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Journal Abstract Search

164 related items for PubMed ID: 12415598

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  • 3. Characteristics of vascular involvement in Behçet's disease.
    Düzgün N, Ateş A, Aydintuğ OT, Demir O, Olmez U.
    Scand J Rheumatol; 2006; 35(1):65-8. PubMed ID: 16467046
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  • 7. Vascular involvement in Behçet's disease: a retrospective analysis of 2319 cases.
    Sarica-Kucukoglu R, Akdag-Kose A, KayabalI M, Yazganoglu KD, Disci R, Erzengin D, Azizlerli G.
    Int J Dermatol; 2006 Aug; 45(8):919-21. PubMed ID: 16911374
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  • 10. A histopathological approach: when papulopustular lesions should be in the diagnostic criteria of Behçet's disease?
    Kalkan G, Karadag AS, Astarci HM, Akbay G, Ustun H, Eksioglu M.
    J Eur Acad Dermatol Venereol; 2009 Sep; 23(9):1056-60. PubMed ID: 19453803
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  • 11. Behçet's disease in southern Chinese patients.
    Mok CC, Cheung TC, Ho CT, Lee KW, Lau CS, Wong RW.
    J Rheumatol; 2002 Aug; 29(8):1689-93. PubMed ID: 12180731
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  • 14. Demographic and clinical properties of juvenile-onset Behçet's disease: A controlled multicenter study.
    Karincaoglu Y, Borlu M, Toker SC, Akman A, Onder M, Gunasti S, Usta A, Kandi B, Durusoy C, Seyhan M, Utas S, Saricaoglu H, Ozden MG, Uzun S, Tursen U, Cicek D, Donmez L, Alpsoy E.
    J Am Acad Dermatol; 2008 Apr; 58(4):579-84. PubMed ID: 18045733
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  • 16. Androgen receptor levels in the sebaceous glands of papulopustular lesions from patients with Behçet's disease and acne vulgaris: a controlled study.
    Durusoy C, Alpsoy E, Elpek O, Karpuzoglu G.
    Adv Clin Path; 2002 Apr; 6(2):87-93. PubMed ID: 19753730
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  • 17. The functional role of nuclear factor kappa-kappaB1 -94 ins/del ATTG promotor gene polymorphism in Behçet's disease: an exploratory study.
    Yalcin B, Atakan N, Alli N.
    Clin Exp Dermatol; 2008 Aug; 33(5):629-33. PubMed ID: 18616724
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  • 19. CTLA-4 gene 49A/G polymorphism in Turkish patients with Behçet's disease.
    Sallakci N, Bacanli A, Coskun M, Yavuzer U, Alpsoy E, Yegin O.
    Clin Exp Dermatol; 2005 Sep; 30(5):546-50. PubMed ID: 16045690
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  • 20. Association of the R92Q TNFRSF1A mutation and extracranial deep vein thrombosis in patients with Behçet's disease.
    Amoura Z, Dodé C, Hue S, Caillat-Zucman S, Bahram S, Delpech M, Grateau G, Wechsler B, Piette JC.
    Arthritis Rheum; 2005 Feb; 52(2):608-11. PubMed ID: 15692984
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