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Journal of Clinical Apheresis|October 20, 2004
Plasmapheresis in the treatment of hyperthyroidism associated with agranulocytosis: A case reportBirol Guvenc, Cagatay Unsal, Emel Gurkan, et al.Advances in Therapy|October 20, 2006
Clinical significance of hepatocyte growth factor, platelet-derived growth factor-AB, and transforming growth factor-alpha in bone marrow and peripheral blood of patients with multiple myelomaIsmail Oguz Kara, Berksoy Sahin, Ramazan Gunesacar, et al.Journal of the National Medical Association|July 23, 2005
Sickle cell anemia patient with sarcoidosis-associated inguinal lymph node and lung infiltrationBirol Güvenç, Cagatay Unsal, Ismail Hanta, et al.Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|August 6, 2004
Systemic lupus erythematosus and thrombotic thrombocytopenic purpura: a case reportBirol Guvenc, Cagatay Unsal, Emel Gurkan, et al.International Journal of Hematology|September 9, 2005
Renal vascular resistance in sickle cell painful crisisBirol Guvenc, Kairgeldy Aikimbaev, Cagatay Unsal, et al.Hemoglobin|March 6, 2012
Nonsense β-thalassemia mutation at codon 37 (TGG>TGA), detected for the first time in three Turkish casesSevcan Tug Bozdogan, Cagatay Unsal, Hakan Erkman, et al.Archives of Medical Science : AMS|August 2, 2012
β-Thalassemia mutations and hemoglobinopathies in Adana, Turkey: results from a single center studyBirol Guvenc, Abdullah Canataroglu, Cagatay Unsal, et al.Archives of Medical Science : AMS|October 12, 2012
β-Globin chain abnormalities with coexisting α-thalassemia mutationsBirol Guvenc, Abdullah Canataroglu, Cagatay Unsal, et al.Pageof 1