Browsing by Author "Darendeliler, Feyza"
Now showing items 1-5 of 5
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A Comprehensive Online Calculator for Pediatric Endocrinologists: CEDD Cozuum/TPEDS Metrics
Demir, Korcan; Ozen, Samim; Konakci, Ergun; Aydin, Murat; Darendeliler, Feyza (Galenos Yayincilik, 2017)… -
The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study
Siklar, Zeynep; Genens, Mikayir; Poyrazoglu, Sukran; Bas, Firdevs; Darendeliler, Feyza; Bundak, Ruveyde; Cayir, Atilla (Galenos Yayincilik, 2016)Objective: Noonan syndrome (NS) is a multisystem disorder, and short stature is its most striking manifestation. Optimal growth hormone (GH) treatment for NS is still controversial. In this study, using a nationwide ... -
Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group
Darendeliler, Feyza; Yesilkaya, Ediz; Bereket, Abdullah; Bas, Firdevs; Bundak, Ruveyde; Sari, Erkan; Goksen, Damla (Galenos Yayincilik, 2015)Objective: Children with Turner syndrome (TS) have a specific growth pattern that is quite different from that of healthy children. Many countries have population-specific growth charts for TS. Considering national and ... -
Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38,935 Infants
Guran, Tulay; Tezel, Basak; Gurbuz, Fatih; Eklioglu, Beray Selver; Hatipoglu, Nihal; Kara, Cengiz; Darendeliler, Feyza (Galenos Yayincilik, 2019)Objective: Congenital adrenal hyperplasia (CAH) is the most common form of primary adrenal insufficiency in children. Neonatal screening for CAH is effective in detecting the salt-wasting (SW) form and in reducing mortality. ... -
Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study
Yesilkaya, Ediz; Bereket, Abdullah; Darendeliler, Feyza; Bas, Firdevs; Poyrazoglu, Sukran; Aydin, Banu Kucukemre; Tarim, Omer (Galenos Yayincilik, 2015)Objective: Turner syndrome (TS) is a chromosomal disorder caused by complete or partial X chromosome monosomy that manifests various clinical features depending on the karyotype and on the genetic background of affected ...
