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Journal Abstract Search

175 related items for PubMed ID: 20602240

  • 1. MEFV E148Q polymorphism is associated with Henoch-Schönlein purpura in Chinese children.
    He X, Lu H, Kang S, Luan J, Liu Z, Yin W, Yao H, Ding Y, Li T, Heng CK.
    Pediatr Nephrol; 2010 Oct; 25(10):2077-82. PubMed ID: 20602240
    [Abstract] [Full Text] [Related]

  • 2. MEFV gene mutations in Henoch-Schönlein purpura.
    Altug U, Ensari C, Sayin DB, Ensari A.
    Int J Rheum Dis; 2013 Jun; 16(3):347-51. PubMed ID: 23981758
    [Abstract] [Full Text] [Related]

  • 3. The association between MEFV gene polymorphisms and Henoch-Schönlein purpura, and additional SNP-SNP interactions in Chinese Han children.
    Xiong S, Xiong Y, Huang Q, Wang J, Zhang X.
    Rheumatol Int; 2017 Mar; 37(3):455-460. PubMed ID: 27796522
    [Abstract] [Full Text] [Related]

  • 4. MEFV gene mutations in Egyptian children with Henoch-Schonlein purpura.
    Salah S, Rizk S, Lotfy HM, El Houchi S, Marzouk H, Farag Y.
    Pediatr Rheumatol Online J; 2014 Mar; 12():41. PubMed ID: 25232290
    [Abstract] [Full Text] [Related]

  • 5. Association between IL17A and IL17F polymorphisms and risk of Henoch-Schonlein purpura in Chinese children.
    Xu H, Pan Y, Li W, Fu H, Zhang J, Shen H, Han X.
    Rheumatol Int; 2016 Jun; 36(6):829-35. PubMed ID: 27021337
    [Abstract] [Full Text] [Related]

  • 6. Associations of MEFV gene variants, IL-33, and sST2 with the risk of Henoch-Schönlein purpura in children.
    Ruan Y, Xie L.
    Heliyon; 2024 Apr 30; 10(8):e29469. PubMed ID: 38655333
    [Abstract] [Full Text] [Related]

  • 7. Inducible nitric oxide synthase gene polymorphisms are associated with a risk of nephritis in Henoch-Schönlein purpura children.
    Jiang J, Duan W, Shang X, Wang H, Gao Y, Tian P, Zhou Q.
    Eur J Pediatr; 2017 Aug 30; 176(8):1035-1045. PubMed ID: 28593405
    [Abstract] [Full Text] [Related]

  • 8. MEFV mutations modify the clinical presentation of Henoch-Schönlein purpura.
    Ozçakar ZB, Yalçinkaya F, Cakar N, Acar B, Kasapçopur O, Ugüten D, Soy D, Kara N, Uncu N, Arisoy N, Ekim M.
    J Rheumatol; 2008 Dec 30; 35(12):2427-9. PubMed ID: 18843775
    [Abstract] [Full Text] [Related]

  • 9. Prevalence and significance of the MEFV gene mutations in childhood Henoch-Schönlein purpura without FMF symptoms.
    Dogan CS, Akman S, Koyun M, Bilgen T, Comak E, Gokceoglu AU.
    Rheumatol Int; 2013 Feb 30; 33(2):377-80. PubMed ID: 22451026
    [Abstract] [Full Text] [Related]

  • 10. MEFV mutations in Iranian Azari Turkish patients with Henoch-Schönlein purpura.
    Bonyadi M, Younesi M, Rafeey M, Sadeghi Shabestari M, Mortazavi F.
    Turk J Med Sci; 2016 Jun 23; 46(4):967-71. PubMed ID: 27513391
    [Abstract] [Full Text] [Related]

  • 11. Heat shock protein 70-2 and tumor necrosis factor-α gene polymorphisms in Chinese children with Henoch-Schönlein purpura.
    Ding GX, Wang CH, Che RC, Guan WZ, Yuan YG, Su M, Zhang AH, Huang SM.
    World J Pediatr; 2016 Feb 23; 12(1):49-54. PubMed ID: 26547206
    [Abstract] [Full Text] [Related]

  • 12. Familial Mediterranean fever gene (MEFV) mutations and disease severity in systemic lupus erythematosus (SLE): implications for the role of the E148Q MEFV allele in inflammation.
    Deniz R, Ozen G, Yilmaz-Oner S, Alibaz-Oner F, Erzik C, Aydin SZ, Inanc N, Eren F, Bayalan F, Direskeneli H, Atagunduz P.
    Lupus; 2015 Jun 23; 24(7):705-11. PubMed ID: 25413357
    [Abstract] [Full Text] [Related]

  • 13. Interferon-gamma gene polymorphism +874 (a/t) in Chinese children with Henoch-Schonlein purpura.
    Xu H, Li W, Fu H, Jiang G.
    Iran J Allergy Asthma Immunol; 2014 Jun 23; 13(3):184-9. PubMed ID: 24659122
    [Abstract] [Full Text] [Related]

  • 14. Lack of Association between Interleukin-8 Gene +781 C/T Polymorphism and Henoch-Schönlein Purpura in Childhood.
    Xu H, Pan YX, Zhang J, Liu Y, Mao JH, Li W.
    Iran J Allergy Asthma Immunol; 2016 Jun 23; 15(3):237-43. PubMed ID: 27424139
    [Abstract] [Full Text] [Related]

  • 15. A study on the association between C1GALT1 polymorphisms and the risk of Henoch-Schönlein purpura in a Chinese population.
    An J, Lü Q, Zhao H, Cao Y, Yan B, Ma Z.
    Rheumatol Int; 2013 Oct 23; 33(10):2539-42. PubMed ID: 23624553
    [Abstract] [Full Text] [Related]

  • 16. MEFV gene mutations and their clinical significance in Korean patients with adult-onset Still's disease.
    Kim JJ, Kim JK, Shim SC, Choe JY, Kim TH, Jun JB, Yoo DH.
    Clin Exp Rheumatol; 2013 Oct 23; 31(3 Suppl 77):60-3. PubMed ID: 24064016
    [Abstract] [Full Text] [Related]

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  • 18. Lack of effect of the MEFV E148Q polymorphism on IL-1β in Henoch-Schönlein purpura.
    He X, Kang S, Liu Z, Yin W, Ding Y.
    Scand J Rheumatol; 2011 May 23; 40(3):238-9. PubMed ID: 21366387
    [No Abstract] [Full Text] [Related]

  • 19. MEFV gene variants in children with Henoch-Schönlein purpura and association with clinical manifestations: a single-center Mediterranean experience.
    Ekinci RMK, Balci S, Bisgin A, Atmis B, Dogruel D, Altintas DU, Yilmaz M.
    Postgrad Med; 2019 Jan 23; 131(1):68-72. PubMed ID: 30513227
    [Abstract] [Full Text] [Related]

  • 20. Association of Endothelial Nitric Oxide Synthase Gene Polymorphism with Susceptibility and Nephritis Development of Henoch-Schönlein Purpura in Chinese Han Children.
    Wang A, Wang A, Xiao Y, Wang J, Xu E.
    Genet Test Mol Biomarkers; 2017 Jun 23; 21(6):373-381. PubMed ID: 28409662
    [Abstract] [Full Text] [Related]

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