Wissenschaftliche Arbeiten
Prof. Dr. Davut Albayrak
152 Publikationen. Neben jeder Publikation steht die Quelle der Angabe.
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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
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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
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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
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TÜRKİYE’DEKİ NADİR KALITSAL HEMOLİTİK ANEMİLERİN FENOTİP- GENOTİP DEĞERLENDİRMESİ
Erciyes University - AVESIS, 2025
Quelle: OpenAlex
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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
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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
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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
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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
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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
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Inhibitor development in mild haemophilia A: Four patients
Haemophilia, 2024
Quelle: ORCID
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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
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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
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Molecular and cytogenetic evaluation of pediatric leukemias
Interdisciplinary Medical Journal, 2024
DOI 10.17944/interdiscip.1596058 Frei zugänglicher VolltextQuelle: OpenAlex
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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
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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
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OUR FAMILIAL MULTIPLE COAGULATION FACTOR DEFICIENCIES CASES
Haemophilia, 2023
Quelle: ORCID
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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CHILDHOOD IMMUNE THROMBOCYTOPENIA: A MULTICENTER QUESTIONNAIRE STUDY
Kocaeli Üniversitesi - AVESİS, 2021
Quelle: OpenAlex
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ESSENTIAL THROMBOCYTOSIS IN CHILDREN
Hematology Transfusion and Cell Therapy, 2021
DOI 10.1016/j.htct.2021.10.1073 Frei zugänglicher VolltextQuelle: OpenAlex
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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
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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
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Eight patients with MYH9-Related Disorder: One Center Results
Haemophilia, 2020
Quelle: ORCID
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FACTOR XII DEFICIENCY: 390 CASES
Haemophilia, 2020
Quelle: ORCID
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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
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TURKEY CONGENITAL THROMBOTIC THROMBOCYTOPENIC PURPURA REGISTRATION SYSTEM RESULTS
Haemophilia, 2020
Quelle: ORCID
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VON WILLEBRAND DISEASE TYPE 3 AND TYPE 1 GENOTYPE RESULTS IN NORTHERN REGION OF TURKEY
Haemophilia, 2020
Quelle: ORCID
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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
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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
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Otoimmun Hemolitik Anemi ve Evans Sendromlu Çocuk Hastalarda Klinik Özelliklerin Değerlendirilmesi
DergiPark (Istanbul University), 2020
Frei zugänglicher VolltextQuelle: OpenAlex
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Çocuklarda Kök Hücre Nakli: Kronik Miyeloid Lösemi
2020
Quelle: OpenAlex
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Glanzmann Trombastenili Hastalarda Lökositlerdeki β2 İntegrin Ekspresyon Düzeylerinin Akım Sitometri ile Ölçülmesi
Kocaeli Üniversitesi - AVESİS, 2020
Quelle: OpenAlex
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Hemofili B Moleküler Analizinde Türkiye Deneyimi: F9 Gen Mutasyon Spektrumu ve Genotip-Fenotip İlişkisi
Bursa Uludag University - AVESIS, 2020
Frei zugänglicher VolltextQuelle: OpenAlex
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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
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Haemophilia A genotype-phenotype analysis in Turkey
Haemophilia, 2019
Quelle: ORCID
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Recombinant factor VIII half life using a bayesian model in patients with severe haemophilia A on prophylaxis in Turkey
Haemophilia, 2019
Quelle: ORCID
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Çok Merkezli Diamond-Blackfan Anemisi Moleküler İnceleme Sonuçları: Eurodba Türkiye
Bursa Uludag University - AVESIS, 2019
Quelle: OpenAlex
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PB2378 ALLOGENEIC STEM CELL TRANSPLANTATION EXPERIENCE IN JUVENILE MYELOMONOCYTIC LEUKEMIA
HemaSphere, 2019
DOI 10.1097/01.hs9.0000567976.99153.49 Frei zugänglicher VolltextQuelle: OpenAlex
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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
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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
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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
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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