Showing results 15 to 34 of 42
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| Issue Date | Title | Author(s) |
| 2011 | Factor V Leiden and Natural Selection | Akar, Mehmet Nejat |
| 2012 | Factor V leiden and prothrombin 20210A mutations among turkish pediatric leukemia patients | Akın, Dilara Fatma; Sipahi, Kadir; Kayaalp, Tugba; Eğin, Yonca; Tasdelen, Serpil; Kurekci, Emin; Akar, Mehmet Nejat |
| 10-May-2018 | A finely resolved phylogeny of Y chromosome Hg J illuminates the processes of Phoenician and Greek colonizations in the Mediterranean | Finocchio, Andrea ; Trombetta, Beniamino ; Messina, Francesco ; D'Atanasio, Eugenia; Akar, Mehmet Nejat ; Loutradis, Aphrodite; Michalodimitrakis, Emmanuel I.; Cruciani, Fulvio ; Novelletto, Andrea |
| 2014 | FIRST OBSERVATION OF DE NOVO MYH9 GENE MUTATION IN A PATIENT WITH MACROTHROMBOCYTOPENIA | Torun, Didem; Duman, T.; Akar, Mehmet Nejat |
| 2016 | FIRST OBSERVATION OF TUBB1 GENE MUTATIONS IN TURKISH PATIENTS WITH MACROTHROMBOCYTOPENIA | Özkan, D. T.; Waheed, A. A.; Kandilci, A.; Akar, Mehmet Nejat |
| 2018 | Frequency of thiopurine S-methyltransferase gene variations in Turkish children with acute leukemia | Akın, Dilara Fatma; Aşlar-Öner, Deniz; Kürekçi, Emin; Akar, Mehmet Nejat |
| Sep-2018 | Frequency of vitamin K oxidoreductase complex subunit-1 (VKORC1) polymorphisms and warfarin dose management in patients with venous thromboembolism | Kabalak, Pınar Akın; Savaş, İsmail; Akar, Mehmet Nejat ; Demir, Nalan; Eğin, Yonca |
| Sep-2020 | Further note on Hemoglobin Fontainebleau (a21(B2) Ala-Pro) | Akar, Mehmet Nejat ; Ardıçoğlu Akışın, Nazife Yasemin |
| 2013 | High resolution transcriptomic analysis of trousseau syndrome | Dalkılıç, S.; Özkeserli, Z.; İlk, O.; Oğuzülgen, I. K.; Akar, Mehmet Nejat ; Özdağ, H. |
| Jan-2019 | A Human Mission: Dumlupinar | Akar, Mehmet Nejat |
| 2011 | Kikuchi-fujimoto disease associated with aseptic meningitis: A case report | Arslan Z. ; Uysal O.; Özön A.; Rad A.; Atacanli A.; Akar, Mehmet Nejat ; Sümer M. |
| 2014 | NOVEL MUTATIONS AT GPIIB/GPIIIA GENES FROM TURKISH PATIENTS WITH GLANZMANN THROMBASTHENIA SYNDROME | Özkan, D. T.; Çalışkan, U.; Akar, Mehmet Nejat |
| Jul-2018 | A novel MYH9 mutation in a beta thalassemia major patient with thrombocytopenia. | Özkan, Didem Torun; Akar, Mehmet Nejat |
| 2016 | Novel TUBB1 gene mutations in Turkish patients with macrothrombocytopenia | Özkan, D. T.; Waheed, A. A.; Kandilci, A.; Akar, Mehmet Nejat |
| 2020 | Platelet Satellitism | Ardıçoğlu Akışın, Nazife Yasemin ; Akar, Mehmet Nejat |
| 2015 | Radioactive fallout and neural tube defects | Akar, Nejat |
| 2012 | The role of factor v leiden in adult patients with venous thromboembolism: A meta-analysis of published studies from Turkey | Eroğlu, A.; Sertkaya, D.; Akar, Mehmet Nejat |
| 2016 | The Role Of Platelet-To-Lymphocyte Ratio In The Diagnosis Of Infectious Mononucleosis [Conference Object] | Karagöz, Z. N.; Akışın, Y. A.; Turan, M.; Akar, Mehmet Nejat |
| 2015 | SCREENING FOR VARIATIONS IN EXONS 9, 10 AND 12 OF CD22 GENE IN CHILDHOOD ACUTE LYMPHOBLASTIC LEUKEMIA | Aslar, D.; Akın, D. F.; Mumcuoğlu, M.; Ezer, U.; Kürekci, E.; Akar, Mehmet Nejat |
| 2016 | SCREENING OF EPCR VARIANTS AND THEIR CORRELATION WITH FACTOR V LEIDEN AND PROTHROMBIN 20210A MUTATIONS IN TURKISH PEDIATRIC PATIENTS WITH ACUTE LEUKEMIA | Akın, D. F.; Öner, D. A.; Sipahi, K.; Mumcuoğlu, M.; Kürekci, E.; Ezer, U.; Akar, Mehmet Nejat |
