Browsing by Author "Buyukdogan, Murat"
Now showing items 1-8 of 8
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Cholangitis, döhle bodies, may-hegglin anomaly
Cholangitis, Döhle bodies, May-Hegglin anomaly -
A novel ganciclovir resistance mutation in the UL97 gene of the HHV-5 in an adult hematopoietic stem cell transplant recipient
Hancer, Veysel Sabri; Saglam Yarimcan, Filiz; Buyukdogan, Murat; Aki, Sahika Zeynep; Oksuz, Burcu; Acar, Kadir; Acar, Muradiye; Bulut, Pelin (Future Medicine Ltd, 2017)Therapeutic management of cytomegalovirus (CMV) disease in hematopoietic stem cell transplantation patients can become a challenge because of the emergence of anti-CMV drug resistance. This case report presents a patient ... -
A novel pathological arsb mutation (c.870G>A; p.Trp290stop) in mucopolysaccharidosis type VI patients
Hancer, Veysel Sabri; Buyukdogan, Murat; Babameto-Laku, Anila (Karger, 2019)Mucopolysaccharidosis (MPS) type VI, also known as Maroteaux-Lamy syndrome, is a lysosomal storage disorder, characterized by the deficiency of the arylsulfatase B enzyme. The clinical phenotype and severity of the illness ... -
Prevalence of human papilloma virus types in Turkish and Albanian women
Hancer, Veysel Sabri; Buyukdogan, Murat; Bylykbashi, Ilta; Oksuz, Burcu; Acar, Muradiye (Wolters Kluwer Medknow Publications, 2018)Background: Human papilloma virus (HPV) infection is the major etiologic agent of cervical carcinoma. The aim of this study was to determine the prevalence of HPV infection and genotype distribution in cervical swabs from ... -
Prognostic significance of carbonic anhydrase IX overexpression in stage III non-small cell lung cancer patients after neoadjuvant treatment
Ibis, Kamuran; Saglam, Sezer; Saglam, Esra Kaytan; Firat, Pinar; Yilmazbayhan, Dilek; Toker, Alper; Ozkan, Berker; Hancer, Veysel Sabri; Buyukdogan, Murat; Disci, Rian; Pilanci, Kezban Nur (Elsevier Gmbh, Urban & Fischer Verlag, 2018)Background: To assess the prognostic importance of carbonic anhydrase IX (CA IX), a hypoxic biomarker, after neoadjuvant treatment in Stage III non-small cell lung cancer (NSCLC) patients. Methods: Tissue CA IX expression ... -
Three factor 11 mutations associated with factor XI deficiency in a Turkish family
Hancer, Veysel Sabri; Gokgoz, Zafer; Buyukdogan, Murat (Galenos Yayincilik, 2018)Factor XI (FXI) is a homodimeric serine protease, which is produced in the liver and circulates in the plasma complexed with high-molecular-weight kininogen. FXI plays an important role in the amplification of the initial ... -
Three novel calreticulin mutations in two Turkish patients
Hancer, Veysel Sabri; Tokgoz, Huseyin; Guvenc, Serkan; Caliskan, Umran; Buyukdogan, Murat (Galenos Yayincilik, 2017)Calreticulin (CALR) mutations were first identified exclusively in JAK2-MPL-negative essential thrombocythemia (ET) and primary myelofibrosis (PMF) at a rate of 60%-88%, accounting for 1/4 to 1/3 of all patients with ... -
Two rare pathogenic HBB variants in a patient with beta-thalassemia intermedia
Hancer, Veysel Sabri; Fisgin, Tunc; Buyukdogan, Murat (Galenos Yayincilik, 2020)The β-thalassemias are a group of hereditary disorders with autosomal recessive inheritance characterized by the presence of defective synthesis of the β-globin chain, an integral component of the hemoglobin molecule, ...
