Wissenschaftliche Arbeiten

Prof. Dr. Davut Albayrak

152 Publikationen. Neben jeder Publikation steht die Quelle der Angabe.

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  1. Frequency, Characteristics, Management, and Outcomes of Posttransplant Lymphoproliferative Disorder After Allogeneic Hematopoietic Stem Cell Transplantation in Children: A Multicentre Retrospective Study of the Turkish Pediatric BMT Study Group

    Turkish Journal of Hematology, 2026

    DOI 10.4274/tjh.galenos.2026.55376 PMID 41778738 Frei zugänglicher VolltextQuelle: OpenAlex

  2. A Multicenter, Retrospective Study Comparing Immunosuppressive Therapy Combined with Eltrombopag to Immunosuppressive Therapy Alone as Front-Line Treatment for Pediatric Severe Aplastic Anemia

    Turkish Journal of Hematology, 2025

    DOI 10.4274/tjh.galenos.2025.2025.0245 PMID 40788204 2 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  3. Genetic heterogeneity in childhood leukemia/lymphoma: a Turkish cohort with strong predisposition

    Frontiers in Genetics, 2025

    DOI 10.3389/fgene.2025.1624306 PMID 40995433 1 Zitation (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  4. TÜRKİYE’DEKİ NADİR KALITSAL HEMOLİTİK ANEMİLERİN FENOTİP- GENOTİP DEĞERLENDİRMESİ

    Erciyes University - AVESIS, 2025

    Quelle: OpenAlex

  5. Case Report: Coexistence of Giant Congenital Melanocytic Nevus and Holocord Spinal Nerve Sheath Tumor

    Fetal and Pediatric Pathology, 2025

    DOI 10.1080/15513815.2025.2585053 PMID 41259004 Quelle: ORCID

  6. Genetic and clinical characterization of factor VII deficiency: insights from 34 Turkish patients

    Blood Coagulation & Fibrinolysis, 2025

    DOI 10.1097/mbc.0000000000001381 PMID 40748016 Frei zugänglicher VolltextQuelle: OpenAlex

  7. COVID‐19 disease in children and adolescents following allogeneic hematopoietic stem cell transplantation: A report from the Turkish pediatric bone marrow transplantation study group

    Pediatric Transplantation, 2024

    DOI 10.1111/petr.14758 PMID 38659218 Frei zugänglicher VolltextQuelle: OpenAlex

  8. Identification of the molecular etiology in rare congenital hemolytic anemias using next‐generation sequencing with exome‐based copy number variant analysis

    European Journal Of Haematology, 2024

    DOI 10.1111/ejh.14194 PMID 38556258 3 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  9. Clinical features and risk factors of hepatic sinusoidal obstruction syndrome in children after hematopoietic stem cell transplantation: A single-center experience

    Transfusion and Apheresis Science, 2024

    DOI 10.1016/j.transci.2024.103909 PMID 38467529 Quelle: ORCID

  10. Inhibitor development in mild haemophilia A: Four patients

    Haemophilia, 2024

    Quelle: ORCID

  11. Retrospective analysis of hemophilia B in Turkey: identifying main characteristics and treatment options

    Research and Practice in Thrombosis and Haemostasis, 2024

    DOI 10.1016/j.rpth.2024.102588 PMID 39582809 Frei zugänglicher VolltextQuelle: ORCID

  12. Risk factors for neurologic sequelae in children and adolescents with hemophilia after intracranial hemorrhage

    Research and Practice in Thrombosis and Haemostasis, 2024

    DOI 10.1016/j.rpth.2024.102607 PMID 39687930 3 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  13. Molecular and cytogenetic evaluation of pediatric leukemias

    Interdisciplinary Medical Journal, 2024

    DOI 10.17944/interdiscip.1596058 Frei zugänglicher VolltextQuelle: OpenAlex

  14. PB2401: DETERMINING MOLECULAR BACKGROUND OF A GROUP OF CHILDHOOD LEUKEMIA/LYMPHOMA PATIENTS WITH POSITIVE FAMILY HISTORY FROM TÜRKIYE

    HemaSphere, 2023

    DOI 10.1097/01.hs9.0000976316.59261.07 Frei zugänglicher VolltextQuelle: OpenAlex

  15. Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients

    Clinical Immunology, 2023

    DOI 10.1016/j.clim.2023.109757 PMID 37689091 10 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  16. OUR FAMILIAL MULTIPLE COAGULATION FACTOR DEFICIENCIES CASES

