Search Results - "Boyvat, A."

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    Lesional activation of Tc17 cells in Behçet disease and psoriasis supports HLA class I‐mediated autoimmune responses by Vural, S., Kerl, K., Ertop Doğan, P., Vollmer, S., Puchta, U., He, M., Arakawa, Y., Heper, A.O., Karal‐Öktem, A., Hartmann, D., Boyvat, A., Prinz, J.C., Arakawa, A.

    Published in British journal of dermatology (1951) (01-12-2021)
    “…Summary Background Behçet disease (BD) presents with lymphocytic and neutrophilic vasculitis of unknown aetiology. HLA‐B*51, the endoplasmic reticulum…”
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    Association of pyrin mutations and autoinflammation with complex phenotype hidradenitis suppurativa: a case–control study by Vural, S., Gündoğdu, M., Gökpınar İli, E., Durmaz, C.D., Vural, A., Steinmüller‐Magin, L., Kleinhempel, A., Holdt, L.M., Ruzicka, T., Giehl, K.A., Ruhi, H.I., Boyvat, A.

    Published in British journal of dermatology (1951) (01-06-2019)
    “…Summary Background Hidradenitis suppurativa (HS) is a rare, debilitating neutrophilic dermatosis characterized by chronic inflammation of hair follicles. Many…”
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    Lesional activation of T c 17 cells in Behçet disease and psoriasis supports HLA class I-mediated autoimmune responses by Vural, S, Kerl, K, Ertop Doğan, P, Vollmer, S, Puchta, U, He, M, Arakawa, Y, Heper, A O, Karal-Öktem, A, Hartmann, D, Boyvat, A, Prinz, J C, Arakawa, A

    Published in British journal of dermatology (1951) (01-12-2021)
    “…Behçet disease (BD) presents with lymphocytic and neutrophilic vasculitis of unknown aetiology. HLA-B*51, the endoplasmic reticulum aminopeptidase 1 (ERAP1),…”
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    Journal Article
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    多发性化脓性汗腺炎患者 pyrin 突变 by Vural, S., Gündoğdu, M., Gökpınar Ili, E., Durmaz, C.D., Vural, A., Steinmüller‐Magin, L., Kleinhempel, A., Holdt, L.M., Ruzicka, T., Giehl, K.A., Ruhi, H.I., Boyvat, A.

    Published in British journal of dermatology (1951) (01-06-2019)
    “…Summary 化脓性汗腺炎(HS)是一种炎性皮肤病, 在全世界约有1%HS患者。HS可使患者生活质量严重下降, 使腋窝和臀部等有毛发的部位出现慢性疼痛病变 (小块受累区域)。本次研究由土耳其和德国的科学家进行, 旨在分析 MEFV 基因在HS 中的作用, 研究使用了…”
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    Pyrin mutations in complex hidradenitis suppurativa by Vural, S., Gündoğdu, M., Gökpınar İli, E., Durmaz, C.D., Vural, A., Steinmüller‐Magin, L., Kleinhempel, A., Holdt, L.M., Ruzicka, T., Giehl, K.A., Ruhi, H.I., Boyvat, A.

    Published in British journal of dermatology (1951) (01-06-2019)
    “…Summary Hidradenitis suppurativa (HS) is an inflammatory skin disease affecting approximately 1% of people worldwide. HS can cause a severe decline in quality…”
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    Ulcerative IgA vasculitis in the setting of warfarin therapy by Kalay-Yildizhan, I, Akay, BN, Boyvat, A, Heper, A

    Published in Dermatology online journal (01-01-2020)
    “…Henoch-Schönlein purpura (HSP) is a small vessel vasculitis characterized by the presence of vascular immunoglobulin A deposition that usually presents as…”
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    Livedoid vasculopathy associated with heterozygous protein C deficiency by Boyvat, A., KundakC¸i, N., Babikir, M.O.A., Gürgey, E.

    Published in British journal of dermatology (1951) (01-10-2000)
    “…Livedoid vasculopathy is characterized by recurrent painful ulceration of the feet, ankles and legs that heals with residual white atrophic scars. For many…”
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    The prevalence of Behçet's disease above the age of 10 years The results of a pilot study conducted at the Park Primary Health Care Center in Ankara, Turkey by Idil, A., Gürler, A., Boyvat, A., Çaliskan, D., Özdemir, Ö., Isik, A., Tunçbilek, A., Koçyigit, P., Çalikoglu, E.

    Published in Ophthalmic epidemiology (01-12-2002)
    “…PURPOSE The aim of this study was to determine the prevalence of Behçet's disease above the age of 10 years by means of a population-based study. METHODS The…”
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    Soluble tumour necrosis factor receptors sTNFR1 and sTNFR2 are produced at sites of inflammation and are markers of arthritis activity in Behçet's disease by Turan, B., Pfister, K., Diener, P-A., Hell, M., Möller, B., Boyvat, A., Ergin, S., Villiger, P. M.

    “…Objective: We analysed the production of soluble tumour necrosis factor receptors sTNFR1 and sTNFR2 at sites of inflammation and measured their plasma…”
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    Behçet's disease-like presentation of bullous pyoderma gangrenosum associated with Crohn's disease by Akay, N., Boyvat, A., Heper, A. O., Soykan, I., Arica, I. E., Bektas, M., Ensari, A., Cokca, F.

    Published in Clinical and experimental dermatology (01-05-2006)
    “…Summary A 47‐year‐old woman presented with a 2‐month history of generalized arthralgia and a 10‐day history of oral aphthous ulcers. After hospitalization,…”
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    A case of pemphigus vulgaris possibly triggered by quinolones by Anadolu, RY, Birol, A, Bostanci, S, Boyvat, A

    “…Pemphigus vulgaris is an autoimmune blistering disorder in which both genetic and environmental factors, mainly drugs, are thought to play a part in its…”
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    Long-term effects of interferon alpha 2A treatment in Behçet's disease by Boyvat, A, Sişman-Solak, C, Gürler, A

    Published in Dermatology (Basel) (01-01-2000)
    “…Between May 1995 and April 1996, 20 patients with Behçet's disease were successfully treated with interferon alpha(2a) (IFN-alpha(2a)) 9 million IU/day three…”
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    Evaluation of clinical findings according to sex in 2313 Turkish patients with Behçet's disease by Tursen, Umit, Gurler, Aysel, Boyvat, Ayse

    Published in International journal of dermatology (01-05-2003)
    “…Background Behçet's disease is a multisystem disease featuring mucocutaneous, ocular, articular, vascular, intestinal, urogenital, and neurologic involvement…”
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    Interaction of commonly used emollients with photochemotherapy by Boyvat, Ayşe, Erdi, Hatice, Birol, Ahu, Gůrgey, Erbak

    “…Background/Aim: Even though emollients are commonly used in combination with photochemotherapy, we still lack guidance for the selection of the appropriate…”
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