Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Evra ÇELİKKAYA"'
Autor:
Esra Bağlan, Semanur Özdel, Tülin Güngör, Deniz Karakaya, Evra Çelikkaya, Fatma Yazılıtaş, Evrim Kargın Çakıcı, Mehmet Bülbül
Publikováno v:
The Journal of Pediatric Academy, Vol 2, Iss 3, Pp 101-105 (2021)
ABSTRACT Objectives: Behçet’s disease (BD) is a multisystemic inflammatory disease with unknown etiology. It is characterized by recurrent oral and genital ulcerations, uveitis, and skin lesions, various musculoskeletal, gastrointestinal, centr
Externí odkaz:
https://doaj.org/article/413ae57251fc4e85873abea5dd28a061
Autor:
Deniz KARAKAYA, Fatma YAZILITAŞ, Evrim KARGIN ÇAKICI, Tülin GÜNGÖR, Evra ÇELİKKAYA, Mehmet BÜLBÜL
Publikováno v:
Turkish Journal of Pediatric Disease. :1-6
Objective: Membranous nephropathy (MN) is a rare immune complex disease in pediatric population then adults. The prognosis of MN is variable, ranging from spontaneous complete remission to end-stage renal disease (ESRD). The lack of large multicenter
Autor:
Fatma Yazılıtaş, Evrim Kargın Çakıcı, Ayse Secil Eksioglu, Tülin Güngör, Evra Çelikkaya, Deniz Karakaya, Çiğdem Üner, Mehmet Bülbül
Publikováno v:
Hospital Practice. 51:82-88
Anxiety and depression in children with primary monosymptomatic nocturnal enuresis and their mothers
Autor:
Fatma Yazilitaş, Burak Açikel, Evrim Kargin Çakici, Tülin Güngör, Evra Çelikkaya, Fehime Kara Eroğlu, Deniz Karakaya, Gökçe Can, Eda Didem Kurt Şükür, Mehmet Bülbül
Publikováno v:
Children's Health Care. :1-10
Autor:
Deniz Karakaya, Tülin Güngör, Evrim Kargın Çakıcı, Fatma Yazılıtaş, Evra Çelikkaya, Mehmet Bülbül
Background Nephrotic syndrome is the most common glomerular disorder of childhood and data on complications are still limited and predisposing risk factors have not been fully defined. The aim of our study is to systematically evaluate treatment and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5eb2a01b5581877e830e66a7c054bc29
https://doi.org/10.21203/rs.3.rs-2864783/v1
https://doi.org/10.21203/rs.3.rs-2864783/v1
Autor:
Evra, Çelikkaya, Tülin, Güngör, Deniz, Karakaya, Evrim, Kargın Çakıcı, Fatma, Yazılıtaş, Fatih, Özaltın, Mehmet, Bülbül
Publikováno v:
Experimental and Clinical Transplantation. 20:45-48
Membranoproliferative glomerulonephritis and renal microangiopathies may manifest similar clinical presentations and histology. Many genetic mutations that cause these diseases have been reported. Studies on mutations in the gene encoding diacylglyce
Autor:
Tülin Güngör, Evrim Kargın Çakıcı, Fatma Yazılıtaş, Deniz Karakaya, Evra Çelikkaya, Mehmet Bülbül
Publikováno v:
Therapeutic Apheresis and Dialysis. 27:66-72
The objective of this study was to determine the common indications of acute intermittent hemodialysis (IHD) treatment in childhood and to assess the characteristics of the procedure, complications, and prognosis.The study included 102 patients aged
Autor:
Ulku Guler, Muzaffer Yildirim, Volkan Yazar, Deniz Karakaya, Tugce Yildirim, Eda Çiftci Dede, Fehime Kara Eroglu, Ihsan Gursel, Tülin Güngör, Evra Çelikkaya, Nilsu Turay, Mehmet Bülbül, Petek Korkusuz, Bekir Salih
Publikováno v:
American Journal of Physiology: Renal Physiology
Since previous research suggests a role of a circulating factor in the pathogenesis of steroid-sensitive nephrotic syndrome (NS), we speculated that circulating plasma extracellular vesicles (EVs) are a candidate source of such a soluble mediator. He
Autor:
Esra Bağlan, Deniz Karakaya, Fatma Yazılıtaş, Evrim Kargın Çakıcı, Mehmet Bülbül, Semanur Özdel, Tülin Güngör, Evra Çelikkaya
Publikováno v:
Journal of Pediatric Hematology/Oncology. 44:e413-e417
Henoch-Schonlein purpura (HSP) is the most common childhood systemic vasculitis. The present study aims to investigate the effectiveness of the immature granulocyte (IG) percentage as a new marker for predicting internal organ involvement in HSP. Thi
Publikováno v:
Aktuelle Rheumatologie. 47:152-157
Objective Systemic juvenile idiopathic arthritis is one of the subtypes of juvenile idiopathic arthritis. This type of disease accounts for approximately 10–20% of all cases of juvenile idiopathic arthritis. It typically affects both sexes equally