Browsing by Author "Türker Şener, Leyla"
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Carotid artery plaque structure in the context of symptomatic/asymptomatic nature of carotid artery stenosis
Öztaş, Didem Melis; Tanören Bilen, Bukem; Türker Şener, Leyla; Beyaz, Metin Onur; Ulukan, Mustafa Özer; Ünal, Orçun; Ünlü, Mehmet Burçin; Reis, Paulo Eduardo Ocke; Uğurlucan, Murat (Czech Society of Cardiology and Czech Society for Cardiovascular Surgery, 2021)Objective: In this paper, we examined the relationship between atherosclerotic plaque characteristics and symptomatic carotid artery disease. Material and methods: Twenty-two patients who underwent carotid endarterectomy ... -
Comparison of S gene mutations in patients with occult and chronic hepatitis B virus infection
Çakal, Bülent; Çavuş, Bilger; Atasoy, Alp; Altunok, Damla; Poda, Mehveş; Bulakçı, Mesut; Gülluoğlu, Mine; Demirci, Mehmet; Türker Şener, Leyla; Arslan, Aslı Berru; Arıkan, Muzaffer; Akyüz, Filiz (Elsevier B.V., 2022)Background and aim: This study aimed to detect mutations in the HBV S gene and evaluate their relationship to occult hepatitis B virus (HBV) infection (OBI). Methods: The study included 32 patients with negative serum HBsAg ... -
Hereditary spherocytosis associated with defects of human red blood cell membrane
Albeniz, Işıl; Türker Şener, Leyla; Albeniz, Gürcan; Aktan, Melih; Üstek, Duran (Wiley-Blackwell, 2015)... -
Identification of red blood cell membrane defects in a patient with hereditary spherocytosis using next-generation sequencing technology and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
Türker Şener, Leyla; Aktan, Melih; Albeniz, Gürcan; Şener, Aziz; Üstek, Duran; Albeniz, Işıl (Spandidos Publ Ltd, 2019)Hereditary spherocytosis (HS) is characterized by the morphological transformation of erythrocytes into a spherical shape due to a hereditary defect in cell membrane proteins (ghosts) associated with disruption of erythrocyte ...
