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The Turkish Journal of Pediatrics|February 6, 2008
The validity of pallor as a clinical sign of anemia in cases with beta-thalassemiaS Songül Yalçin, Selma Unal, Fatma Gümrük, et al.
Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology|October 21, 2014
Survey of Hfe Gene C282Y Mutation in Turkish Beta-Thalassemia Patients and Healthy Population: A Preliminary StudySelma Unal, Günay Balta, Fatma Gümrük, et al.
Pediatric Hematology and Oncology|July 16, 2005
Prothrombin G20210A mutation in Turkish children with thrombosis and the frequency of prothrombin C20209TAytemiz Gurgey, Selma Unal, Hamza Okur, et al.
American Journal of Hematology|August 13, 2004
Five Fanconi anemia patients with unusual organ pathologiesSelma Unal, Namik Ozbek, Abdurrahman Kara, et al.
Journal of Pediatric Hematology/Oncology|January 10, 2009
Significance of fetal hemoglobin values in detection of heterozygotes in fanconi anemia: reevaluation of fetal hemoglobin values by a sensitive methodFatma Gumruk, Betul Tavil, Gunay Balta, et al.
Pediatric Hematology and Oncology|February 25, 2011
Evaluation of the psychological problems in children with sickle cell anemia and their familiesSelma Unal, Fevziye Toros, Meryem Özlem Kütük, et al.
Journal of Pediatric Hematology/Oncology|January 8, 2008
Interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-alpha) levels and IL-6, TNF-polymorphisms in children with thrombosisSelma Unal, Fatma Gumruk, Selin Aytac, et al.
Cardiology in the Young|April 17, 2018
Relationship between mean platelet volume-to-lymphocyte ratio and coronary artery abnormalities in Kawasaki diseaseGulcin Bozlu, Derya Karpuz, Olgu Hallioglu, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|August 22, 2018
Vitamin D Deficiency and Its Association with Inflammatory Markers, Lipid Profile and Regulatory T-cells in Pediatric Sickle Cell Disease PatientsYesim Oztas, Selma Unal, Gulcin Eskandari, et al.
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