Browsing by Author "Dökmetaş H.S."
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Adrenal ganglioneuroma: Case report [Adrenal Ganglionöroma: Olgu Sunumu]
Kiliçli F.; Acibucu F.; Dökmetaş H.S.; Elagöz S.; Gökçe G.; Öztoprak I. (2011)Ganglioneuroma (GN) is a rare benign tumor arising mainly from neural crest cells and consisting of Schwann and ganglion cells. GN rarely occurs from the adrenal medulla and is observed most commonly in children and young ... -
Three cases with inappropriate TSH syndrome [Uygunsuz TSH sendromlu üç olgu]
Dökmetaş H.S.; Kiliçli F.; Acibucu F. (2012)Inappropriate thyroid-stimulating hormone (TSH) syndrome or central hyperthyroidism is a rare disorder characterized by inappropriately normal or elevated levels of TSH and elevated levels of T3 and T4. The syndrome is ... -
Two adult patients with ectopic neurohypophysis and panhypopituitarism due to absent pituitary stalk [Hipofiz sapı yokluğuna bağlı hipofizer yetmezliği ve ektopik nörohipofizi olan İki erişkin]
Acıbucu F.; Kılıçlı F.; Dökmetaş H.S. (2014)We report two cases of 27-year-old and 19-year-old female patients with ectopic neurohypophysis and panhypopituitarism due to absent pituitary stalk. They were admitted to the endocrinology clinic with short stature, growth ...