BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

229 related articles for article (PubMed ID: 24485820)

  • 1. Significant hepatic involvement in patients with ornithine transcarbamylase deficiency.
    Gallagher RC; Lam C; Wong D; Cederbaum S; Sokol RJ
    J Pediatr; 2014 Apr; 164(4):720-725.e6. PubMed ID: 24485820
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Frequency and Pathophysiology of Acute Liver Failure in Ornithine Transcarbamylase Deficiency (OTCD).
    Laemmle A; Gallagher RC; Keogh A; Stricker T; Gautschi M; Nuoffer JM; Baumgartner MR; Häberle J
    PLoS One; 2016; 11(4):e0153358. PubMed ID: 27070778
    [TBL] [Abstract][Full Text] [Related]  

  • 3. High urgency liver transplantation in ornithine transcarbamylase deficiency presenting with acute liver failure.
    Teufel U; Weitz J; Flechtenmacher C; Prietsch V; Schmidt J; Hoffmann GF; Kölker S; Engelmann G
    Pediatr Transplant; 2011 Sep; 15(6):E110-5. PubMed ID: 21884343
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ornithine Transcarbamylase Deficiency Presenting as Acute Liver Failure in Girls: A Paediatric Case Series.
    Selvanathan A; Hertzog A; Lemberg DA; Ellaway C
    J Pediatr Gastroenterol Nutr; 2020 Aug; 71(2):208-210. PubMed ID: 32265410
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Acute liver dysfunction with delayed peak of serum aminotransferase levels as a presentation of ornithine transcarbamylase deficiency in females.
    Clarkston K; Lee J; Donoghue S; Peters H; Eiroa H; Shah AA; Loomes K; Wen J; Oliver M; Hardikar W; Prada CE; Asai A
    Am J Med Genet A; 2021 Mar; 185(3):909-915. PubMed ID: 33369132
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Liver Failure as the Presentation of Ornithine Transcarbamylase Deficiency in a 13-Month-Old Female.
    Rajabi F; Rodan LH; Jonas MM; Soul JS; Ullrich NJ; Wessel A; Waisbren SE; Tan WH; Berry GT
    JIMD Rep; 2018; 40():17-22. PubMed ID: 28887792
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal treatment of ornithine transcarbamylase deficiency.
    Wilnai Y; Blumenfeld YJ; Cusmano K; Hintz SR; Alcorn D; Benitz WE; Berquist WE; Bernstein JA; Castillo RO; Concepcion W; Cowan TM; Cox KL; Lyell DJ; Esquivel CO; Homeyer M; Hudgins L; Hurwitz M; Palma JP; Schelley S; Akula VP; Summar ML; Enns GM
    Mol Genet Metab; 2018 Mar; 123(3):297-300. PubMed ID: 29396029
    [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. Retrospective evaluations revealed pre-symptomatic citrulline concentrations measured by newborn screening were significantly low in late-onset ornithine transcarbamylase deficiency patients.
    Lee T; Yoshii K; Yoshida S; Suga T; Nakamura K; Sasai H; Murayama K; Kobayashi H; Hasegawa Y; Takeshima Y
    Clin Chim Acta; 2020 Nov; 510():633-637. PubMed ID: 32828733
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Establishment of ornithine transcarbamylase deficiency-derived primary human hepatocyte with hepatic functions.
    Su S; Di Poto C; Kroemer AH; Cui W; Roy R; Liu X; Ressom HW
    Exp Cell Res; 2019 Nov; 384(1):111621. PubMed ID: 31513782
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Liver transplantation in rare late-onset ornithine transcarbamylase deficiency with central nervous system injury: A case report and review of the literature.
    Jin X; Zeng X; Zhao D; Jiang N
    Brain Behav; 2022 Oct; 12(10):e2765. PubMed ID: 36128655
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Anesthetic implications of ornithine transcarbamylase deficiency.
    Dutoit AP; Flick RR; Sprung J; Babovic-Vuksanovic D; Weingarten TN
    Paediatr Anaesth; 2010 Jul; 20(7):666-73. PubMed ID: 20497355
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An integrated approach to the diagnosis and prospective management of partial ornithine transcarbamylase deficiency.
    Scaglia F; Zheng Q; O'Brien WE; Henry J; Rosenberger J; Reeds P; Lee B
    Pediatrics; 2002 Jan; 109(1):150-2. PubMed ID: 11773558
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Late-Onset Ornithine Transcarbamylase Deficiency Complicated with Extremely High Serum Ammonia Level: Prompt Induction of Hemodialysis as the Key to Successful Treatment.
    Yamamoto S; Yamashita S; Kakiuchi T; Kurogi K; Nishi TM; Tago M; Yamashita SI
    Am J Case Rep; 2022 Nov; 23():e937658. PubMed ID: 36377209
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Activity of the liver enzyme ornithine carbamoyltransferase (OTC) in blood: LC-MS/MS assay for non-invasive diagnosis of ornithine carbamoyltransferase deficiency.
    Krijt J; Sokolová J; Ješina P; Dvořáková L; Řeboun M; Brennerová K; Mistrík M; Zeman J; Honzík T; Kožich V
    Clin Chem Lab Med; 2017 Jul; 55(8):1168-1177. PubMed ID: 28107167
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Maternal ornithine transcarbamylase deficiency, a genetic condition associated with high maternal and neonatal mortality every clinician should know: A systematic review.
    Torkzaban M; Haddad A; Baxter JK; Berghella V; Gahl WA; Al-Kouatly HB
    Am J Med Genet A; 2019 Oct; 179(10):2091-2100. PubMed ID: 31441224
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Are asymptomatic carriers of OTC deficiency always asymptomatic? A multicentric retrospective study of risk using the UCDC longitudinal study database.
    Sen K; Izem R; Long Y; Jiang J; Konczal LL; McCarter RJ; ; Gropman AL; Bedoyan JK
    Mol Genet Genomic Med; 2024 Apr; 12(4):e2443. PubMed ID: 38634223
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Ornithine transcarbamylase deficiency unmasked because of gastrointestinal bleeding.
    Trivedi M; Zafar S; Spalding MJ; Jonnalagadda S
    J Clin Gastroenterol; 2001 Apr; 32(4):340-3. PubMed ID: 11276280
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.