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PUBMED FOR HANDHELDS

Journal Abstract Search


161 related items for PubMed ID: 23570878

  • 1. Association of eNOS gene intron 4 a/b VNTR polymorphisms in children with nephrotic syndrome.
    Dursun H, Noyan A, Matyar S, Buyukcelik M, Soran M, Cengiz N, Bayazit AK, Seydaoglu G, Attila G, Anarat A.
    Gene; 2013 Jun 15; 522(2):192-5. PubMed ID: 23570878
    [Abstract] [Full Text] [Related]

  • 2. MDR-1 gene polymorphisms in steroid-responsive versus steroid-resistant nephrotic syndrome in children.
    Jafar T, Prasad N, Agarwal V, Mahdi A, Gupta A, Sharma RK, Negi MP, Agrawal S.
    Nephrol Dial Transplant; 2011 Dec 15; 26(12):3968-74. PubMed ID: 21460357
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  • 3. Endothelial nitric oxide synthase gene intron 4 a/b VNTR polymorphism in children with APSGN.
    Dursun H, Noyan A, Matyar S, Buyukcelik M, Soran M, Cengiz N, Seydaoglu G, Attila G, Bayazit AK, Anarat A.
    Pediatr Nephrol; 2006 Nov 15; 21(11):1661-5. PubMed ID: 16941147
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  • 4. Genetic dilemma: eNOS gene intron 4a/b VNTR polymorphism in sepsis and its clinical features in Turkish children.
    Celik U, Yildizdaş D, Alhan E, Celik T, Attila G, Sertdemir Y, Tepe T.
    Turk J Pediatr; 2008 Nov 15; 50(2):114-9. PubMed ID: 18664073
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  • 6. [Association of genetic polymorphisms in endothelial nitric oxide synthase 3 gene with recurrent early spontaneous abortion].
    Fan W, Li SW, Wang Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Feb 15; 24(1):23-6. PubMed ID: 17285538
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  • 7. Apolipoprotein E polymorphism in childhood nephrotic syndrome.
    Attila G, Noyan A, Karabay Bayazit A, Acartürk E, Anarat A.
    Pediatr Nephrol; 2002 May 15; 17(5):359-62. PubMed ID: 12042894
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  • 10. Association between achalasia and nitric oxide synthase gene polymorphisms.
    Mearin F, García-González MA, Strunk M, Zárate N, Malagelada JR, Lanas A.
    Am J Gastroenterol; 2006 Sep 15; 101(9):1979-84. PubMed ID: 16848803
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  • 11. Tumor necrosis factor alpha gene polymorphisms and haplotypes in Egyptian children with nephrotic syndrome.
    Youssef DM, El-Shal AS, Hussein S, Salah K, Ahmed AERE.
    Cytokine; 2018 Feb 15; 102():76-82. PubMed ID: 28803697
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  • 14. [Analysis on association of glucocorticoid receptor gene polymorphism with steroid-resistance in idiopathic nephrotic syndrome of children].
    Ye JW, Ding J, Huang JP, Chen Y, Yao Y, Xiao HJ, Yang JY, Shen Y, Meng Q.
    Zhonghua Er Ke Za Zhi; 2003 Sep 15; 41(9):661-5. PubMed ID: 14733805
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  • 15. ACE gene polymorphism in Turkish children with nephrotic syndrome.
    Celik US, Noyan A, Bayazit AK, Büyükçelik M, Dursun H, Anarat A, Attila G, Matyar S.
    Ren Fail; 2006 Sep 15; 28(5):401-3. PubMed ID: 16825089
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  • 16. Genetic variations of the NR3C1 gene in children with sporadic nephrotic syndrome.
    Ye J, Yu Z, Ding J, Chen Y, Huang J, Yao Y, Xiao H, Yang J, Shen Y, Meng Q.
    Biochem Biophys Res Commun; 2006 Sep 22; 348(2):507-13. PubMed ID: 16890204
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  • 17. A genetic study of steroid-resistant nephrotic syndrome: relationship between polymorphism -173 G to C in the MIF gene and serum level MIF in children.
    Ramayani OR, Sekarwana N, Trihono PP, Sadewa AH, Lelo A.
    J Dev Orig Health Dis; 2016 Feb 22; 7(1):102-7. PubMed ID: 26541175
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  • 18. Association analysis of endothelial nitric oxide synthase gene polymorphism with primary hypertension in a Singapore population.
    Moe KT, Lim ST, Wong P, Chua T, DeSilva DA, Koh TH, Wong MC, Chin-Dusting J.
    J Hum Hypertens; 2006 Dec 22; 20(12):956-63. PubMed ID: 17024134
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  • 19. Endothelial nitric oxide synthase polymorphisms associated with abnormal nitric oxide production are not over-represented in children with Down syndrome.
    Cua CL, Cooke G, Taylor M, Hayes J, Waldon L, Lipowski P, Kossman B, Nash PL.
    Congenit Heart Dis; 2006 Jul 22; 1(4):169-74. PubMed ID: 18377542
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  • 20. Association of endothelial nitric oxide synthase gene intron 4 polymorphism with end-stage renal disease.
    Bellini MH, Figueira MN, Piccoli MF, Marumo JT, Cendoroglo MS, Neto MC, Dalboni MA, Batista MC, Goes MA, Schor N.
    Nephrology (Carlton); 2007 Jun 22; 12(3):289-93. PubMed ID: 17498125
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