Yazar "Darcan, Sukran" için listeleme
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PHENOTYPIC, HORMONAL AND MOLECULAR GENETIC CHARACTERISTICS OF 5-ALPHA REDUCTASE TYPE 2 DEFICIENCY PATIENTS: A MULTICENTER STUDY FROM TURKEY
Abaci, Ayhan; Catli, Gonul; Kirbiyik, Ozgur; Sahin, Nursel M.; Abali, Zehra Y.; Unal, Edip; Siklar, Zeynep; Ucakturk, Eda M.; Ozen, Samim; Guran, Tulay; Kara, Cengiz; Yildiz, Melek; Eren, Erdal; Nalbantoglu, Ozlem; Guven, Ayla; Cayir, Atilla; Akbas, Emine D.; Kor, Yilmaz; Curek, Yusuf; Aycan, Zehra; Bas, Firdevs; Darcan, Sukran; Berberoglu, Merih (KARGER, 2017)… -
Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort
Guran, Tulay; Buonocore, Federica; Saka, Nurcin; Ozbek, Mehmet Nuri; Aycan, Zehra; Bereket, Abdullah; Bas, Firdevs; Darcan, Sukran; Bideci, Aysun; Guven, Ayla; Demir, Korcan; Akinci, Aysehan; Buyukinan, Muammer; Aydin, Banu Kucukemre; Turan, Serap; Agladioglu, Sebahat Yilmaz; Atay, Zeynep; Abali, Zehra Yavas; Tarim, Omer; Catli, Gonul; Yuksel, Bilgin; Akcay, Teoman; Yildiz, Metin; Ozen, Samim; Doger, Esra; Demirbilek, Huseyin; Ucar, Ahmet; Isik, Emregul; Ozhan, Bayram; Bolu, Semih; Ozgen, Ilker Tolga; Suntharalingham, Jenifer P.; Achermann, John C. (ENDOCRINE SOC, 2016)Context: Primary adrenal insufficiency (PAI) is a life-threatening condition that is often due to monogenic causes in children. Although congenital adrenal hyperplasia occurs commonly, several other important molecular ...
