BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

108 related articles for article (PubMed ID: 21231959)

  • 1. Prevalence of MEFV gene mutations and their clinical correlations in Turkish children with Henoch-Schönlein purpura.
    Bayram C; Demircin G; Erdoğan O; Bülbül M; Caltik A; Akyüz SG
    Acta Paediatr; 2011 May; 100(5):745-9. PubMed ID: 21231959
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 12():41. PubMed ID: 25232290
    [TBL] [Abstract][Full Text] [Related]  

  • 3. MEFV gene mutations in children with Henoch-Schönlein purpura and their correlations-do mutations matter?
    Cakici EK; Kurt Şükür ED; Özlü SG; Yazılıtaş F; Özdel S; Gür G; Eroğlu FK; Güngör T; Çelikkaya E; Bağlan E; Bülbül M
    Clin Rheumatol; 2019 Jul; 38(7):1947-1952. PubMed ID: 30826945
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 35(12):2427-9. PubMed ID: 18843775
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 33(2):377-80. PubMed ID: 22451026
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prevalence and significance of mutations in the familial Mediterranean fever gene in Henoch-Schönlein purpura.
    Gershoni-Baruch R; Broza Y; Brik R
    J Pediatr; 2003 Nov; 143(5):658-61. PubMed ID: 14615741
    [TBL] [Abstract][Full Text] [Related]  

  • 8. MEFV gene mutations (M694V, V726A, M680I, and A744S) in Iranian children with Henoch-Schönlein purpura.
    Nikibakhsh AA; Houshmand M; Bagheri M; Zadeh HM; Rad IA
    Pneumologia; 2012; 61(2):84-7. PubMed ID: 22783597
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Effect of paraoxonase 1 gene polymorphisms on clinical course of Henoch-Schönlein purpura.
    Yilmaz A; Emre S; Agachan B; Bilge I; Yilmaz H; Ergen A; Isbir T; Sirin A
    J Nephrol; 2009; 22(6):726-32. PubMed ID: 19967651
    [TBL] [Abstract][Full Text] [Related]  

  • 10. MEFV gene mutations and clinical course in pediatric patients with Henoch-Schönlein purpura.
    Can E; Kılınç Yaprak Z; Hamilçıkan Ş; Erol M; Bostan Gayret Y Özgül Yiğit Ö
    Arch Argent Pediatr; 2018 Jun; 116(3):e385-e391. PubMed ID: 29756710
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Atypical Henoch-Schonlein purpura: a forerunner of familial Mediterranean fever.
    Adiv OE; Butbul Y; Nutenko I; Brik R
    Isr Med Assoc J; 2011 Apr; 13(4):209-11. PubMed ID: 21598807
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 46(4):967-71. PubMed ID: 27513391
    [TBL] [Abstract][Full Text] [Related]  

  • 13. HLA-DRB1 alleles and Henoch-Schönlein purpura: susceptibility and severity of disease.
    Soylemezoglu O; Peru H; Gonen S; Cetinyurek A; Buyan N
    J Rheumatol; 2008 Jun; 35(6):1165-8. PubMed ID: 18412308
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 40(3):238-9. PubMed ID: 21366387
    [No Abstract]   [Full Text] [Related]  

  • 15. Familial Mediterranean fever in Syrian children: phenotype-genotype correlation.
    Jarjour RA; Al-Berrawi S
    Rheumatol Int; 2015 Apr; 35(4):629-34. PubMed ID: 25150514
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Lack of association between macrophage migration inhibitory factor gene promoter (-173 G/C) polymorphism and childhood Henoch-Schönlein purpura in Turkish patients.
    Nalbantoglu S; Tabel Y; Mir S; Berdeli A
    Cytokine; 2013 Apr; 62(1):160-4. PubMed ID: 23523092
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 131(1):68-72. PubMed ID: 30513227
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Childhood Henoch Schonlein purpura in Middle East countries.
    Akl K
    Saudi J Kidney Dis Transpl; 2007 Jun; 18(2):151-8. PubMed ID: 17496388
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Renin-angiotensin system gene polymorphisms in children with Henoch-Schönlein purpura in West China.
    Desong Liu ; Fang Lu ; Songhui Zhai ; Liu Wei ; Shi Ma ; Xiuying Chen ; Liqun Dong ; Yannan Guo ; Jin Wu ; Zheng Wang
    J Renin Angiotensin Aldosterone Syst; 2010 Dec; 11(4):248-55. PubMed ID: 20702504
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Polymorphism at codon 469 of the intercellular adhesion molecule-1 locus is associated with protection against severe gastrointestinal complications in Henoch-Schönlein purpura.
    Amoli MM; Mattey DL; Calviño MC; Garcia-Porrua C; Thomson W; Hajeer AH; Ollier WE; Gonzalez-Gay MA
    J Rheumatol; 2001 May; 28(5):1014-8. PubMed ID: 11361181
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.