| Intensive chemotherapy perturbs heart rate variability in children with cancer P Cakan, S Yildiz, A Akyay, Y Öncül Neurophysiologie Clinique 52 (1), 69-80, 2022 | 4 | 2022 |
| Results of multicenter registry for patients with inherited factor VII deficiency in Turkey A Akdeniz, A Ünüvar, MC Ar, E Pekpak, A Akyay, Ö Mehtap, FK Karadağ, ... Scandinavian journal of clinical and laboratory investigation 82 (1), 28-36, 2022 | 2 | 2022 |
| Erythrocyte transfusion restored heart rate variability in children with thalassemia major P Cakan, S Yildiz, A Akyay, Y Öncül Transfusion and Apheresis Science 60 (4), 103156, 2021 | 2 | 2021 |
| Thromboembolism in Children Y Öncül, A Akyay, Ü Özgen Indian Journal of Pediatrics, 1-6, 2023 | 1 | 2023 |
| Hematopoietic stem cell transplantation activities and HRQOL of refugee or asylum seeker children in Turkey: A multicenter study DG Gokcebay, S Küpeli, O Gürsel, OA Bilir, A Akyay, E Pekpak, ... Pediatric transplantation 26 (8), e14397, 2022 | 1 | 2022 |
| Hematopoietic stem cell transplantation activities and HRQOL of refugee or asylum seeker children in Turkey: A multicenter study D Gurlek Gokcebay, S Küpeli, O Gürsel, O Arman Bilir, A Akyay, E Pekpak, ... Pediatric Transplantation 26 (8), e14397, 2022 | 1 | 2022 |
| COVID‐19 disease in children and adolescents following allogeneic hematopoietic stem cell transplantation: A report from the Turkish pediatric bone marrow transplantation study … C Bozkurt, V Hazar, B Malbora, A Küpesiz, U Aygüneş, T Fışgın, ... Pediatric Transplantation 28 (3), e14758, 2024 | | 2024 |
| COVID-19 disease in children and adolescents following hematopoietic stem cell transplantation: A report from the Turkish Pediatric Bone Marrow Transplantation Study Group C BOZKURT, V Hazar, B Malbora, A Küpesiz, U Aygüneş, T Fısgın, ... Authorea Preprints, 2023 | | 2023 |
| Comment on: Eltrombopag for thrombocytopenia following allogeneic hematopoietic stem cell transplantation in children. A Akyay, Y Öncül Pediatric Blood & Cancer 67 (9), e28304-e28304, 2020 | | 2020 |
| A Novel Mutation in a Patient with Wiskott-Aldrich Syndrome Y Öncül, A Akyay, İ Tekedereli | | 2020 |
