Search Results - "Çimşit, Gülseren"

Evaluation of the atherogenic tendency of lipids and lipoprotein content and their relationships with oxidant–antioxidant system in patients with psoriasis by Vanizor Kural, Birgül, Örem, Asım, Çimşit, Gülseren, Yandı, Yunus Emre, Calapoǧlu, Mustafa

“…Background: Psoriasis is a common chronic and recurrent inflammatory skin disease that can occur due to abnormalities in essential fatty acid metabolism,…”
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Plasma homocysteine and its relationships with atherothrombotic markers in psoriatic patients by Vanizor Kural, Birgül, Örem, Asım, Çimşit, Gülseren, Uydu, Hüseyin Avni, Yandi, Yunus Emre, Alver, Ahmet

“…Background: Hyperhomocysteinemia may constitute an independent risk factor for cardiovascular disease and may promote atherothrombosis. Psoriasis is one of the…”
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Coexistence of Mayer-Rokitansky-Kuster-Hauser Syndrome and Neurofibromatosis Type I by Yayli, Savaş, Bahadir, Sevgi, Çimşit, Gülseren, Bozkaya, Hasan, İmamoğlu, Halil İbrahim, Kul, Sibel

“…Neurofibromatosis type 1 (NF-1) is the most frequently seen form of neurofibromatosis. The characteristic features of this disorder are caf´ au lait macules ,…”
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A case of juvenile subcorneal pustular dermatosis successfully treated with acitretin by Yaylı, Savaş, Bahadır, Sevgi, Alpay, Köksal, Çimşit, Gülseren, Reis, Abdülkadir

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A case of juvenile hyaline fibromatosis by YAYLI, Savaş, UNCU, Sibel, ALPAY, Köksal, YILDIZ, Kadriye, ÇIMŞIT, Gülseren, BAHADIR, Sevgi

“…ABSTRACT Juvenile hyaline fibromatosis (JHF) is a rare, autosomally‐recessive disease characterized by papulonodular skin lesions, soft tissue masses, joint…”
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The evaluation of autoantibodies against oxidatively modified low-density lipoprotein (LDL), susceptibility of LDL to oxidation, serum lipids and lipid hydroperoxide levels, total antioxidant status, antioxidant enzyme activities, and endothelial dysfunction in patients with Behçet’s disease by Örem, Asım, Yandi, Y.Emre, Vanizor, Birgül, Çimşit, Gülseren, Uydu, Hüseyin Avni, Malkoç, Meltem

“…Objectives: Behçet’s disease is a multisystem disorder characterized by a chronic inflammation including acute attacks and remission periods. Decreased enzyme…”
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Pyoderma Gangrenosum in Association with Juvenile Rheumatoid Arthritis by Yaylı, Savaş, Bahadır, Sevgi, Alpay, Köksal, Çimşit, Gülseren, Çobanoğlu, Ümit, Tosun, Mehmet

“…A 17‐year‐old girl presented with multiple, painful, erythematous blisters and ulcerated lesions on the shins and buttocks. She also had arthralgia. She had…”
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Effect of Plasma from Patients with Behçet’s Disease on the Production of Nitric Oxide in Cultured Human Umbilical Vein Endothelial Cells by Örem, Asım, Ertürk, Murat, Çimşit, Gülseren, Kural, Birgül Vanizor

“…Objective: To determine the effect of plasma from patients with Behçet’s disease (BD) on the production of nitric oxide (NO) in cultured human umbilical vein…”
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Relationship between lipid peroxidation and disease activity in patients with Behçet's disease by Örem, Asım, Efe, Hasan, Deǧer, Orhan, Çimşit, Gülseren, Uydu, Hüseyin Avni, Vanizor, Birgül

“…Behçet's disease is a chronic multi-systemic disorder which is characterized by a relapsing systemic inflammatory process. The alteration of lipid profile and…”
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Erythema dyschromicum perstans: Response to dapsone therapy by Bahadir, Sevgi, Çobanoglu, Ümit, Çimsit, Gülseren, Yayli, Savas, Alpay, Köksal

