137 related articles for article (PubMed ID: 18843775)
1. 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]
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. 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]
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. 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]
6. 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]
7. 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]
8. 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]
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. 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]
11. 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]
12. Common MEFV gene mutations in Turkish patients with Behcet's disease.
Tasliyurt T; Yigit S; Rustemoglu A; Gul U; Ates O
Gene; 2013 Nov; 530(1):100-3. PubMed ID: 23973724
[TBL] [Abstract][Full Text] [Related]
13. Prevalence and significance of MEFV gene mutations in patients with sarcoidosis.
Sever F; Kobak S; Goksel Ö; Goksel T; Orman M; Berdeli A
Scand J Rheumatol; 2016; 45(3):215-8. PubMed ID: 27053370
[TBL] [Abstract][Full Text] [Related]
14. A study of familial Mediterranean Fever (MEFV) gene mutations in Egyptian children with type 1 diabetes mellitus.
Anwar GM; Fouad HM; Abd El-Hamid A; Mahmoud F; Musa N; Lotfi H; Salah N
Eur J Med Genet; 2015 Jan; 58(1):31-4. PubMed ID: 25449140
[TBL] [Abstract][Full Text] [Related]
15. The carrier rate and spectrum of MEFV gene mutations in central and southeastern European populations.
Debeljak M; Toplak N; Abazi N; Szabados B; Mulaosmanović V; Radović J; Perko D; Vojnović J; Constantin T; Kuzmanovska D; Avčin T
Clin Exp Rheumatol; 2015; 33(6 Suppl 94):S19-23. PubMed ID: 26399837
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Prevalence and significance of MEFV gene mutations in a cohort of patients with rheumatoid arthritis.
Koca SS; Etem EO; Isik B; Yuce H; Ozgen M; Dag MS; Isik A
Joint Bone Spine; 2010 Jan; 77(1):32-5. PubMed ID: 20031469
[TBL] [Abstract][Full Text] [Related]
18. MEFV gene 3'-UTR Alu repeat polymorphisms in patients with familial Mediterranean fever.
Ustek D; Ekmekçi C; Oku B; Coşan F; Cakiris A; Abaci N; Celik S; Kamali S; Hatemi G; Kasapçopur O; Ozdoğan H; Gül A
Clin Exp Rheumatol; 2008; 26(4 Suppl 50):S72-6. PubMed ID: 19026119
[TBL] [Abstract][Full Text] [Related]
19. Prevalence of the MEFV gene mutations in childhood polyarteritis nodosa.
Yalçinkaya F; Ozçakar ZB; Kasapçopur O; Oztürk A; Akar N; Bakkaloğlu A; Arisoy N; Ekim M; Ozen S
J Pediatr; 2007 Dec; 151(6):675-8. PubMed ID: 18035151
[TBL] [Abstract][Full Text] [Related]
20. MEFV mutations in systemic onset juvenile idiopathic arthritis.
Ayaz NA; Ozen S; Bilginer Y; Ergüven M; Taşkiran E; Yilmaz E; Beşbaş N; Topaloğlu R; Bakkaloğlu A
Rheumatology (Oxford); 2009 Jan; 48(1):23-5. PubMed ID: 18984609
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]