Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Betül Orhan Kiliç"'
Autor:
Betül Orhan Kiliç, Eda Çakmak
Publikováno v:
Ķazaķstannyṇ Klinikalyķ Medicinasy, Vol 20, Iss 5, Pp 42-46 (2023)
Objective: This study explores the relationships between sleep disorders, depressive symptoms, and obesity among children of different ages. Material and methods: The data for this study were collected from 163 Turkish children aged 7 to 10 and 11 to
Externí odkaz:
https://doaj.org/article/7e9679f15c8a45a4a3814295bf583c76
Autor:
Betül ORHAN KILIÇ, Serhat KILIÇ, Eylem GÜL ATEŞ, Abduljabar ADI, Sami DALATİ, Luai SHAABAN, Efe SEVİM, Dilek KONUKSEVER
Publikováno v:
Turkish Journal of Pediatric Disease. :1-6
Amaç: Çocukluk çağı obezitesi günümüzde en yaygın halk sağlığı sorunu haline gelmiştir. Çocukluk obezitesi için obezojenik aile uygulamaları, çocuk obezitesi ve depresif belirtiler arasındaki ilişkiyi incelemeyi amaçladık. Gere
Publikováno v:
Turkiye Klinikleri Journal of Pediatrics. 30:212-218
Publikováno v:
Hematology. 26:1013-1017
Vitamin B12 deficiency is a cause of preventable growth and developmental retardation in children. In this respect, alternative methods such as oral and sublingual treatments are being tried. We aimed to compare the efficacy of oral, sublingual, and
Publikováno v:
Genel Tıp Dergisi, Vol 33, Iss 4, Pp 390-393 (2023)
Objective: COVID-19-related lockdown decreased the children's exposure to sunlight, and they were susceptible to 25-hydroxyvitamin D [25(OH)D] deficiency. The present study aimed to examine the 25(OH)D levels 2 years before and during the first year
Externí odkaz:
https://doaj.org/article/973daadd01094ad3a43ada024292cb57
Autor:
Vesile Deniz Çelik, Betul Orhan Kiliç, Yasemin Ardiçoğlu Akişin, Fatma Ajlan Tükün, Nejat Akar
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 19, Iss 4, Pp 433-435 (2018)
Background: Hereditary hemochromatosis is a disease associated with iron deposition which is caused by the mutations in “hereditary Fe (iron)” (HFE) gene. Case: The 16-year-old male patient was diagnosed with hereditary hemochromatosis after c.10
Externí odkaz:
https://doaj.org/article/7f7585854dfa4a28a2330421b259fb83
Autor:
Kiliç BO; Department of Pediatrics, Baskent University Faculty of Medicine, Ankara, Turkey. Correspondence to: Dr. Betül Orhan Kiliç, Department of Pediatrics, Baskent University Faculty of Medicine, Ankara, Turkey. betulorhandr@hotmail.com., Konuksever D; Department of Pediatrics, Turkish Ministry of Health Ankara Bilkent City Hospital, Ankara, Turkey., Özbek NY; Division of Pediatric Hematology, Department of Pediatrics, University of Health Sciences, Ankara City Hospital, Ankara, Turkey.
Publikováno v:
Indian pediatrics [Indian Pediatr] 2024 Jul 15; Vol. 61 (7), pp. 621-626. Date of Electronic Publication: 2024 Apr 22.