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Evaluation of diagnosis and treatment results in children with Graves' disease with emphasis on the pubertal status of patients.
Poyrazoğlu S, Saka N, Bas F, Isguven P, Dogu A, Turan S, Bereket A, Sarikaya S, Adal E, Cizmecioglu F, Saglam H, Ercan O, Memioglu N, Günöz H, Bundak R, Darendeliler F, Yildiz M, Guran T, Akcay T, Akin L, Hatun S. Poyrazoğlu S, et al. J Pediatr Endocrinol Metab. 2008 Aug;21(8):745-51. doi: 10.1515/jpem.2008.21.8.745. J Pediatr Endocrinol Metab. 2008. PMID: 18825874
Distribution of gene mutations associated with familial normosmic idiopathic hypogonadotropic hypogonadism.
Gürbüz F, Kotan LD, Mengen E, Şıklar Z, Berberoğlu M, Dökmetaş S, Kılıçlı MF, Güven A, Kirel B, Saka N, Poyrazoğlu Ş, Cesur Y, Doğan M, Özen S, Özbek MN, Demirbilek H, Kekil MB, Temiz F, Önenli Mungan N, Yüksel B, Topaloğlu AK. Gürbüz F, et al. Among authors: poyrazoglu s. J Clin Res Pediatr Endocrinol. 2012 Sep;4(3):121-6. doi: 10.4274/jcrpe.725. Epub 2012 Jul 5. J Clin Res Pediatr Endocrinol. 2012. PMID: 22766261 Free PMC article.
125 results