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Preparation and characterization of polymer-coated mesoporous silica nanoparticles and their application in Subtilisin immobilization

Korean Journal of Chemical Engineering, 2017, 34(7), 208, pp.1992-2001

2017

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Comment on: Clinical, cytogenetic, and molecular analyses of 17 neonates with transient abnormal myelopoiesis and nonconstitutional trisomy 21

Pediatric blood & cancer, 2020-11, Vol.67 (11), p.e28289-n/a

2020

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Changing Disease Course of Crimean-Congo Hemorrhagic Fever in Children, Turkey

Emerging infectious diseases, 2023-02, Vol.29 (2), p.268-277

2023

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A rare case of Klippel-Trenaunay syndrome presenting with chronic myeloid leukemia

The Turkish journal of pediatrics, 2023-01, Vol.65 (1), p.124-128

2023

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The remarkable response to ponatinib therapy in a child with blastic phase of chronic myeloid leukemia

Turkish journal of pediatrics, 2020-05, Vol.62 (3), p.479-481

2020

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Correction to: Multiparametric analysis of etoposide exposed mesenchymal stem cells and Fanconi anemia cells: implications in development of secondary myeloid malignancy

Clinical and experimental medicine, 2023-12, Vol.23 (8), p.4525-4525

2023

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Vacuolization in Myeloid and Erythroid Precursors in a Child with Menkes Disease

Turkish journal of haematology, 2019-08, Vol.36 (3), p.203-204

2019

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Multiparametric analysis of etoposide exposed mesenchymal stem cells and Fanconi anemia cells: implications in development of secondary myeloid malignancy

Clinical and experimental medicine, 2023-12, Vol.23 (8), p.4511-4524

2023

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Rare Cytogenetic Anomalies in Two Pediatric Patients with Acute Leukemia

Turkish journal of haematology, 2020-01, Vol.37 (2), p.132-133

2020

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PB1727: EVALUATION OF POST‐TREATMENT SECONDARY CANCERS IN CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKEMIA TREATED WITH MODIFIED ST. JUDE TOTAL XIII AND TOTAL XV PROTOCOLS

HemaSphere, 2023-08, Vol.7 (S3), p.e848145b-n/a

2023

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Acute myeloid leukemia in a child with dedicator of cytokinesis 8 (DOCK8) deficiency

Pediatric blood & cancer, 2017-12, Vol.64 (12), p.n/a

2017

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Hereditary Elliptocytosis with Pyropoikilocytosis

Turkish journal of haematology, 2016-03, Vol.33 (1), p.86-87

2016

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The Hematological and Molecular Spectrum of α-Thalassemias in Turkey: The Hacettepe Experience

Turkish journal of haematology, 2015-06, Vol.32 (2), p.136-143

2015

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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

Turkish journal of haematology, 2018, Vol.35 (4), p.229-259

2018

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Fanconi anemia: a single center experience of a large cohort

Turkish journal of pediatrics, 2019, Vol.61 (4), p.477-484

2019

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Hb H Disease Diagnosed During Adolescent Pregnancy

Hemoglobin, 2020-03, Vol.44 (2), p.137-138

2020

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Medical management of moyamoya disease and recurrent stroke in an infant with Majewski osteodysplastic primordial dwarfism type II (MOPD II)

European journal of pediatrics, 2012-10, Vol.171 (10), p.1567-1571

2012

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Serum Lipids in Turkish Patients with β-Thalassemia Major and β-Thalassemia Minor

Turkish journal of haematology, 2016-03, Vol.33 (1), p.72-73

2016

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An Infant With Congenital Leukemia Cutis and AML-M5 With MLL Gene Rearrangement

Journal of pediatric hematology/oncology, 2015-10, Vol.37 (7), p.566-567

2015

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Immune Thrombocytopenic Purpura During Maintenance Phase of Acute Lymphoblastic Leukemia: A Rare Coexistence Requiring a High Degree of Suspicion, a Case Report and Review of the Literature

Turkish journal of haematology, 2015-12, Vol.32 (4), p.363-366

2015

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The questioning for routine monthly monitoring of proteinuria in patients with β-thalassemia on deferasirox chelation

Hematology (Luxembourg), 2017-04, Vol.22 (4), p.248-251

2017

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Glucose-6-phosphate dehydrogenase deficiency in neonatal hyperbilirubinaemia: Hacettepe experıence

Journal of paediatrics and child health, 2013-05, Vol.49 (5), p.399-402

2013

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The relationship between hematological findings and coronary artery aneurysm in kawasaki disease

Turkish journal of haematology, 2014-06, Vol.31 (2), p.199-200

2014

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Preparation and characterization of polymer-coated mesoporous silica nanoparticles and their application in Subtilisin immobilization

Comment on: Clinical, cytogenetic, and molecular analyses of 17 neonates with transient abnormal myelopoiesis and nonconstitutional trisomy 21

Changing Disease Course of Crimean-Congo Hemorrhagic Fever in Children, Turkey

A rare case of Klippel-Trenaunay syndrome presenting with chronic myeloid leukemia

The remarkable response to ponatinib therapy in a child with blastic phase of chronic myeloid leukemia

Correction to: Multiparametric analysis of etoposide exposed mesenchymal stem cells and Fanconi anemia cells: implications in development of secondary myeloid malignancy

Vacuolization in Myeloid and Erythroid Precursors in a Child with Menkes Disease

Multiparametric analysis of etoposide exposed mesenchymal stem cells and Fanconi anemia cells: implications in development of secondary myeloid malignancy

Rare Cytogenetic Anomalies in Two Pediatric Patients with Acute Leukemia

PB1727: EVALUATION OF POST‐TREATMENT SECONDARY CANCERS IN CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKEMIA TREATED WITH MODIFIED ST. JUDE TOTAL XIII AND TOTAL XV PROTOCOLS

A National Registry of Thalassemia in Turkey: Demographic and Disease Characteristics of Patients, Achievements, and Challenges in Prevention

Acute myeloid leukemia in a child with dedicator of cytokinesis 8 (DOCK8) deficiency

Hereditary Elliptocytosis with Pyropoikilocytosis

Outcomes of Eltrombopag Treatment and Development of Iron Deficiency in Children with Immune Thrombocytopenia in Turkey

The Hematological and Molecular Spectrum of α-Thalassemias in Turkey: The Hacettepe Experience

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

Fanconi anemia: a single center experience of a large cohort

Hb H Disease Diagnosed During Adolescent Pregnancy

Medical management of moyamoya disease and recurrent stroke in an infant with Majewski osteodysplastic primordial dwarfism type II (MOPD II)

Serum Lipids in Turkish Patients with β-Thalassemia Major and β-Thalassemia Minor

An Infant With Congenital Leukemia Cutis and AML-M5 With MLL Gene Rearrangement

Immune Thrombocytopenic Purpura During Maintenance Phase of Acute Lymphoblastic Leukemia: A Rare Coexistence Requiring a High Degree of Suspicion, a Case Report and Review of the Literature

The questioning for routine monthly monitoring of proteinuria in patients with β-thalassemia on deferasirox chelation

Glucose-6-phosphate dehydrogenase deficiency in neonatal hyperbilirubinaemia: Hacettepe experıence

The relationship between hematological findings and coronary artery aneurysm in kawasaki disease

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