    Haemophilia, 2023

    Quelle: ORCID

  17. Thalassemia-free and graft-versus-host-free survival: outcomes of hematopoietic stem cell transplantation for thalassemia major, Turkish experience

    Bone Marrow Transplantation, 2022

    DOI 10.1038/s41409-022-01613-w PMID 35210564 20 Zitationen (Europe PMC) Quelle: OpenAlex

  18. A Significant Association in Paediatric Emergency Department, Cerebral Sinovenous Thrombosis and Ulcerative Colitis: Review of Literature

    West Indian Medical Journal, 2022

    DOI 10.7727/wimj.2015.290 Frei zugänglicher VolltextQuelle: ORCID

  19. New αIIbβ3 variants in 28 Turkish Glanzmann patients; structural hypothesis for complex activation by residues variations in I-EGF domains

    Platelets, 2022

    DOI 10.1080/09537104.2021.1947481 PMID 34275420 4 Zitationen (Europe PMC) Quelle: ORCID

  20. Acute severe headache: Association of herpes zoster meningitis and sinus vein thrombosis

    Journal of Surgery and Medicine, 2022

    DOI 10.28982/josam.978248 Frei zugänglicher VolltextQuelle: OpenAlex

  21. Different Kinetics and Risk Factors for Isolated Extramedullary Relapse after Allogeneic Hematopoietic Stem Cell Transplantation in Children with Acute Leukemia

    Transplantation and Cellular Therapy, 2021

    DOI 10.1016/j.jtct.2021.06.023 PMID 34216791 6 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  22. CHILDHOOD IMMUNE THROMBOCYTOPENIA: A MULTICENTER QUESTIONNAIRE STUDY

    Hematology Transfusion and Cell Therapy, 2021

    DOI 10.1016/j.htct.2021.10.1070 Frei zugänglicher VolltextQuelle: OpenAlex

  23. Flow cytometric analysis of platelet surface glycoproteins in the diagnosis of thirty-two turkish patients with glanzmann thrombasthenia: A multicenter experience

    Turkish Journal of Medical Sciences, 2021

    DOI 10.3906/sag-2006-107 PMID 33957723 6 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  24. Clinical follow-up of children with high vitamin B12 values: should we worry?

    Turkish Journal of Pediatrics, 2021

    DOI 10.24953/turkjped.2021.06.015 PMID 35023657 6 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  25. Covid-19 Infection in children with Cancer after the First Wave in Turkey: A Study of the Turkish Pediatric Oncology (TPOG) and Hematology (TPHD) Societies

    Pediatric Blood and Cancer, 2021

    Quelle: ORCID

  26. Neuroprotective Efficacy of Prophylactic Antiepileptic Therapies in Busulfan Conditioning Regimen

    Journal of Pediatric Neurology, 2021

    DOI 10.1055/s-0040-1708833 1 Zitation (OpenAlex) Quelle: ORCID

  27. CHILDHOOD IMMUNE THROMBOCYTOPENIA: A MULTICENTER QUESTIONNAIRE STUDY

    Kocaeli Üniversitesi - AVESİS, 2021

    Quelle: OpenAlex

  28. ESSENTIAL THROMBOCYTOSIS IN CHILDREN

    Hematology Transfusion and Cell Therapy, 2021

    DOI 10.1016/j.htct.2021.10.1073 Frei zugänglicher VolltextQuelle: OpenAlex

  29. Blood Product Requirement in Childhood Acute Myeloid Leukemia by Chemotherapy Regimens

    Turkish Journal of Pediatric Disease, 2020

    DOI 10.12956/tchd.587123 1 Zitation (OpenAlex) Frei zugänglicher VolltextQuelle: ORCID

  30. Blood product requirement in childhood acute lymphoblastic leukemia in relation to chemotherapy regimens

    Iranian Journal of Pediatrics, 2020

    DOI 10.5812/ijp.100823 2 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: ORCID

  31. Eight patients with MYH9-Related Disorder: One Center Results

    Haemophilia, 2020

    Quelle: ORCID

  32. FACTOR XII DEFICIENCY: 390 CASES

    Haemophilia, 2020

    Quelle: ORCID

  33. Spontaneus Triplet Birth After Acute Lymphoblastic Leukemia Treatment

    Indian Journal of Hematology and Blood Transfusion, 2020

    DOI 10.1007/s12288-019-01230-6 PMID 32647435 Frei zugänglicher VolltextQuelle: ORCID

