BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 24449986)

  • 1. Coagulopathy unmasking hepatic failure in a child with ornithine transcarbamylase deficiency.
    Samuel N; Politansky AK; Hoffman R; Itzkovich S; Mandel H
    Isr Med Assoc J; 2013 Dec; 15(12):777-9. PubMed ID: 24449986
    [No Abstract]   [Full Text] [Related]  

  • 2. Ornithine transcarbamylase deficiency presenting as recurrent abdominal pain in childhood.
    Mhanni AA; Prasad C; Rockman-Greenberg C
    Pediatr Emerg Care; 2011 Sep; 27(9):850-3. PubMed ID: 21926883
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Ornithine transcarbamylase deficiency and pancreatitis.
    Anadiotis G; Ierardi-Curto L; Kaplan PB; Berry GT
    J Pediatr; 2001 Jan; 138(1):123-4. PubMed ID: 11148526
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. [Ornithine transcarbamylase deficiency].
    Matsuda I
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():775-8. PubMed ID: 12013997
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 9. RC--a case of ornithine transcarbamylase (OTC) deficiency. The most commonly genetically acquired urea cycle defect.
    Morra DR; Nadkarni VM; Bartoshesky LE; Finkelstein MS
    Del Med J; 2000 Aug; 72(8):349-54. PubMed ID: 10984978
    [No Abstract]   [Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. A novel mutation of the ornithine transcarbamylase gene leading to fatal hyperammonemia in a liver transplant recipient.
    Mukhtar A; Dabbous H; El Sayed R; Aboulfetouh F; Bahaa M; Abdelaal A; Fathy M; El-Meteini M
    Am J Transplant; 2013 Apr; 13(4):1084-1087. PubMed ID: 23551631
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Ornithine transcarbamylase deficiency of a male newborn with fatal outcome.
    Hartung B; Temme O; Neuen-Jacob E; Ritz-Timme S; Hinderhofer K; Daldrup T
    Int J Legal Med; 2016 May; 130(3):783-5. PubMed ID: 26753873
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Molecular diagnosis of OTC gene mutation in a Chinese family with ornithine transcarbamylase deficiency].
    Meng LL; Jiang T; Qin L; Ma DY; Chen YL; Han SP; Yu ZB; Guo XR; Hu P; Xu ZF
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Apr; 30(2):195-8. PubMed ID: 23568734
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Interaction between murine spf-ash mutation and genetic background yields different metabolic phenotypes.
    Marini JC; Erez A; Castillo L; Lee B
    Am J Physiol Endocrinol Metab; 2007 Dec; 293(6):E1764-71. PubMed ID: 17925451
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Living donor liver transplantation for ornithine transcarbamylase deficiency.
    Wakiya T; Sanada Y; Mizuta K; Umehara M; Urahasi T; Egami S; Hishikawa S; Fujiwara T; Sakuma Y; Hyodo M; Murayama K; Hakamada K; Yasuda Y; Kawarasaki H
    Pediatr Transplant; 2011 Jun; 15(4):390-5. PubMed ID: 21585627
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [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]  

  • 19. Hepatocellular carcinoma in a research subject with ornithine transcarbamylase deficiency.
    Wilson JM; Shchelochkov OA; Gallagher RC; Batshaw ML
    Mol Genet Metab; 2012 Feb; 105(2):263-5. PubMed ID: 22129577
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Presentation of an acquired urea cycle disorder post liver transplantation.
    Ghabril M; Nguyen J; Kramer D; Genco T; Mai M; Rosser BG
    Liver Transpl; 2007 Dec; 13(12):1714-6. PubMed ID: 18044746
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.