Zobrazeno 1 - 10
of 104
pro vyhledávání: '"Nihal ŞAHİN"'
Autor:
Cihan İnan, Lütfiye Uygur, Verda Alpay, Reyhan Ayaz, Nihal Şahin Uysal, Aydan Biri, Gökhan Yıldırım, Niyazi Cenk Sayın
Publikováno v:
Balkan Medical Journal, Vol 41, Iss 5, Pp 333-347 (2024)
Hypertensive disorders of pregnancy are significant contributors to maternal and perinatal morbidity and mortality. The definition, classification, and management of these disorders have evolved over time. Notably, the disease classification enables
Externí odkaz:
https://doaj.org/article/57915097fc434afc89b060fe283394e6
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:
Nihal ŞAHİN, Sevda ASADOVA, Sema Nur TAŞKIN, Şeyda DOĞANTAN, Sümeyra ÖZDEMİR ÇİÇEK, Ayşenur PAÇ KISAARSLAN, Hakan POYRAZOĞLU
Publikováno v:
Ahi Evran Medical Journal, Vol 7, Iss 3, Pp 288-295 (2023)
Purpose: Comorbidities are conditions that exist or occur during an index disease course. Comorbidities may affect the chronic disease process. Juvenile idiopathic arthritis (JIA) is a chronic childhood arthritis of unknown etiology. We aimed to eval
Externí odkaz:
https://doaj.org/article/1b8f9678806d40648e007a64cd0d13f6
Autor:
Sevda Asadova, Ayşenur Paç Kısaarslan, Sümeyra Özdemir Çiçek, Nihal Şahin, Sema Nur Taşkın, Şeyda Doğantan, Muammer Hakan Poyrazoğlu
Publikováno v:
The Journal of Pediatric Academy, Vol 3, Iss 3, Pp 95-103 (2022)
Introduction:It is essential to evaluate the activation and the articular and extra-articular damage during the Juvenile Idiopathic Arthritis(JIA) disease course. Objectives:This study aimed to evaluate the damage status and affecting factors in J
Externí odkaz:
https://doaj.org/article/c8794fba0cbe4784bb637dcad6fda1b3
Autor:
Merve Nur Tekin, Ruhan Düşünsel, Nihal Şahin, İsmail Dursun, Betül Sözeri, Sumeyra Özdemir Çiçek, Ayşenur Paç Kısaarslan, Muammer Hakan Poyrazoğlu
Publikováno v:
The Journal of Pediatric Academy, Vol 3, Iss 3, Pp 125-131 (2022)
Abstract Introduction and Objectives: Juvenile idiopathic arthritis (JIA) is a frequently seen chronic rheumatoid disease in childhood, which may cause disability and severely affect quality of life (QoL). The aim of present study was to assess re
Externí odkaz:
https://doaj.org/article/3061af59dce0450990170c0cde52b33b
Autor:
Ayşe Seda Pınarbaşı, Ismail Dursun, Burcu Daldaban, Neslihan Günay, Sümeyra Çiçek, Nihal Şahin, Sibel Yel, Muammer Hakan Poyrazoglu, Hülya Akgün, Ruhan Düşünsel
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 30, Iss 6, Pp 1450-1456 (2019)
Epidermolysis bullosa (EB) encompasses a clinically and genetically heterogeneous group of rare inherited diseases characterized by marked mechanical fragility of epithelial tissues with blistering and erosions following minor trauma. Amyloidosis is
Externí odkaz:
https://doaj.org/article/eefebc4de184462b9903827e5f22c970
Publikováno v:
Gynecology Obstetrics & Reproductive Medicine, Vol 22, Iss 3, Pp 165-167 (2016)
We herein describe a woman with two consecutive pregnancies affected by fetal nuchal cystic hygroma (CH) with a normal karyotype. A 33-year-old woman (gravidity 2, parity 1) was referred to us because of fetal hydrops. No consanguinity or Rh isoimmun
Externí odkaz:
https://doaj.org/article/5f64193d78f7401c96e6481e8e073dee
Publikováno v:
Gynecology Obstetrics & Reproductive Medicine, Vol 18, Iss 1 (2012)
To review nutritional therapy of hyperhomocysteinemia observed in Methylenetetrahydrofolate Reductase (MTHFR) gene polymorphisms. The researches and review articles about the subject has been read, investigated, compiled and integrated with our clini
Externí odkaz:
https://doaj.org/article/e3c31d8fdcdd4d35b9b84a62f6b43e9c
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Publikováno v:
In Journal of Gynecology Obstetrics and Human Reproduction February 2022 51(2)