  34. TURKEY CONGENITAL THROMBOTIC THROMBOCYTOPENIC PURPURA REGISTRATION SYSTEM RESULTS

    Haemophilia, 2020

    Quelle: ORCID

  35. VON WILLEBRAND DISEASE TYPE 3 AND TYPE 1 GENOTYPE RESULTS IN NORTHERN REGION OF TURKEY

    Haemophilia, 2020

    Quelle: ORCID

  36. Turkey experience in molecular analysis of hemophilia b: F9 gene mutation spectrum and genotype-phenotype correlation,Hemofili b moleküler analizinde türkiye deneyimi: F9 gen mutasyon spektrumu ve genotip-fenotip ilişkisi

    Turkiye Klinikleri Journal of Medical Sciences, 2020

    DOI 10.5336/medsci.2020-75066 Frei zugänglicher VolltextQuelle: ORCID

  37. Autoimmune hemolytic anemia in children, 20 years experience of single center

    Annals of Medical Research, 2020

    DOI 10.5455/annalsmedres.2019.10.672 1 Zitation (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  38. Otoimmun Hemolitik Anemi ve Evans Sendromlu Çocuk Hastalarda Klinik Özelliklerin Değerlendirilmesi

    DergiPark (Istanbul University), 2020

    Frei zugänglicher VolltextQuelle: OpenAlex

  39. Çocuklarda Kök Hücre Nakli: Kronik Miyeloid Lösemi

    2020

    Quelle: OpenAlex

  40. Glanzmann Trombastenili Hastalarda Lökositlerdeki β2 İntegrin Ekspresyon Düzeylerinin Akım Sitometri ile Ölçülmesi

    Kocaeli Üniversitesi - AVESİS, 2020

    Quelle: OpenAlex

  41. Hemofili B Moleküler Analizinde Türkiye Deneyimi: F9 Gen Mutasyon Spektrumu ve Genotip-Fenotip İlişkisi

    Bursa Uludag University - AVESIS, 2020

    Frei zugänglicher VolltextQuelle: OpenAlex

  42. Does Vitamin B12 Deficiency in Infants Cause Severe Clinical Symptoms Necessitating Intensive Care?

    Turkish Journal of Pediatric Emergency and Intensive Care Medicine, 2019

    DOI 10.4274/cayd.galenos.2019.47568 2 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: ORCID

  43. Haemophilia A genotype-phenotype analysis in Turkey

    Haemophilia, 2019

    Quelle: ORCID

  44. Recombinant factor VIII half life using a bayesian model in patients with severe haemophilia A on prophylaxis in Turkey

    Haemophilia, 2019

    Quelle: ORCID

  45. Çok Merkezli Diamond-Blackfan Anemisi Moleküler İnceleme Sonuçları: Eurodba Türkiye

    Bursa Uludag University - AVESIS, 2019

    Quelle: OpenAlex

  46. PB2378 ALLOGENEIC STEM CELL TRANSPLANTATION EXPERIENCE IN JUVENILE MYELOMONOCYTIC LEUKEMIA

    HemaSphere, 2019

    DOI 10.1097/01.hs9.0000567976.99153.49 Frei zugänglicher VolltextQuelle: OpenAlex

  47. Neonates born to mothers with immune thrombocytopenia: 11 years experience of a single academic center

    Blood Coagulation and Fibrinolysis, 2018

    DOI 10.1097/mbc.0000000000000758 PMID 30036278 10 Zitationen (Europe PMC) Quelle: ORCID

  48. Prevalance of iron deficiency and iron deficiency anemia among 7-14 years old children in Samsun

    Izmir Dr Behcet Uz Cocuk Hastanesi Dergisi, 2018

    DOI 10.5222/buchd.2018.122 3 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: ORCID

  49. Plasma Exchange in Critically Ill Children: A Single-center Experience

    Turkish Journal of Pediatric Emergency and Intensive Care Medicine, 2018

    DOI 10.4274/cayd.28199 4 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  50. Juvenile Myelomonocytic Leukemia in Turkey: A Retrospective Analysis of Sixty-five PatientsÖzlem Tüfekçi1

    Turkish Journal of Hematology, 2017

    DOI 10.4274/tjh.2017.0021 PMID 28179213 9 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex