120 related articles for article (PubMed ID: 35046116)
21. Fatal cerebral edema from late-onset ornithine transcarbamylase deficiency in a juvenile male patient receiving valproic acid.
Thakur V; Rupar CA; Ramsay DA; Singh R; Fraser DD
Pediatr Crit Care Med; 2006 May; 7(3):273-6. PubMed ID: 16575347
[TBL] [Abstract][Full Text] [Related]
22. Late-onset ornithine transcarbamylase deficiency: a rare cause of recurrent abnormal behavior in adults.
Hidaka M; Higashi E; Uwatoko T; Uwatoko K; Urashima M; Takashima H; Watanabe Y; Kitazono T; Sugimori H
Acute Med Surg; 2020; 7(1):e565. PubMed ID: 32995020
[TBL] [Abstract][Full Text] [Related]
23. Under recognition of late onset ornithine transcarbamylase deficiency.
Schultz RE; Salo MK
Arch Dis Child; 2000 May; 82(5):390-1. PubMed ID: 10799432
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. 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]
26. 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]
27. 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]
28. Clinical outcomes and the mutation spectrum of the OTC gene in patients with ornithine transcarbamylase deficiency.
Choi JH; Lee BH; Kim JH; Kim GH; Kim YM; Cho J; Cheon CK; Ko JM; Lee JH; Yoo HW
J Hum Genet; 2015 Sep; 60(9):501-7. PubMed ID: 25994866
[TBL] [Abstract][Full Text] [Related]
29. Hyperammonemic Encephalopathy Mimicking Ornithine Transcarbamylase Deficiency in Fibrolamellar Hepatocellular Carcinoma: Successful Treatment with Continuous Venovenous Hemofiltration and Ammonia Scavengers.
Lee JS; Jin HY; Ko JM; Kim SH; Han N; Park BK; Park M; Park HJ; Lee JA
Cancer Res Treat; 2021 Jan; 53(1):283-288. PubMed ID: 32898940
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. 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]
32. Early intervention for late-onset ornithine transcarbamylase deficiency.
Fujisawa D; Mitsubuchi H; Matsumoto S; Iwai M; Nakamura K; Hoshide R; Harada N; Yoshino M; Endo F
Pediatr Int; 2015; 57(1):e1-3. PubMed ID: 25711267
[TBL] [Abstract][Full Text] [Related]
33. Clinical and mutation analysis of 24 Chinese patients with ornithine transcarbamylase deficiency.
Shao Y; Jiang M; Lin Y; Mei H; Zhang W; Cai Y; Su X; Hu H; Li X; Liu L
Clin Genet; 2017 Sep; 92(3):318-322. PubMed ID: 28266016
[TBL] [Abstract][Full Text] [Related]
34. Malnutrition with hypoaminoacidemia in a 22-year-old pregnant patient masking a likely ornithine transcarbamylase deficiency.
Lefrère B; Ulmann G; Chartier M; Patkaï J; Cynober L; Neveux N
Clin Nutr ESPEN; 2019 Apr; 30():89-93. PubMed ID: 30904234
[TBL] [Abstract][Full Text] [Related]
35. [Neonate-onset ornithine transcarbamylase deficiency].
Gao RW; Ba Y; Zhang R; Cao Y; Yang L; Wu BB; Zhou WH; Zhou JG
Zhongguo Dang Dai Er Ke Za Zhi; 2023 Apr; 25(4):431-435. PubMed ID: 37073851
[TBL] [Abstract][Full Text] [Related]
36. Novel mutation in OTC gene causes neonatal death in twin brothers.
Nagy GR; Largiadèr CR; Nuoffer JM; Nagy B; Lázár L; Papp Z
J Perinatol; 2007 Feb; 27(2):123-4. PubMed ID: 17262046
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. [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]
39. Complete deletion of ornithine transcarbamylase gene confirmed by CGH array of X chromosome.
Arranz JA; Madrigal I; Riudor E; Armengol L; Milà M
J Inherit Metab Dis; 2007 Oct; 30(5):813. PubMed ID: 17570074
[TBL] [Abstract][Full Text] [Related]
40. Ammonia and coma - a case report of late onset hemizygous ornithine carbamyltransferase deficiency in 68-year-old female.
Marquetand J; Freisinger P; Lindig T; Euler S; Gasser M; Overkamp D
BMC Neurol; 2020 Apr; 20(1):118. PubMed ID: 32252669
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
