Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Esra Baǧlan"'
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 22, Iss 1, Pp 1-3 (2024)
Abstract Background Camurati-Engelmann disease (CED), also known as progressive diaphyseal dysplasia, is a rare genetic disorder characterized by abnormal thickening of the long bones’ diaphysis. This condition is caused by mutations in the transfo
Externí odkaz:
https://doaj.org/article/f4d5765224174621a16a0dfd3a8abe66
Autor:
Betül Sözeri, Nihal Şahin, Ceyhun Açarı, Pinar Ozge Avar Aydın, Ozge Baba, Esra Bağlan, Sevcan Bakkaloğlu, Sibel Bakırcı, Yelda Bilginer, Burcu Yücel Bozkaya, Şengül Çağlayan, Mustafa Çakan, Figen Çakmak, Taner Coşkuner, Ferhat Demir, Fatma Gül Demirkan, Şeyda Doğantan, Hatice Adıgüzel Dündar, Emine Duygu Ersözlü, Sercan Gücenmez, Oğuz Gürler, Rana İşgüder, Adem Küçük, Mukaddes Kalyoncu, Levent Kılıç, Sara Şebnem Kılıç, Hakan Kısaoğlu, Ayşenur Paç Kısaarslan, Zehra Kızıldağ, Duygu Kurtuluş, Semanur Özdel, Kübra Öztürk, Pelin Şenol, Ayşe Tanatar, Sema Nur Taşkın, Fatma Tuncer Kuru, Serkan Türkuçar, Kadir Ulu, Erbil Ünsal, Ayten Yazıcı, Deniz Gezgin Yıldırım, Selçuk Yüksel, Özgür Kasapçopur, Seza Özen, Nuray Aktay Ayaz, Hafize Emine Sönmez
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 22, Iss 1, Pp 1-8 (2024)
Abstract Background Juvenile idiopathic arthritis (JIA) is a prevalent childhood chronic arthritis, often persisting into adulthood. Effective transitional care becomes crucial as these patients transition from pediatric to adult healthcare systems.
Externí odkaz:
https://doaj.org/article/187d01c6145449ee8f1fa1689ec25482
Autor:
Kübra Öztürk, Taner Coşkuner, Esra Baglan, Hafize Emine Sönmez, Gülçin Otar Yener, Figen Çakmak, Fatma Gül Demirkan, Ayşe Tanatar, Serife Gül Karadag, Semanur Ozdel, Ferhat Demir, Mustafa Çakan, Nuray Aktay Ayaz, Betül Sözeri
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2022)
Familial Mediterranean fever (FMF) is the most common monogenic autoinflammatory disease manifesting phenotypic heterogeneity. It is a clinically diagnosed disease supported by MEditerranean FeVer (MEFV) gene mutation analysis. However, the phenotype
Externí odkaz:
https://doaj.org/article/5d8fa5f1045b4c338308262cb19881a0
Autor:
Şengül Çaǧlayan, Hafize Emine Sönmez, Gülçin Otar Yener, Esra Baǧlan, Kübra Öztürk, Kadir Ulu, Vafa Guliyeva, Demet Demirkol, Mustafa Çakan, Semanur Özdel, Hulya Bukulmez, Nuray Aktay Ayaz, Betül Sözeri
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
ObjectiveThe study aimed to report the efficacy and safety of anakinra treatment in patients with the refractory multisystemic inflammatory syndrome in children (MIS-C).MethodsThis is a cross-sectional retrospective study consisting of pediatric pati
Externí odkaz:
https://doaj.org/article/9799b46aea9747afb7a3d3c9a3e47979
Autor:
Semanur Ozdel, Hafize Emine Sönmez, Şengül Çağlayan, Özlem Akgün, Tuncay Aydın, Özge Baba, İlknur Bağrul, Gülçin Otar Yener, Kübra Öztürk, Ferhat Demir, Deniz Gezgin Yıldırım, Şerife Gül Karadağ, Esra Bağlan, Mustafa Çakan, Mukaddes Kalyoncu, Balahan Bora Makay, Şevket Erbil Ünsal, Sevcan Bakkaloğlu, Mehmet Bülbül, Betül Sözeri, Nuray Aktay Ayaz
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 21, Iss 1, Pp 1-7 (2023)
Abstract Objective Rheumatoid factor (RF)-positive polyarthritis is the least common type of juvenile idiopathic arthritis (JIA). Functional disability in RF-positive polyarthritis patients is much more severe than in patients with other subtypes; bu
Externí odkaz:
https://doaj.org/article/2f5221155e154e34b2c55c80b9572e80
Autor:
İlknur Bağrul, Serdar Ceylaner, Yasemin Tasci Yildiz, Serife Tuncez, Elif Arslanoglu Aydin, Esra Bağlan, Semanur Ozdel, Mehmet Bülbül
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 21, Iss 1, Pp 1-8 (2023)
Abstract Background Camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome, caused by biallelic pathogenic mutations in the proteoglycan 4 (PRG4) gene, is characterized by early-onset camptodactyly, noninflammatory arthropathy, coxa vara de
Externí odkaz:
https://doaj.org/article/587a329c76264d2ba6fb7b426a8ab58f
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