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List of works by Veysel Sabri Hancer

A Novel Mutation Causing Recessive Cutis Laxa with Unusual Manifestations of Bleeding Diathesis and Defective Wound Healing

scientific article published on 26 November 2018

ADAMTS-13 gene expression in antiphospholipid syndrome

scientific article

Aberrant Activation-Induced Cytidine Deaminase Gene Expression Links BCR/ABL1-Negative Classical Myeloproliferative Neoplasms

scientific article published in 2022

Activation-induced cytidine deaminase mRNA levels in chronic lymphocytic leukemia ⬇️

scientific article published on December 6, 2010

Chronic lymphocytic leukemia developing in a patient with Janus kinase 2 V617F mutation positive myeloproliferative neoplasm

scientific article published on 17 May 2011

Comparison of KRAS mutation tests in colorectal cancer patients.

scientific article published on 23 June 2011

Cytotoxic T lymphocyte antigen-4 (CTLA-4) A49G polymorphism and autoimmune blood diseases.

scientific article

Dual effects of testosterone in Behcet's disease: implications for a role in disease pathogenesis

scientific article published on 28 July 2016

Eculizumab therapy in a child with hemolytic uremic syndrome and CFI mutation

scientific article

Factor XIII Val34Leu polymorphism does not contribute to the prevention of thrombotic complications in patients with antiphospholipid syndrome.

scientific article

Glycoprotein Ib-alpha Kozak polymorphism in ischemic stroke ⬇️

scientific article published on January 1, 2012

Glycoprotein Ibα Kozak polymorphism in patients presenting with early-onset acute coronary syndrome

scientific article published on 26 October 2016

MPL W515L/K Mutations in Chronic Myeloproliferative Neoplasms

scientific article published on 05 March 2013

Neurologic involvement in atypical hemolytic uremic syndrome and successful treatment with eculizumab.

scientific article

Pharmacogenetic Aspect of Intravitreal Ranibizumab Treatment in Neovascular Age-Related Macular Degeneration: A Five-Year Follow-Up

scientific article published on 04 May 2017

Polymorphisms of the angiotensin-converting enzyme and angiotensinogen gene in patients with atrial fibrillation

scientific article published on 24 March 2011

Prevalence of Human Papilloma Virus Types in Turkish and Albanian Women

scientific article published on 01 October 2018

Prognostic significance of carbonic anhydrase IX overexpression in stage III non-small cell lung cancer patients after neoadjuvant treatment

scientific article published on 11 July 2018

The Relationship between P-Selectin Polymorphisms and Thrombosis in Antiphospholipid Syndrome: A Pilot Case-Control Study.

scientific article published on December 2014

The clinical significance of JAK2V617F mutation for Philadelphia-negative chronic myeloproliferative neoplasms in patients with splanchnic vein thrombosis.

scientific article

The impact of platelet membrane glycoprotein Ib alpha and Ia/IIa polymorphisms on the risk of thrombosis in the antiphospholipid syndrome.

scientific article published on 28 October 2011

The prevalence and clinical significance of inherited thrombophilic risk factors in patients with antiphospholipid syndrome.

scientific article published on April 2010

Three Factor 11 Mutations Associated with Factor XI Deficiency in a Turkish Family.

scientific article

Three Novel Calreticulin Mutations in Two Turkish Patients.

scientific article published on 27 July 2017

Turkish population data on the factor XIII Val34Leu,glycoprotein (GP)Ibalpha Kozak and P-selectin glycoprotein ligand 1 (PSGL-1) loci.

scientific article published in January 2005

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