Browsing by Author "Özdilli, Kürşat"
Now showing items 1-20 of 34
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Association study of CFH Y402H functional variant with genetic susceptibility to nicotine dependence and schizophrenia in Turkish population
Sever, Ülgen; Nursal, Ayşe Feyda; Çetinay Aydın, Pınar; Uysal, Mehmet Ali; Özdilli, Kürşat; Pehlivan, Mustafa; Aydın, Nur Gökçe; Pehlivan, Sacide (American Society for Cell Biology, 2018)... -
Chronic neutropenia in childhood: Laboratory and clinical features
Nepesov, Serdar; Yaman, Yöntem; Elli, Murat; Bayram, Nihan; Özdilli, Kürşat; Ayaz, Akif; Anak, Sema (Springer India, 2022)Objectives To describe the clinical characteristics of patients with chronic neutropenia. Methods Data of 36 patients with chronic neutropenia, who were followed up in the authors' clinic between May 2013 and May 2020, ... -
Clinical efficacy of ruxolitinib monotherapy and haploidentical hematopoeitic stem cell transplantation in a child with philadelphia chromosome-like relapsed/refractory acute lymphoblastic leukemia
Bayram, Nihan; Yaman, Yöntem; Özdilli, Kürşat; Telhan, Leyla; Nepesov, Serdar; Bilgen, Hülya; Elli, Murat; Behar, Sude Sema; Anak, Sema (Wiley, 2021)Introduction (Ph-like) ALL is a subset of leukemia which has a gene expression profile similar to Ph+disease, but without the presence of BCR-ABL1 translocation. Case description We reported an exceptional case of a ... -
Clinical, genetic, and outcome characteristics of pediatric patients with primary hemophagocytic lymphohistiocytosis
Nepesov, Serdar; Yaman, Yöntem; Elli, Murat; Bayram, Nihan; Özdilli, Kürşat; Kıykım, Ayça; Çakır, Deniz; Kılıç, Betül; Aydın, Kürşad; Ayaz, Akif; Telhan, Leyla; Anak, Sema (AVES, 2022)Objectİive: In this study, we sought to describe the clinical, laboratory, and genetic characteristics of patients diagnosed with primary hemophagocytic lymphohistiocytosis. Thus, we aimed to evaluate the early diagnosis ... -
Cytokine gene polymorphism frequencies in Turkish population living in Marmara region
Özdilli, Kürşat; Duvarcı Öğret, Yeliz; Oğuz, Süleyman Rüştü; Abatay Sel, Figen; Şentürk Çiftçi, Hayriye; Kekik Çınar, Çiğdem; Pehlivan, Sacide; Savran Oğuz, Fatma (De Gruyter Open Ltd, 2022)Objectives Sequence variants in cytokine genes are related to affect cytokine gene levels. In this study, it was aimed to examine eight single nucleotide polymorphisms (SNPs) in five cytokine genes (TNF-alpha, INF-gamma, ... -
Determination of burnout and job satisfaction levels in nurses working in the surgical clinics
Objective: The aim of this study was to assess the effect of sociodemographic and professional characteristics of nurses working in thesurgical services on their burnout and job satisfaction levels.Method: The study was ... -
DNA repair genes and chronic myeloid leukemia: ERCC2 (751), XRCC1 (399), XRCC4-Intron 3, XRCC4 (-1394) gene polymorphisms
Özdilli, Kürşat; Pehlivan, Mustafa; Serin, İstemi; Oğuz Savran, Fatma; Tomatır, Ayşe Gaye; Pehlivan, Sacide (Mattioli 1885, 2021)To the editor. Chronic myeloid leukemia (CML), which is characterized by the overproduction of mature cells in the granulocytic series, is included in the group of chronic myeloproliferative neoplasms.1 It is the first ... -
Do UCP2, IL-17, mi196a2, and NR3C1 gene variants contribute to the risk of microtia? A preliminary study in Turkish population
Özdilli, Kürşat; Bekerecioğlu, Mehmet; Nursal, Ayşe Feyda; Pehlivan, Mustafa; Sever, Ülgen; Büyükgüral, Berker; Pehlivan, Sacide (Elsevier Science Bv, 2018)Microtia is a congenital malformation of variable severity of theexternal and middle ear. Although many genetic and environmen-tal factors are investigated the etiopathogenesis of microtia, it isstill uncertain. We performed ... -
Effect of cytokine genes in the pathogenesis and on the clinical parameters for the treatment of multiple myeloma
Haydaroğlu, Handan; Oğuzkan Balcı, Sibel; Pehlivan, Sacide; Özdilli, Kürşat; Gündoğan, Ersin; Okan, Vahap; Nursal, Ayşe Feyda; Pehlivan, Mustafa (Taylor & Franis Ltd, 2017)In this study, we aimed to explore the association among gene variants of five cytokines, tumor necrosis factor alpha (TNF-alpha), transforming growth factor beta-1 (TGF-beta 1), interferon gamma (IFN-gamma), interleukin-6 ... -
