Yazar "Guran, Tulay" için listeleme

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Evaluation of molecular characteristics and steroid metabolomics in a large cohort of children with 3 beta-hydroxysteroid dehydrogenase 2 deficiency

Guran, Tulay; Kara, Cengiz; Yildiz, Melek; Bitkin, Eda C.; Haklar, Goncagul; Lin, Jen-Chieh; Alkan, Afra (Karger, 2019)

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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. ...
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 ...