170 related articles for article (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
[TBL] [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
[TBL] [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
[TBL] [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; 12():41. PubMed ID: 25232290
[TBL] [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
[TBL] [Abstract][Full Text] [Related]
6. 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; 176(8):1035-1045. PubMed ID: 28593405
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. 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; 12(1):49-54. PubMed ID: 26547206
[TBL] [Abstract][Full Text] [Related]
11. 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; 24(7):705-11. PubMed ID: 25413357
[TBL] [Abstract][Full Text] [Related]
12. 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; 13(3):184-9. PubMed ID: 24659122
[TBL] [Abstract][Full Text] [Related]
13. 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; 15(3):237-43. PubMed ID: 27424139
[TBL] [Abstract][Full Text] [Related]
14. 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; 33(10):2539-42. PubMed ID: 23624553
[TBL] [Abstract][Full Text] [Related]
15. 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; 31(3 Suppl 77):60-3. PubMed ID: 24064016
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. 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; 21(6):373-381. PubMed ID: 28409662
[TBL] [Abstract][Full Text] [Related]
20. Lack of association between NPHS2 gene polymorphisms and Henoch-Schönlein purpura nephritis.
Zhang Y; Xudong X; Du L; Gu W; Dai Y; Liu A; Xia Y; Mao J
Arch Dermatol Res; 2007 Jun; 299(3):151-5. PubMed ID: 17393177
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