Eltrombopag for treatment of thrombocytopenia after allogeneic hematopoietic cell transplantation in children: Single-centre experience
Yaman, Yöntem; Elli, Murat; Şahin, Şifa; Özdilli, Kürşat; Bilgen, Hülya; Bayram, Nihan; Nepesov, Serdar; Anak, Sema (Wiley, 2021)Delayed recovery of thrombocytopenia is a well-known complication after allogeneic HSCT. Eltrombopag (ELT), a thrombopoietin receptor agonist (TRAs), induces platelet maturation and release. Mostly conducted in adults, ... -
Eltrombopag use for post hematopoetic stem cell transplantation thrombocytopenia in pediatric patients
Elli, Murat; Yaman, Yöntem; Özdilli, Kürşat; Bilgen, Hülya; Çakır, Aslı; Şahin, Şifa; Anak, Sema (Nature Publishing Group, 2019)... -
Gene polymorphisms and febrile neutropenia in acute leukemia-no association with IL-4, CCR-5, IL-1RA, but the MBL-2, ACE, and TLR-4 are associated with the disease in Turkish patients: A preliminary study
Pehlivan, Mustafa; Haydaroğlu Şahin, Handan; Özdilli, Kürşat; Onay, Hüseyin; Özcan, Ali; Özkinay, Ferda; Pehlivan, Sacide (Mary Ann Liebert, Inc., 2014)Aims: The aim of this study was to investigate the mannose-binding lectin 2 (MBL-2), interleukin (IL)-4, Toll-like receptor 4 (TLR-4), angiotensin converting enzyme (ACE), chemokine receptor 5 (CCR-5), and IL-1 receptor ... -
Genetic polymorphisms in 15 STR loci in the Turkish population living in İstanbul province
Özdilli, Kürşat; Duvarcı Öğret, Yeliz; Oğuz, Rüştü; İşsever, Halim; Yokeş, Mehmet Baki; Şentürk Çiftci, Hayriye; Abatay Sel, Figen; Kıvanç, Demet; Kekik Çınar, Çiğdem; Pehlivan, Sacide; Savran Oğuz, Fatma (Nobelmedicus, 2022)Objective: Short tandem repeats (STRs) are short sequences of nucleotides that are repeated and distributed all over the genome. These polymorphisms enable investigation of the forensic, ancestral lineage and evolutionary ... -
Graft-versus-host disease in a child with neuroblastoma after autologous stem cell transplantation
Yaman, Yöntem; Baysoy, Gökhan; Keleşoğlu, Emre; Özdilli, Kürşat; Çakır, Aslı; Genç, Dildar Bahar; Elli, Murat; Anak, Sema (Termedia Publishing House Ltd, 2019)In the pediatric population, hematopoietic stem cell transplantation (HSCT) is used to treat a wide variety of diseases, both malignant and nonmalignant. For many of these diseases, HSCT is a well-established treatment. ... -
Hematopoietic stem cell transplantation in patients with severe combined immunodeficiency: A single-center experience
Nepesov, Serdar; Yaman, Yöntem; Elli, Murat; Bayram, Nihan; Özdilli, Kürşat; Kıykım, Ayça; Anak, Sema (Istanbul University, 2022)Objective: The aim of this study was to determine the factors affecting outcomes in patients who underwent hematopoietic stem cell transplantation (HSCT) with the diagnosis of severe combined immunodeficiency (SCID). ... -
High ferritin levels in fever of unknown origin: Possible first sign of hemophagocytosis in bmt patients?
Yaman, Yeşim; Hazar, Volkan; Sarıbeyoğlu, Ebru; Özdilli, Kürşat; Anak, Sema (Ferrata Storti Foundation, 2016)... -
High soluble CD30 levels and associated anti-HLA antibodies in patients with failed renal allografts
Karahan, Gonca Emel; Çalışkan, Yaşar; Özdilli, Kürşat; Kekik, Çiğdem; Bakkaloğlu, Hüseyin; Çalışkan, Bahar; Türkmen, Aydın; Sever, Mehmet Şükrü; Savran Oǧuz, Fatma (Sage Publications Ltd., 2016)Introduction: Serum soluble CD30 (sCD30), a 120-kD glycoprotein that belongs to the tumor necrosis factor receptor family, has been suggested as a marker of rejection in kidney transplant patients. The aim of this study ... -
HLA - matched related donor hematopoietic stem cell transplantation in a patient with polynucleotide kinase 3-phosphatase mutation developed acute myeloid leukemia
Bayram, Nihan; Yaman, Yöntem; Elli, Murat; Özdilli, Kürşat; Nepesov, Serdar; Doğan, Mehmet Sait; Ayaz, Akif; Anak, Sema (Wiley, 2022)Background PNPK gene mutations result in DNA repair disorders and have a spectrum of neurodevelopmental manifestations. To date, cancer predisposition has not been described in patients with PNKP mutations. Observation ...
