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Journal Abstract Search

148 related items for PubMed ID: 24064016

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Increased prevalence of MEFV exon 10 variants in Japanese patients with adult-onset Still's disease.
    Nonaka F, Migita K, Jiuchi Y, Shimizu T, Umeda M, Iwamoto N, Fujikawa K, Izumi Y, Mizokami A, Nakashima M, Ueki Y, Yasunami M, Kawakami A, Eguchi K.
    Clin Exp Immunol; 2015 Mar; 179(3):392-7. PubMed ID: 25286988
    [Abstract] [Full Text] [Related]

  • 3. The association of TNFRSF1A gene and MEFV gene mutations with adult onset Still's disease.
    Cosan F, Emrence Z, Erbag G, Azakli H, Yilmazer B, Yazici A, Ekmekci SS, Abaci N, Ustek D, Cefle A.
    Rheumatol Int; 2013 Jul; 33(7):1675-80. PubMed ID: 23269568
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  • 4. Serum amyloid A1 (SAA1) gene polymorphisms in Japanese patients with adult-onset Still's disease.
    Yashiro M, Furukawa H, Asano T, Sato S, Kobayashi H, Watanabe H, Suzuki E, Nakamura T, Koga T, Shimizu T, Umeda M, Nonaka F, Ueki Y, Eguchi K, Kawakami A, Migita K.
    Medicine (Baltimore); 2018 Dec; 97(49):e13394. PubMed ID: 30544414
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  • 5. Effects of HLA-DRB1 alleles on susceptibility and clinical manifestations in Japanese patients with adult onset Still's disease.
    Asano T, Furukawa H, Sato S, Yashiro M, Kobayashi H, Watanabe H, Suzuki E, Ito T, Ubara Y, Kobayashi D, Iwanaga N, Izumi Y, Fujikawa K, Yamasaki S, Nakamura T, Koga T, Shimizu T, Umeda M, Nonaka F, Yasunami M, Ueki Y, Eguchi K, Tsuchiya N, Tohma S, Yoshiura KI, Ohira H, Kawakami A, Migita K.
    Arthritis Res Ther; 2017 Sep 12; 19(1):199. PubMed ID: 28899403
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  • 6. Evidence for genetic overlap between adult onset Still's disease and hereditary periodic fever syndromes.
    Sighart R, Rech J, Hueber A, Blank N, Löhr S, Reis A, Sticht H, Hüffmeier U.
    Rheumatol Int; 2018 Jan 12; 38(1):111-120. PubMed ID: 29159471
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  • 9. MEFV gene mutations in Henoch-Schönlein purpura.
    Altug U, Ensari C, Sayin DB, Ensari A.
    Int J Rheum Dis; 2013 Jun 12; 16(3):347-51. PubMed ID: 23981758
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  • 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 12; 24(7):705-11. PubMed ID: 25413357
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  • 12. A case of adult onset Still's disease with mutations of the MEFV gene who is partially responsive to colchicine.
    Ou-Yang LJ, Tang KT.
    Medicine (Baltimore); 2018 Apr 12; 97(15):e0333. PubMed ID: 29642170
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  • 14. Molecular genetic analysis for periodic fever syndromes: a supplemental role for the diagnosis of adult-onset Still's disease.
    Li H, Abramova I, Chesoni S, Yao Q.
    Clin Rheumatol; 2018 Aug 12; 37(8):2021-2026. PubMed ID: 29909561
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  • 15. The frequency of MEFV gene mutations in Behcet's disease and their relation with clinical findings.
    Yazici A, Cefle A, Savli H.
    Rheumatol Int; 2012 Oct 12; 32(10):3025-30. PubMed ID: 21901355
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  • 17. Common Mediterranean fever (MEFV) gene mutations associated with ankylosing spondylitis in Turkish population.
    Yigit S, Inanir A, Karakus N, Kesici E, Bozkurt N.
    Dis Markers; 2012 Oct 12; 33(3):113-8. PubMed ID: 22960328
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  • 18. 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 12; 77(1):32-5. PubMed ID: 20031469
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  • 20. The differential contribution of MEFV mutant alleles to the clinical profile of familial Mediterranean fever.
    Gershoni-Baruch R, Brik R, Shinawi M, Livneh A.
    Eur J Hum Genet; 2002 Feb 12; 10(2):145-9. PubMed ID: 11938447
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