A5082265886- Inflammasome and immune disorders
- Vasculitis and related conditions
- Gout, Hyperuricemia, Uric Acid
- Dermatological and COVID-19 studies
- Salivary Gland Disorders and Functions
- Kawasaki Disease and Coronary Complications
- Urticaria and Related Conditions
- Systemic Lupus Erythematosus Research
- Cholesterol and Lipid Metabolism
- Autoimmune Bullous Skin Diseases
- Infectious Diseases and Tuberculosis
- Spondyloarthritis Studies and Treatments
- Salivary Gland Tumors Diagnosis and Treatment
- interferon and immune responses
- Ocular Diseases and Behçet’s Syndrome
- Renal Diseases and Glomerulopathies
- Sarcoma Diagnosis and Treatment
- Cerebrovascular and Carotid Artery Diseases
- Atherosclerosis and Cardiovascular Diseases
- IL-33, ST2, and ILC Pathways
- Rheumatoid Arthritis Research and Therapies
- IgG4-Related and Inflammatory Diseases
- Case Reports on Hematomas
- Heparin-Induced Thrombocytopenia and Thrombosis
- COVID-19 Clinical Research Studies
Eskişehir City Hospital
2020-2024
Sağlık Bilimleri Üniversitesi
2023-2024
Eskişehir Osmangazi University
2018-2021
Center for Rheumatology
2020-2021
Eskişehir Osmangazi Üniversitesi Tıp Fakültesi Hastanesi
2019-2021
Dicle University
2014-2015
Abstract The objective of this study was to assess the pregnancy outcomes in a cohort patients who experienced pregnancies before and/or after being diagnosed with Takayasu’s arteritis (TA). present investigation encompassed total 88 seen 35 met criteria outlined by American College Rheumatology 1990 for classification Takayasu Pregnancies were classified into two categories. 1. that occurred diagnosis (pre-d or pre-TA) 2. happened following (post-d post-TA). Fifty-nine (67.0%) 21 TA and...
Persistent inflammation is an insidious and less studied feature of FMF. We investigated clinical determinants persistent its associations with individual damage items.This a cross-sectional analysis 917 FMF patients, who fulfilled the Tel Hashomer criteria had at least 6 months' follow-up. Patients were stratified based on whether they inflammation. used logistic regression to investigate independent predictors associated items.One hundred forty-two (15%) patients Active (54%) was most...
The course of novel coronavirus disease 2019 (COVID-19) has been special concern in patients with inflammatory rheumatic diseases (IRDs) due to the immune dysregulation that may be associated these and medications used for IRDs, affect innate responses.In this cohort study, we aimed report characteristics variables COVID-19 outcome among Turkish IRDs.Between April June, 2020, 167 adult IRD were registered from 31 centers 14 cities Turkey. Disease was classified 4 categories; (i) outpatient...
Background/aim: Colchicine is the mainstay of treatment in FMF. However, daily practice it not easy to maintain effective colchicine doses a substantial number patients due its side effects. In this study, we aimed investigate prevalence and risk factors for effects that limit optimal drug dosing cause permanent discontinuation. Materials methods: All were recruited from "FMF Central Anatolia" (FiCA) cohort, 915 adults with minimum follow-up time 6 months during which they had obeyed all...
This study aimed to describe the clinical spectrum of primary Sjögren's syndrome (pSS) patients with anti-Ro/SS-A and anti-La/SS-B negativity.
This study aimed to determine the specific characteristics of extraglandular manifestations especially cutaneous involvement in patients with primary sjögren’s syndrome(pSS), focusing on different clinical and histologic types SS-associated vasculitis. A retrospective was conducted 402 (378 women 24 men) pSS were analyzed. Patients categorized into three subgroups based serological tests. These; 1) quadruple seropositive (positive for anti-Sjögren’s-syndrome-related antigen antibodies...
Familial Mediterranean Fever (FMF) is the prototype of hereditary autoinflammatory disorders and caused by mutations on MEFV gene located short arm chromosome 16. Although some variants are clearly associated with disease phenotype, there numerous unknown clinical association which termed as uncertain significance (VUS). Here, we present correlations VUS in a large cohort adult FMF patients from three tertiary centers Central Anatolia.All were recruited Anatolia (FiCA) cohort. Demographic...
Familial Mediterranean fever (FMF), is an auto-inflammatory disease characterized by attacks of and serositis. Some scoring systems have been developed to evaluate the severity disease, however, predicting FMF not possible with current knowledge. Our aim in this study was factors affecting FMF.This included 150 patients. The medical data patients were collected retrospectively International system for (ISSF) used severity.Patients sorted into 3 groups based on ISSF scores; ≤2=mild (Group 1;...
Objectives: Familial Mediterranean fever (FMF) is the most common hereditary auto-inflammatory disease.Our aim in current study was to evaluate relation between gender and clinical findings, severity of disease treatment compliance FMF patients.Materials Methods: Medical records 150 patients were retrospectively evaluated.Disease scores evaluated with international score system for familial (ISSF), six-item modified Morisky scale compared males females.Results: Of patients, 87 (58 %) female...
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Single-organ cutaneous small-vessel vasculitis (SoCSVV) is an inflammatory skin-limited vascular disease affecting the dermal and/or hypodermal vessel wall. Pathogenetically, idiopathic forms are described, as well induction from different triggers, such infections, drugs, and vaccines. Following Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) pandemic outbreak, cases of induced by both COVID-19 vaccinations have been reported in literature. The aim this study to provide most...
Objective: The clinical burden of gouty arthritis has historically been well recognized; however, gout is often misdiagnosed and mismanaged. In this study, we aimed to evaluate the diagnoses treatments given patients admitted different specialties. Methods: Patients who were diagnosed with attacks treated by a rheumatologist included, while other non-gout rheumatic diseases (connective tissue diseases, rheumatoid arthritis, spondyloarthropathies, calcium pyrophosphate disease, etc.)...
Sjögren's syndrome (SS) is an autoimmune disease characterized by heterogeneous clinical presentation and the presence of various autoantibodies. This study aimed to determine differences in findings according antibody positivity patients with primary Sjögren (pSS) Turkish population. A retrospective was conducted 402 (378 women 24 men) pSS were analyzed. The categorized into three subgroups based on serological tests. These (1) quadruple seropositivity (positive for anti-Sjögren's...
<h3>Background:</h3> Uveitis is the most common extra-articular feature of spondyloarthritis (SpA). Sometimes uveitis may be only clinical finding SpA leading to diagnosis. In current literature, there information about frequency and characteristics in patients; however, factors associated with are not clear(1,2). <h3>Objectives:</h3> Our aim this study was analyze uveitis-related a large cohort patients. <h3>Methods:</h3> This multicenter, prospective observational used TReasure database...
Cansu, Döndü Üsküdar MD; Bodakçi, Erdal Canaz, Funda Çalişir, Cüneyt Korkmaz, Cengiz MDAuthor Information
McCune-Albright sendromu, poliostotik fibröz displazi, deride kahverenginde lekelenme (Cafe au lait lekeleri) ve otonomik
Leukemoid reaction is characterized by an elevation in neutrophil levels peripheral blood and defined as a total leukocyte number exceeding 50,000/mm 3 .An increase mature neutrophils occurs reaction.A 70-year-old man was referred to us due development of leukocytosis.His history revealed that the mass had begun beneath armpit 2 months previously spread rapidly.At physical examination his general condition poor, he conscious, oriented cooperative.Yellow-colored, painful, ulcerated necrotized...