These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

102 related articles for article (PubMed ID: 26743057)

  • 1. Pride and protein.
    Stern W
    J Inherit Metab Dis; 2016 Mar; 39(2):321-4. PubMed ID: 26743057
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Interjections in the performance of Jane Austen's Pride and prejudice.
    O'Connell DC; Kowal S
    J Psycholinguist Res; 2010 Aug; 39(4):285-304. PubMed ID: 20091122
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. Jane Austen's lifelong health problems and final illness: New evidence points to a fatal Hodgkin's disease and excludes the widely accepted Addison's.
    Upfal A
    Med Humanit; 2005 Jun; 31(1):3-11. PubMed ID: 23674643
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. Inference of personality projected onto fictional characters having an author's first name.
    Barry H
    Psychol Rep; 2001 Dec; 89(3):705-6. PubMed ID: 11824740
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. How reliable is the allopurinol load in detecting carriers for ornithine transcarbamylase deficiency?
    Grünewald S; Fairbanks L; Genet S; Cranston T; Hüsing J; Leonard JV; Champion MP
    J Inherit Metab Dis; 2004; 27(2):179-86. PubMed ID: 15159648
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Evidence for mutational cis-acting factors affecting mutagenesis in the ornithine transcarbamylase gene.
    Azevedo L; Climent C; Vilarinho L; Calafell F; Amorim A
    Hum Mutat; 2004 Sep; 24(3):273. PubMed ID: 15300856
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. [Hyperammonaemia type II as one of the congenital urea cycle defects].
    Ciara E
    Med Wieku Rozwoj; 1999; 3(1):83-95. PubMed ID: 10910641
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. A case with combined rare inborn metabolic disorders: congenital adrenal hyperplasia and ornithine transcarbamylase deficiency.
    Kim YM; Lee BH; Choi JH; Kim GH; Lim HH; Yoo HW
    Gene; 2013 Sep; 527(1):394-6. PubMed ID: 23769969
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Mutations and polymorphisms in the human ornithine transcarbamylase (OTC) gene.
    Yamaguchi S; Brailey LL; Morizono H; Bale AE; Tuchman M
    Hum Mutat; 2006 Jul; 27(7):626-32. PubMed ID: 16786505
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Low citrulline may not be diagnostic of ornithine transcarbamylase deficiency: a case report.
    Chiong MA; Carpenter K; Christodoulou J
    J Inherit Metab Dis; 2007 Jun; 30(3):405. PubMed ID: 17407001
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Fatal hyperammonaemia due to late-onset ornithine transcarbamylase deficiency.
    Bijvoet GP; van der Sijs-Bos CJ; Wielders JP; Groot OA
    Neth J Med; 2016 Jan; 74(1):36-9. PubMed ID: 26819360
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Ornithine transcarbamylase deficiency in females: an often overlooked cause of treatable encephalopathy.
    Pridmore CL; Clarke JT; Blaser S
    J Child Neurol; 1995 Sep; 10(5):369-74. PubMed ID: 7499756
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.