiguchi S; Satoh A; Fujimori K; Takasago Y; Ito T; Ohura T; Satomi S
Surg Today; 2005; 35(12):1087-91. PubMed ID: 16341494
[TBL] [Abstract][Full Text] [Related]
17. Ornithine transcarbamylase deficiency presenting with acute reversible cortical blindness.
Prasun P; Altinok D; Misra VK
J Child Neurol; 2015 May; 30(6):782-5. PubMed ID: 24850570
[TBL] [Abstract][Full Text] [Related]
18. Postchemotherapy hyperammonemic encephalopathy emulating ornithine transcarbamoylase (OTC) deficiency.
Chan JS; Harding CO; Blanke CD
South Med J; 2008 May; 101(5):543-5. PubMed ID: 18414167
[TBL] [Abstract][Full Text] [Related]
19. MRI findings in acute hyperammonemic encephalopathy resulting from decompensated chronic liver disease.
Sureka J; Jakkani RK; Panwar S
Acta Neurol Belg; 2012 Jun; 112(2):221-3. PubMed ID: 22426669
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
