Prof. Veysel Sabri Hançer

Articles

• Kruppel-Like Transcription Factor-4 Gene Expression and DNA Methylation Status in Type 2 Diabetes and Diabetic Nephropathy Patients , 2019
• Prevalence of human papilloma virus types in Turkish and Albanian women , 2018
• A Novel Ganciclovir Resistance Mutation in the UL97 Gene of the HHV-5 in an Adult Hematopoietic Stem Cell Transplant Recipient , 2017
• Prognostic significance of carbonic anhydrase IX overexpression in stage III non-small cell lung cancer patients after neoadjuvant treatment , 2018
• Novel Pathological Mutation (c.870 GA, p.Trp290stop) in ARSB of Mucopolysaccharidosis Type VI Patients , 2019
• Case report of a young patient with transthyretin amyloidosis associated with Gly67Ala mutation , 2019
• Evaluation of Tissue Factor -603 A/G Promoter Gene Polymorphism in Thrombotic Processes in Patients with Antiphospholipid Syndrome , 2019
• A novel ATP6V0A2 mutation causing recessive cutis laxa with unusual manifestations of bleeding diathesis and defective wound healing , 2018
• Prophylactic Eculizumab Use in Kidney Transplantation A Review of the Literature and Report of a Case with Atypical Hemolytic Uremic Syndrome , 2015
• P-selectin glycoprotein ligand-1 variable number of tandem repeats polymorphism in young myocardial infarction patients , 2016
• Pharmacogenetic Aspect of Intravitreal Ranibizumab Treatment in Neovascular Age-Related Macular Degeneration: A Five-Year Follow-Up , 2017
• β globin mutations in Turkish, Northern Iraqi and Albanian patients with β thalassemia major , 2018
• Three Factor 11 mutations associated with Factor XI deficiency in a Turkish family , 2018
• Glycoprotein Ibα Kozak polymorphism in patients presenting with early-onset acute coronary syndrome. , 2016
• Renal outcome with eculizumab in two diarrhea-associated haemolytic-uremic syndrome cases with severe neurologic involvement. , 2014
• Three Novel Calreticulin Mutations in Two Turkish Patients , 2017
• Dual effects of testosterone in Behcet s disease implications for a role in disease pathogenesis , 2016
• Non invasive prenatal diagnosis of fetal RhD by using free fetal DNA , 2015
• The Relationship between P Selectin Polymorphisms and Thrombosis in Antiphospholipid Syndrome A Pilot Case Control Study , 2014
• MPL W515L K mutations in chronic myeloproliferative neoplasms , 2013
• Coronary artery ectasia is associated with the c 894G T Glu298Asp polymorphism of the endothelial nitric oxide synthase gene , 2014
• Neurologic involvement in atypical hemolytic uremic syndrome and successful treatment with eculizumab , 2013
• Eculizumab therapy in a child with hemolytic uremic syndrome and CFI mutation , 2012
• The clinical significance of JAK2V617F mutation for Philadelphia negative chronic myeloproliferative neoplasms in patients with splanchnic vein thrombosis , 2012
• Glycoprotein Ib alpha Kozak polymorphism in ischemic stroke , 2012
• The impact of platelet membrane glycoprotein Ib alpha and Ia IIa polymorphisms on the risk of thrombosis in the antiphospholipid syndrome , 2012
• Chronic lymphocytic leukemia developing in a patient with Janus kinase 2 V617F mutation positive myeloproliferative neoplasm , 2012
• ADAMTS 13 gene expression in antiphospholipid syndrome , 2011
• Comparison of KRAS Mutation Tests in Colorectal Cancer Patients , 2011
• Polymorphisms of the angiotensin converting enzyme and angiotensinogen gene in patients with atrial fibrillation , 2011
• Overexpression of Fc Mu Receptor FCMR TOSO Gene In Chronic Lymphocytic Leukemia Patients , 2012
• Activation induced cytidine deaminase mRNA levels in chronic lymphocytic leukemia , 2011
• Cytotoxic T Lymphocyte Antigen 4 CTLA 4 A49G Polymorphism and Autoimmune Blood Diseases , 2010
• Impact of genetic polymorphisms on platelet function and aspirin resistance , 2010
• The prevalence and clinical significance of inherited thrombophilic risk factors in patients with antiphospholipid syndrome , 2010
• Angiotensin converting enzyme gene polymorphism in arrhythmogenic right ventricular dysplasia is DD genotype helpful in predicting syncope risk , 2008
• The association of P selectin glycoprotein ligand 1 VNTR polymorphisms with coronary stent restenosis , 2007
• The association between factor XIII Val34Leu polymorphism and early myocardial infarction , 2006
• Turkish population data on the factor XIII Val34Leu glycoprotein GP Ib Kozak and P selectin glycoprotein ligand 1 PSGL 1 loci , 2005
• Factor XIII Val34Leu polymorphism does not contribute to the prevention of trombotic complication in patients with antiphospholipid syndrome , 2004