Browsing by Author "Bereket, Abdullah"
Now showing items 1-7 of 7
-
Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome
Sari, Erkan; Bereket, Abdullah; Yesilkaya, Ediz; Bas, Firdevs; Bundak, Ruveyde; Aydin, Banu Kucukemre; Yuksel, Bilgin (Wiley, 2016)To evaluate the anthropometric features of girls with Turner syndrome (TS) at birth and presentation and the effect of karyotype on these parameters. Data were collected from 842 patients with TS from 35 different centers, ... -
The Etiology and Clinical Features of Non-CAH Gonadotropin-Independent Precocious Puberty: A Multicenter Study
Atay, Zeynep; Yesilkaya, Ediz; Erdeve, Senay Savas; Turan, Serap; Akin, Leyla; Eren, Erdal; Bereket, Abdullah (Endocrine Soc, 2016)Aim: The causes of gonadotropin-independent precocious puberty are diverse, and often have overlapping clinical and biochemical features. With the exception of congenital adrenal hyperplasia (CAH), disorders that cause ... -
Evaluation of therapeutics management patterns and glycemic control of pediatric type 1 diabetes mellitus patients in Turkey: A nationwide cross-sectional study
Hatun, Sukru; Demirbilek, Huseyin; Darcan, Sukran; Yuksel, Aysegul; Binay, Cigdem; Simsek, Damla Goksen; Bereket, Abdullah (Elsevier Ireland Ltd, 2016)Aims: To evaluate the management strategies, glycemic control and complications of pediatric type 1 diabetes mellitus (T1DM) patients in Turkey. Methods: Study included 498 patients with T1DM between the ages 1-18. Data ... -
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 ... -
Revisiting Classical 3 beta-hydroxysteroid Dehydrogenase 2 Deficiency: Lessons from 31 Pediatric Cases
Guran, Tulay; Kara, Cengiz; Yildiz, Melek; Bitkin, Eda C.; Haklar, Goncagul; Lin, Jen-Chieh; Bereket, Abdullah (Endocrine Soc, 2020)Context: The clinical effects of classical 3 beta-hydroxysteroid dehydrogenase 2 (3 beta HSD2) deficiency are insufficiently defined due to a limited number of published cases. Objective: To evaluate an integrated steroid ... -
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 ...
