Zobrazeno 1 - 10
of 19
pro vyhledávání: '"M. L. Ocal"'
A single center survey study of systemic vasculitis and COVID-19 during the first months of pandemic
Autor:
Ahmet Gül, D. Y. Guzey, B. F. Agargun, Bahar Artım Esen, Nevzat Koca, Sibel Zarali, M. Bektaş, Mehmet Salih Sevdi, M. L. Ocal, Murat Inanc, B. Ince, Ayse Ince, Yasemin Yalcinkaya
Publikováno v:
TURKISH JOURNAL OF MEDICAL SCIENCES. 51:2243-2247
INTRODUCTION: COVID-19 pandemic created concerns among patients receiving immunosuppressive therapy. Frequency of COVID-19 and impact of lockdown on treatment compliance in patients with vasculitis are largely unknown. PATIENTS AND METHOD: Patients w
Autor:
Murat Inanc, Yasemin Yalcinkaya, M. L. Ocal, B. F. Agargun, Gulcin Yegen, Ege Sinan Torun, Ahmet Gül, Meliha Nalcaci, Yunus Çatma, M. Bektaş, Bahar Artım Esen, Selman Fatih Beşişik
Publikováno v:
JCR: Journal of Clinical Rheumatology. 27:S639-S640
Publikováno v:
Abstracts Accepted for Publication.
Background: BAFF and APRIL are cytokines involved in B cell development and they take place in the pathogenesis of SLE. Objectives: The aim of this study was to investigate the relationship between serum BAFF/APRIL levels with clinical features and d
Autor:
B. Ince, Ahmet Gül, M. L. Ocal, Bahar Artim-Esen, Yeliz Ogret, Murat Inanc, Sevil Kamali, Fatma Oguz
Publikováno v:
Abstracts Accepted for Publication.
Background ANCA associated vasculitides (AAV) comprise an important subset of small vessel vasculitides with a multifactorial pathogenesis, which is considered to be associated with the interaction of genetic and environmental factors. Certain HLA Cl
Autor:
Bahar Artim-Esen, M. L. Ocal, R. Deniz, Murat Inanc, M. Erdugan, Yasemin Yalcinkaya, Ahmet Gül, Nizameddin Koca
Publikováno v:
Annals of the Rheumatic Diseases. 80:1006.2-1007
Background:Retinol binding protein 4 (RBP4) is a plasma retinol transporter that transports retinol from liver to periphery. RBP4 has been studied as a biomarker in metabolic and neoplastic conditions, however its association with inflammation is not
Autor:
Ahmet Gül, E. G. Işik, Bahar Artim-Esen, Yasemin Yalcinkaya, Murat Inanc, M. L. Ocal, B. Ince, Z. G. Özkan
Publikováno v:
Annals of the Rheumatic Diseases. 80:1210.2-1211
Background:Positron emission tomography (PET/CT) has gained importance in the diagnosis and assessment of large vessel vasculitis (LVV) recently.Objectives:We aimed to investigate the diagnostic importance and clinical significance of PET/CT findings
AB0331 PULMONARY INVOLVEMENT IN A SINGLE CENTER COHORT OF PATIENTS WITH SYSTEMIC LUPUS ERYTHEMATOSUS
Autor:
Ahmet Gül, M. Aydogan, Bahar Artim-Esen, Murat Inanc, E. Kocasoy-Orhan, E. Kiyan, A. Demir, Yasemin Yalcinkaya, N. Senkal, M. L. Ocal
Publikováno v:
Annals of the Rheumatic Diseases. 80:1191.1-1191
Background:The prevalence of SLE pulmonary involvement varies depending on several factors, including diagnostic methods [1].Objectives:We aimed to determine the frequency of involvement with different diagnostic methods in a single center cohort.Met
Autor:
Bahar Artim-Esen, Murat Inanc, Yasemin Yalcinkaya, Ahmet Gül, M. L. Ocal, B. Ince, M. Bektaş, B. Çelik
Publikováno v:
Annals of the Rheumatic Diseases. 80:282.3-283
Background:Psoriatic arthritis (PsA) is a heterogeneous disease and GRAPPA have proposed Minimal disease activity (MDA) as a composite outcome measure and has been validated in PsA.Objectives:In this study, we aimed to evaluate the characteristics, M
Autor:
Nizameddin Koca, Ahmet Gül, B. Ince, E. Oguz, Bahar Artim-Esen, Murat Inanc, C. Cetin, M. Bektaş, M. L. Ocal, Yasemin Yalcinkaya
Publikováno v:
Annals of the Rheumatic Diseases. 80:1409.3-1410
Background:Systemic AA amyloidosis is a serious and life-threatening complication of chronic inflammatory diseases such as rheumatoid arthritis, spondyloarthritis (SpA), and periodic fever syndromes. While most common cause of AA amyloidosis is Famil
Autor:
Bahar Artim-Esen, Murat Inanc, Yasemin Yalcinkaya, M. L. Ocal, Ahmet Gül, C. Cetin, Selma Sarı, B. Ince, B. Ç. Yalçin Dulundu, M. Bektaş, Nizameddin Koca
Publikováno v:
Annals of the Rheumatic Diseases. 80:951.3-952
Background:Familial Mediterranean fever (FMF) is a hereditary autoinflammatory disorder caused by the MEFV gene variants. Although association between FMF and spondyloarthritis (SpA) has previously been reported, clinical and laboratory features of p