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Başlık için Tıp Fakültesi listeleme

Başlık için Tıp Fakültesi listeleme

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  • Bayındır, Tuba; Karadağ, Neşe; Karataş, Erkan; Kızılay, Ahmet (Kulak Burun Bogaz Ihtis Derg., 2013)
    Neuroendocrine tumors of the larynx are rarely seen neoplasms. Atypical carcinoid tumor is the most common type of the neuroendocrine tumors of the larynx, whereas the typical carcinoid tumor is the most infrequent ...
  • Kaplan, Yüksel; Kamışlı, Özden; Altınayar, Sibel; Özcan, Abdulcemal (Noro Psikiyatri Arsivi, 2015)
    Introduction: Few studies have reported the predictive factors related to mortality in patients with cranio-cervical artery dissections (CCAD). Our aim was to investigate the predictors related to in-hospital mortality ...
  • Kuku, İrfan (Elsevıer ıreland ltd, elsevıer house, brookvale plaza, east park shannon, co, clare, 00000, ıreland, 2018)
    Background and aims: Familial hypercholesterolemia (FH) is a common genetic disease of high-level cholesterol leading to premature atherosclerosis. One of the key aspects to overcome FH burden is the generation of largescale ...
  • Dikci, Seyhan; Ceylan, Osman Melih; Demirel, Soner; Yılmaz, Turgut (Consel brasıl oftalmologıa, alameda santos 1343, 11 andar cj 1110, cerqueıra cesar, sao paulo, sp 00000, brazıl, 2018)
    Purpose: To compare 0.5 mg and 0.625 mg of bevacizumab for treating aggressive posterior retinopathy of prematurity (AP-ROP). Methods: The medical records of patients with AP-ROP who were administered intravitreal bevacizumab ...
  • Karaman, Abdurrahman; Şamdancı, Emine; Doğan, Metin; Aksoy, Rauf Tuğrul; Sığırcı, Ahmet; Demircan, Mehmet (Urology, 2011)
    Xanthogranulomatous pyelonephritis is a chronic renal inflammation characterized by destruction and replacement of its parenchyma with granulomatous tissue. This uncommon condition is rare in children. We report on a ...
  • Yılmaz, E.; Çelik, Ö.; Türkçüoğlu, I.; Şimşek, Y.; Karaer, A.; Otlu, Barış; Gülbay, G.; Yeşilada, E. (European Review for Medical and Pharmacological Sciences, 2012)
    The purpose of the present study was to identify the role of abnormalities in DNA repair pathways by measuring the XPD and XRCC1 gene polymorphisms. MATERIALS AND METHODS: Thirty-five patients with abnormal cervical ...