Browsing by Author Akar, Nejat

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Issue DateTitleAuthor(s)
2014Assessment of HbF QTLs Affecting Disease Severity and Genetic Analysis in Patients Homozygous for Codon 8 (-AA) beta(0)-Thalassemia MutationJiang, Zhihua; Huang, Shengwen; Luo, Hong Yuan; Akar, Nejat; Başak, A. Nazlı; Al-Allawi, Nasir; Chui, David H. K.
2019Asymptomatic hemochromatosis case with HFE c.1007−47G>A, c.340+4T>C heterozygous mutations and alpha globin −3.7 kb deletionÇelik, Vesile Deniz; Kılıç, Betül Orhan; Ardıçoğlu Akışın, Nazife Yasemin ; Akar, Nejat
2016Behcet's: A Disease or a Syndrome? Answer from an Expression Profiling StudyOğuz, Ali Kemal; Yılmaz, Seda Tasir; Oygur, Çağdaş Sahap; Candar, Tuba; Sayın, Irmak; Kılıçoğlu, Sibel Serin; Akar, Nejat
2022Beta-lactam antibiotic-induced thrombocytopenia: MYH9 & TUBB1 genesOzkan, Didem; Akisin, Yasemin Ardicoglu; Bali, Dilara Fatma Akin; Akar, Nejat
2015Cerebral Sinovenous Thrombosis in Children and Neonates: Clinical Experience, Laboratory, Treatment, and OutcomeBektaş, Ömer; Teber, Serap; Akar, Nejat; Uysal, Leyla Zümrüt; Arsan, Saadet; Ataşay, Begüm; Deda, Gülhis
2012Comprehensive identification of erythrocyte membrane protein deficiency by 2D gel electrophoresis based proteomic analysis in hereditary elliptocytosis and spherocytosisDemiralp, Duygu Özel; Peker, Selen; Turgut, Burhan; Akar, Nejat
2018Determination of CEBPA mutations by next generation sequencing in pediatric acute leukemiaAkın, DF; Öner, DA; Kürekci, E; Akar, Nejat
2019Diamond-Gardner Syndrome: Autoerythrocyte Sensitization SyndromeAkar, Nejat; Karagöz, Zeynep Nur; Ardıçoğlu Akışın, Nazife Yasemin 
2012Does FVL have an effect on longevity?Akın, Dilara Fatma; Eğin, Yonca; Akar, Nejat
2019Effects of Ankaferd Hemostat on Helicobacter pylori strains and antibiotic resistanceÇiftçiler, R.; Koluman, A.; Haznedaroğlu, İbrahim Celalettin; Akar, Nejat
Sep-2016Endothelial Cells, Ankaferd Hemostat, And EstradiolArdıçoğlu Akışın, Nazife Yasemin ; Akar, Nejat; Haznedaroğlu, İbrahim
2012A further note on filicide with suicide in TurkeyAkar, Nejat
2016A Further Note on the Thalassemia Screening Program in the Mugla Region of TurkeyAkar, Nejat
Jan-2020Further observation of Hemoglobin Fontainebleau (a21(B2) Ala-Pro) in a Turkish familyAkar, Nejat; Ceylaner, Serdar; Ardıçoğlu Akışın, Nazife Yasemin ; Taştan, Gökçe Su
2014gamma A gene repeats polymorphism for the analysis of haplotypes of abnormal hemoglobinsAkar, Nejat; Sipahi, Kadir; Akar, Ece; Yılmaz, Erkan
Dec-2020Genetic Analysis of Afibrinogenemia and Hypofibrinogenemia: Novel Mutations in the FGB Gene in the Turkish PopulationÖzkan, Didem Torun; Sarper, Nazan; Akar, Nejat
2022Genetic Profiling of Pediatric Patients with B-Cell Precursor Acute Lymphoblastic LeukemiaAkin-Bali, Dilara Fatma; Erdogan, Beyza Doganay; Oner, Deniz Aslar; Mahmud, Akkan; Tasdelen, Serpil; Kurekci, Emin; Akar, Nejat
2021Glucose-6-phosphate dehydrogenase gene Ala365Thr mutation in an Iraqi family with confusing clinical differencesArdıçoğlu Akışın, N. Yasemin; Arslan, Zafer ; Ceylaner, Serdar; Akar, Nejat
2016Grandmother's Effect On Child Weight In Turkish CommunityAkar, Nejat
2016Hemoglobin H Disease in Turkey: Experience from Eight CentersÜnal, Selma; Oktay, Gönül; Acıpayam, Can; İlhan, Gül; Gali, Edip; Celkan, Tiraje; Toptaş, Tayfur; Akar, Nejat