289 related articles for article (PubMed ID: 18414167)
1. 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]
2. Hyperammonemia in a patient with late-onset ornithine carbamoyltransferase deficiency.
Choi DE; Lee KW; Shin YT; Na KR
J Korean Med Sci; 2012 May; 27(5):556-9. PubMed ID: 22563224
[TBL] [Abstract][Full Text] [Related]
3. A Proposed Physiopathological Pathway to Hyperammonemic Encephalopathy in a Non-Cirrhotic Patient with Fibrolamellar Hepatocellular Carcinoma without Ornithine Transcarbamylase (OTC) Mutation.
Surjan RC; Dos Santos ES; Basseres T; Makdissi FF; Machado MA
Am J Case Rep; 2017 Mar; 18():234-241. PubMed ID: 28270654
[TBL] [Abstract][Full Text] [Related]
4. Adult-onset ornithine transcarbamylase (OTC) deficiency unmasked by the Atkins' diet.
Ben-Ari Z; Dalal A; Morry A; Pitlik S; Zinger P; Cohen J; Fattal I; Galili-Mosberg R; Tessler D; Baruch RG; Nuoffer JM; Largiader CR; Mandel H
J Hepatol; 2010 Feb; 52(2):292-5. PubMed ID: 20031247
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Ornithine transcarbamoylase deficiency presenting with acute liver failure.
Mustafa A; Clarke JT
J Inherit Metab Dis; 2006 Aug; 29(4):586. PubMed ID: 16802108
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. 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]
12. [A case of ornithine transcarbamylase deficiency presenting severe symptoms in adulthood].
Shiro Y; Yabuki S
Rinsho Shinkeigaku; 1992 Jul; 32(7):752-4. PubMed ID: 1291170
[TBL] [Abstract][Full Text] [Related]
13. Hyperammonemic Encephalopathy Associated With Fibrolamellar Hepatocellular Carcinoma: Case Report, Literature Review, and Proposed Treatment Algorithm.
Chapuy CI; Sahai I; Sharma R; Zhu AX; Kozyreva ON
Oncologist; 2016 Apr; 21(4):514-20. PubMed ID: 26975868
[TBL] [Abstract][Full Text] [Related]
14. Genotype-Phenotype Correlations in Ornithine Transcarbamylase Deficiency: A Mutation Update.
Caldovic L; Abdikarim I; Narain S; Tuchman M; Morizono H
J Genet Genomics; 2015 May; 42(5):181-94. PubMed ID: 26059767
[TBL] [Abstract][Full Text] [Related]
15. [Ornithine transcarbamylase deficiency in adult].
Brajon D; Carassou P; Pruna L; Feillet F; Kaminsky P
Rev Med Interne; 2010 Oct; 31(10):709-11. PubMed ID: 20570026
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Hyperammonemic coma in a patient with late-onset OTC deficiency.
D'Onofrio V; Poma F; Enea A; Santarelli F; Lovera C; Spada M
Pediatr Med Chir; 2014 Jun; 36(3):9. PubMed ID: 25573644
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [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]
20. Ornithine transcarbamylase deficiency diagnosed in pregnancy.
Celik O; Buyuktas D; Aydin A; Acbay O
Gynecol Endocrinol; 2011 Dec; 27(12):1052-4. PubMed ID: 21736537
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]