Yazar "0000-0001-5715-4244" için Araştırma Çıktıları | TR-Dizin | WoS | Scopus | PubMed listeleme
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Difficulties in the diagnosis of Hb S/Beta thalassemia: Really a mild disease?
Uçucu, Süheyl; Karabıyık, Talha; Azık, Fatih Mehmet (SOC MEDICAL BIOCHEMISTS SERBIA, 2022)Background: HbS/beta cases having clinical, hematologic and electrophoretic similarities cannot be sufficiently distinguished from sickle cell anemia cases and are misdiagnosed as sickle cell anemia. This study will ... -
The effect of measurement area size on the reliability of myocardial iron load measurement in cardiac magnetic resonance imaging examinations of thalassemia patients
Yeniçeri, İbrahim Önder; Azık, Fatih Mehmet; Elibol, Funda Dinç (Turkiye Klinikleri, 2021)Background/aim: The aim of this study was to evaluate the intraobserver and interobserver reliability of cardiac T2* MRI measurements in different region of interest (ROI) sizes. Materials and methods: Cardiac T2* MRIs of ... -
IVS-II-16 (G>C) (HBB: c.315+16G>C) or IVS-II-666 (C>T) (HBB: c.316-185C>T) Mutations Trigger an Hb S (HBB: c.20A>T)/β+-Thalassemia Phenotype in an Hb S Trait Patient
Uçucu, Süheyl; Karabıyık, Talha; Azık, Fatih Mehmet (Taylor and Francis Ltd., 2021)Sickle cell trait is a medical condition caused by the presence of both mutant Hb S (HBB: c.20A>T) and normal Hb A alleles. Although sickle cell trait is typically considered to be asymptomatic and benign, genetic modifiers ...