“…Erythema dyschromicum perstans (EDP) is a rare disorder characterized by asymptomatic, slowly progressive, ash‐gray macular pigmentation of the skin, which…”
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Toxic epidermal necrolysis treated with intravenous immunoglobulin and granulocyte colony-stimulating factor by KALYONCU, Mukaddes, CIMSIT, Gülseren, CAKIR, Murat, ÖKTEN, Aysenur

“…We report a case of toxic epidermal necrolysis who was successfully treated with intravenous immunoglobin and granulocyte colony-stimulating factor. He had…”
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Radiation port wart : A distinct cutaneous lesion after radiotherapy by GENC, Mine, YAVUZ, Melek, CIMSIT, Gülseren, COBANOGLU, Omit, YAVUZ, Aydin

“…LABELED BACKGROUND: Radiotherapy may cause common cutaneous side effects such as acute and chronic radiodermatitis and also rare skin conditions. A 42-year-old…”
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Plasma polymorphonuclear leukocyte elastase levels and its relation to disease activity in psoriasis by Örem, Asim, Deǧer, Orhan, Çimşit, Gülseren, Bahadir, Sevgi

“…Although some increased enzyme activities in PMN leukocytes isolated from the circulation of psoriatic patients have been previously described, none of these…”
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The significance of autoantibodies against oxidatively modified low-density lipoprotein (LDL) in patients with psoriasis by Örem, Asim, Çimşit, Gülseren, Değer, Orhan, Örem, Cihan, Vanizor, Birgül

“…Psoriasis is associated with changes in plasma lipid and lipoproteins, which may play a role in the development of occlusive vascular disease. The oxidation of…”
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Lp(a) lipoprotein levels as a predictor of risk for thrombogenic events in patients with Behçet's disease by Orem, A, Değer, O, Memiş, O, Bahadir, S, Ovali, E, Cimşit, G

“…OBJECTIVES--To investigate whether plasma levels of Lp(a) lipoprotein (Lp(a)) are predictors of defective fibrinolytic activity, leading to thrombosis, in…”
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Lipoid proteinosis: A case with ophthalmological and psychiatric findings by BAHADIR, Sevgi, ÇOBANOĞLU, Ümit, KAPICIOĞLU, Zerrin, KANDIL, Sema Tanrıöver, ÇIMŞIT, Gülseren, SöNMEZ, Müjgan, YAYLI, Savaş

“…ABSTRACT Lipoid proteinosis (LP) is an uncommon, recessively inherited disorder. The disease usually has its onset in the newborn period and is manifested by…”
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Woringer-Kolopp disease coexpressing CD4 and CD8 treated with radiation therapy: a case report by Zengin, Ahmet Yasar, Topkan, Erkan, Cimsit, Gülseren, Yildiz, Kadriye

“…We present an extremely rare case of Woringer-Kolopp disease with CD4+/CD8+ immunohistochemical features in a 27-year-old male patient, which involved the…”
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Congenital primary hypoparathyroidism presented with extensive cutaneous and subcutaneous calcifications by Aslan, Y, Gedik, Y, Okten, A, Aksoy, A, Cimşit, G, Ari, N

“…Congenital primary hypoparathyroidism is very rare in infancy. It may be isolated or associated with other developmental defects, arising from the third and…”
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A case of juvenile hyaline fibromatosis by YAYLI, Savaş, UNCU, Sibel, ALPAY, Köksal, YILDIZ, Kadriye, ÇIMŞIT, Gülseren, BAHADIR, Sevgi

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Lipoid proteinosis: A case with ophthalmological and psychiatric findings by BAHADIR, Sevgi, ÇOBANOĞLU, Ümit, KAPICIOĞLU, Zerrin, KANDIL, Sema Tanrıöver, ÇIMŞIT, Gülseren, SöNMEZ, Müjgan, YAYLI, Savaş

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