334 related articles for article (PubMed ID: 34035022)
21. 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]
22. 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]
23. Posterior fossa syndrome in a patient with an ornithine transcarbamylase deficiency.
Nedermeijer SC; van den Hout J; Geleijns C; de Klerk H; Catsman-Berrevoets CE
Eur J Paediatr Neurol; 2015 May; 19(3):364-6. PubMed ID: 25687292
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Ornithine transcarbamylase deficiency in pregnancy.
Cordero DR; Baker J; Dorinzi D; Toffle R
J Inherit Metab Dis; 2005; 28(2):237-40. PubMed ID: 15877212
[TBL] [Abstract][Full Text] [Related]
26. Acute Presentation and Management of the Encephalopathic Child With an Undiagnosed Inborn Error of Metabolism.
Bennett EE; Hummel K; Smith AG; Longo N
J Emerg Med; 2019 Jan; 56(1):e5-e8. PubMed ID: 30420308
[TBL] [Abstract][Full Text] [Related]
27. Neuromyelitis Optica Complicated by Ornithine Transcarbamylase Deficiency Treated Safely with Pulse Steroid Therapy.
Yoshida R; Sasaki T; Sunouchi T; Ueda M; Kitamura M; Nakayama T; Saito J; Imafuku I
Intern Med; 2021 Oct; 60(20):3321-3324. PubMed ID: 33867389
[TBL] [Abstract][Full Text] [Related]
28. Fatal ammonia toxicity in an adult due to an undiagnosed urea cycle defect: under-recognition of ornithine transcarbamylase deficiency.
Thurlow VR; Asafu-Adjaye M; Agalou S; Rahman Y
Ann Clin Biochem; 2010 May; 47(Pt 3):279-81. PubMed ID: 20406775
[TBL] [Abstract][Full Text] [Related]
29. Corticosteroid suppresses urea-cycle-related gene expressions in ornithine transcarbamylase deficiency.
Imoto K; Tanaka M; Goya T; Aoyagi T; Takahashi M; Kurokawa M; Tashiro S; Kato M; Kohjima M; Ogawa Y
BMC Gastroenterol; 2022 Mar; 22(1):144. PubMed ID: 35346058
[TBL] [Abstract][Full Text] [Related]
30. OTC gene in ornithine transcarbamylase deficiency: clinical course and mutational spectrum in seven Korean patients.
Lee JH; Kim GH; Yoo HW; Cheon CK
Pediatr Neurol; 2014 Sep; 51(3):354-359.e1. PubMed ID: 25011434
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. 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]
33. Late diagnosis of ornithine transcarbamylase defect in three related female patients: polymorphic presentations.
Legras A; Labarthe F; Maillot F; Garrigue MA; Kouatchet A; Ogier de Baulny H
Crit Care Med; 2002 Jan; 30(1):241-4. PubMed ID: 11902270
[TBL] [Abstract][Full Text] [Related]
34. The molecular basis of ornithine transcarbamylase deficiency.
Tuchman M; McCullough BA; Yudkoff M
Eur J Pediatr; 2000 Dec; 159 Suppl 3():S196-8. PubMed ID: 11216899
[TBL] [Abstract][Full Text] [Related]
35. [Fulminant coma: think hyperammonemia and urea cycle disorders].
Augris C; Jouvet P; Benabdelmalek F; Vauquelin P; Caramella JP
Ann Fr Anesth Reanim; 2002 Dec; 21(10):820-3. PubMed ID: 12534125
[TBL] [Abstract][Full Text] [Related]
36. Acute postpartum mental status change and coma caused by previously undiagnosed ornithine transcarbamylase deficiency.
Peterson DE
Obstet Gynecol; 2003 Nov; 102(5 Pt 2):1212-5. PubMed ID: 14607061
[TBL] [Abstract][Full Text] [Related]
37. Continuous arteriovenous hemodiafiltration in the acute treatment of hyperammonaemia due to ornithine transcarbamylase deficiency.
Chen CY; Chen YC; Fang JT; Huang CC
Ren Fail; 2000 Nov; 22(6):823-36. PubMed ID: 11104170
[TBL] [Abstract][Full Text] [Related]
38. Hyperammonemia in ornithine transcarbamylase-deficient recipients following living donor liver transplantation from heterozygous carrier donors.
Rahayatri TH; Uchida H; Sasaki K; Shigeta T; Hirata Y; Kanazawa H; Mali V; Fukuda A; Sakamoto S; Kasahara M
Pediatr Transplant; 2017 Feb; 21(1):. PubMed ID: 27891735
[TBL] [Abstract][Full Text] [Related]
39. Hyperammonaemic Encephalopathy Caused by Adult-Onset Ornithine Transcarbamylase Deficiency.
Niclasen BH; Schelde-Olesen MT; Astvad M; Løkke A; Krøigård T; Nielsen HH
Brain Sci; 2022 Feb; 12(2):. PubMed ID: 35203994
[TBL] [Abstract][Full Text] [Related]
40. [Consensus on diagnosis and treatment of ornithine trans-carbamylase deficiency].
Division of Genetics and Metabolism, Child Diseases and Health Care Branch, Chinese Association for Maternal and Child Health
Zhejiang Da Xue Xue Bao Yi Xue Ban; 2020 Oct; 49(5):539-547. PubMed ID: 33210478
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]