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1316 related items for PubMed ID: 19934083

  • 1. MEFV gene compound heterozygous mutations in familial Mediterranean fever phenotype: a retrospective clinical and molecular study.
    Caglayan AO, Demiryilmaz F, Ozyazgan I, Gumus H.
    Nephrol Dial Transplant; 2010 Aug; 25(8):2520-3. PubMed ID: 19934083
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  • 2. [Familial Mediterranean Fever (FMF): from diagnosis to treatment].
    Medlej-Hashim M, Loiselet J, Lefranc G, Mégarbané A.
    Sante; 2004 Aug; 14(4):261-6. PubMed ID: 15745878
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  • 3. Familial Mediterranean fever with a single MEFV mutation: comparison of rare and common mutations in a Turkish paediatric cohort.
    Soylemezoglu O, Kandur Y, Duzova A, Ozkaya O, Kasapcopur O, Baskin E, Fidan K, Yalcinkaya F.
    Clin Exp Rheumatol; 2015 Aug; 33(6 Suppl 94):S152-5. PubMed ID: 26005881
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  • 4. Familial Mediterranean fever in childhood: a single-center experience.
    Barut K, Sahin S, Adrovic A, Sinoplu AB, Yucel G, Pamuk G, Aydın AK, Dasdemir S, Turanlı ET, Buyru N, Kasapcopur O.
    Rheumatol Int; 2018 Jan; 38(1):67-74. PubMed ID: 28828621
    [Abstract] [Full Text] [Related]

  • 5. Familial Mediterranean fever gene mutations in the inner northern region of Turkey and genotype-phenotype correlation in children.
    Yilmaz R, Ozer S, Ozyurt H, Erkorkmaz U, Sahin S.
    J Paediatr Child Health; 2009 Nov; 45(11):641-5. PubMed ID: 19845843
    [Abstract] [Full Text] [Related]

  • 6. The expanded clinical profile and the efficacy of colchicine therapy in Egyptian children suffering from familial Mediterranean fever: a descriptive study.
    Talaat HS, Mohamed MF, El Rifai NM, Gomaa MA.
    Ital J Pediatr; 2012 Dec 04; 38():66. PubMed ID: 23206577
    [Abstract] [Full Text] [Related]

  • 7. MEFV mutations in patients with Familial Mediterranean Fever from the Aegean region of Turkey.
    Akin H, Onay H, Turker E, Cogulu O, Ozkinay F.
    Mol Biol Rep; 2010 Jan 04; 37(1):93-8. PubMed ID: 19449169
    [Abstract] [Full Text] [Related]

  • 8. 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 04; 58(1):31-4. PubMed ID: 25449140
    [Abstract] [Full Text] [Related]

  • 9. MEFV mutations and their relation to major clinical symptoms of Familial Mediterranean Fever.
    Cekin N, Akyurek ME, Pinarbasi E, Ozen F.
    Gene; 2017 Aug 30; 626():9-13. PubMed ID: 28483595
    [Abstract] [Full Text] [Related]

  • 10. Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in Central Anatolia.
    Yildirim ME, Kurtulgan HK, Ozdemir O, Kilicgun H, Aydemir DS, Baser B, Sezgin I.
    Ann Saudi Med; 2019 Aug 30; 39(6):382-387. PubMed ID: 31804137
    [Abstract] [Full Text] [Related]

  • 11. Genotype-phenotype correlation in patients with familial Mediterranean fever in East Anatolia (Turkey).
    Albayrak F, Selcuk NY, Odabas AR, Cetinkaya R, Pirim I.
    Genet Test Mol Biomarkers; 2010 Jun 30; 14(3):325-8. PubMed ID: 20373849
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  • 16. MEFV mutation analysis of familial Mediterranean fever in Japan.
    Tomiyama N, Higashiuesato Y, Oda T, Baba E, Harada M, Azuma M, Yamashita T, Uehara K, Miyazato A, Hatta K, Ohya Y, Iseki K, Jinno Y, Takishita S.
    Clin Exp Rheumatol; 2008 Jun 30; 26(1):13-7. PubMed ID: 18328141
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  • 17. [Familial Mediterranean fever as representative autoinflammatory disease].
    Yamazaki K, Yamazaki T, Masumoto J, Suzuki A, Yazaki M, Agematsu K.
    Rinsho Byori; 2009 Apr 30; 57(4):371-81. PubMed ID: 19489440
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  • 18. Familial Mediterranean fever without MEFV mutations: a case-control study.
    Ben-Zvi I, Herskovizh C, Kukuy O, Kassel Y, Grossman C, Livneh A.
    Orphanet J Rare Dis; 2015 Mar 25; 10():34. PubMed ID: 25887307
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  • 19. A case of familial Mediterranean fever associated with compound heterozygosity for the pyrin variant L110P-E148Q/M680I in Japan.
    Oshima K, Yamazaki K, Nakajima Y, Kobayashi A, Kato T, Ohara O, Agematsu K.
    Mod Rheumatol; 2010 Apr 25; 20(2):193-5. PubMed ID: 19967574
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