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Hamza Okur

Hacettepe University

37

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515

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Both Granulocytic and Non-Granulocytic Blood Cells Are Affected in Patients with Severe Congenital Neutropenia and Their Non-Neutropenic Family Members: An Evaluation of Morphology, Function, and Cell Death

2018 Turkish Journal of Hematology
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P3.03-052 Diagnostic Utility of Mesothelin, Osteopontin and Megakaryocyte Potentiation Factor in Turkish Patients with Malignant Mesothelioma: Topic: Mesothelioma Clinical

2017 Journal of Thoracic Oncology
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The First Report of a Homozygous Codons 9/10 (+T) β-Thalassemia Mutation in a Turkish Patient

2015 Hemoglobin
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Smaller Hippocampus Volume Is Associated with Short Variant of 5-HTTLPR Polymorphism in Medication-Free Major Depressive Disorder Patients

2011 Neuropsychobiology
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The effect of depression, BDNF gene val66met polymorphism and gender on serum BDNF levels

2010 Brain Research Bulletin
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Assessment of clinical and laboratory presentations of familial hemophagocytic lymphohistiocytosis patients with homozygous W374X mutation

2010 Leukemia Research
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Disease causing nature of homozygous missense, p.A523D, alteration in the perforin gene.

2009 Leukemia Research
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ALX4 dysfunction disrupts craniofacial and epidermal development

2009 Human Molecular Genetics
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Neonatal primary hemophagocytic lymphohistiocytosis in Turkish children.

2008 Journal of Pediatric Hematology Oncology
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Clinical and molecular aspects of Turkish familial hemophagocytic lymphohistiocytosis patients with perforin mutations

2008 Leukemia Research
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