Prof. Dr. Davut Albayrak
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Person ↔ Disease
Which diseases does this doctor work on?
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Purpura, Thrombocytopenic, Idiopathic 5 publicationsSource: OpenAlex / PubMed MeSHView publications
- Osteopetrosis 4 publications
- Leukemia, Myeloid, Acute 4 publications
- Neutropenia 3 publications
- Leukemia 3 publications
- Nephrotic Syndrome 3 publications
- Anemia, Aplastic 2 publications
- Severe Combined Immunodeficiency 2 publications
- beta-Thalassemia 2 publications
- Thrombasthenia 2 publications
- Fanconi Anemia 2 publications
- Bone Marrow Diseases 2 publications
- Hemorrhagic Fever, Crimean 2 publications
- Thrombocytopenia 2 publications
- Fever 2 publications
- Pleural Effusion 2 publications
- Lymphoma, Non-Hodgkin 2 publications
- Alveolar Bone Loss 2 publications
- Periodontitis 2 publications
Person ↔ Disease
Which topics does this doctor work on?
Medical areas of interest stated by the doctor on the institution profile. Source: medicalpark.com.tr.
- Paediatrics
- Bone marrow transplantation
- Stem cell therapy
- Leukaemia
- Childhood cancer
CV
Education and experience
Experience
- ExperienceMedical Park Samsunmedicalpark.com.tr
Education
- Educationİstanbul University Cerrahpaşa Faculty of Medicine - Medical degreemedicalpark.com.tr
- EducationOndokuz Mayıs University Faculty of Medicine, Paediatrics - Specialty trainingmedicalpark.com.tr
- EducationHacettepe University Faculty of Medicine, Paediatric Haematology - Subspecialty training (fellowship)medicalpark.com.tr
Trust
Where does this information come from?
The source is stated next to each piece of information. If you see something wrong, you can suggest a correction.
- SpecialtyPaediatric Haematology and Oncologymedicalpark.com.trFrom source
- InstitutionMedical Park Samsunmedicalpark.com.trFrom source
- Area of workPurpura, Thrombocytopenic, IdiopathicExtracted from 5 publications · Model version —From source
- Publications152 publicationsOpenAlex, ORCIDFrom source
- ORCID0000-0002-7947-3817ORCIDFrom source
- Last synchronised4 November 2026 20:26https://www.medicalpark.com.tr/hekimler/davut-albayrakmedicalpark.com.tr
Scientific work
Publications on Purpura, Thrombocytopenic, Idiopathic
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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 Open-access full textSource: 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 citations (Europe PMC) Open-access full textSource: 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 citation (Europe PMC) Open-access full textSource: OpenAlex
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TÜRKİYE’DEKİ NADİR KALITSAL HEMOLİTİK ANEMİLERİN FENOTİP- GENOTİP DEĞERLENDİRMESİ
Erciyes University - AVESIS, 2025
Source: 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 Source: 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 Open-access full textSource: 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 Open-access full textSource: 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 citations (Europe PMC) Open-access full textSource: 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 Source: ORCID
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Inhibitor development in mild haemophilia A: Four patients
Haemophilia, 2024
Source: ORCID