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Neonates born to mothers with immune thrombocytopenic purpura: a single-center experience of 20 years

Blood coagulation & fibrinolysis, 2016-01, Vol.27 (1), p.19-23

2016

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A novel mutation in protein C gene (PROC) causing severe phenotype in neonatal period

Pediatric blood & cancer, 2014-04, Vol.61 (4), p.763-764

2014

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Successful Outcome With Fludarabine-Based Conditioning Regimen for Hematopoietic Stem Cell Transplantation From Related Donor in Fanconi Anemia: A Single Center Experience From Turkey

Pediatric blood & cancer, 2016-04, Vol.63 (4), p.695-700

2016

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Infant lymphoblastic leukemia: a single centers 10 year experience

Turkish journal of pediatrics, 2019, Vol.61 (3), p.325-329

2019

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LAD-1/variant syndrome is caused by mutations in FERMT3

Blood, 2009-05, Vol.113 (19), p.4740-4746

2009

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Malignancy-associated hemophagocytic lymphohistiocytosis in pediatric cases: a multicenter study from Turkey

Turkish journal of pediatrics, 2009-05, Vol.51 (3), p.207-213

2009

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Effects of blood transfusion on cytokine profile and pulmonary function in patients with thalassemia major

The clinical respiratory journal, 2016-03, Vol.10 (2), p.153-162

2016

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Plasma sphingomyelin levels were negatively correlated with ferritin levels in splenectomized thalassemia patients

American journal of clinical pathology, 2024-10, Vol.162 (Supplement_1), p.S186-S187

2024

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The Importance of the M470V Polymorphism

Izmir Dr. Behçet Uz Çocuk Hastanesi dergisi, 2017

2017

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Acute Megakaryoblastic Leukemia with t(1;22) Mimicking Neuroblastoma in an Infant

Turkish journal of haematology, 2015-03, Vol.32 (1), p.64-67

2015

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Pyruvate Kinase Deficiency Cases Mimicking Congenital Dyserythropoietic Anemia

Blood, 2019-11, Vol.134 (Supplement_1), p.4794-4794

2019

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Multi‐gene panel testing improves diagnosis and management of patients with hereditary anemias

American journal of hematology, 2018-05, Vol.93 (5), p.672-682

2018

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A randomized, placebo-controlled, double-blind trial of canakinumab in children and young adults with sickle cell anemia

Blood, 2022-04, Vol.139 (17), p.2642-2652

2022

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Dual-echo TFE MRI for the assessment of myocardial iron overload in beta-thalassemia major patients

Diagnostic and interventional radiology (Ankara, Turkey), 2010-03, Vol.16 (1), p.59-62

2010

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Diagnosis: Melanoderma after Hematopoietic Stem Cell Transplantation

Turkish journal of haematology, 2015-12, Vol.32 (4), p.378-379

2015

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Isolated CNS Hemophagocytic Lymphohistiocytosis in Children:What We Know, What We Don't Know ?

Blood, 2021-11, Vol.138 (Supplement 1), p.4190-4190

2021

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A rare metabolic complication of acute lymphoblastic leukemia in childhood: lactic acidosis

Turkish journal of pediatrics, 2012-01, Vol.54 (1), p.61-63

2012

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Retrospective cohort study of 205 cases with congenital dyserythropoietic anemia type II: Definition of clinical and molecular spectrum and identification of new diagnostic scores

American journal of hematology, 2014-10, Vol.89 (10), p.E169-E175

2014

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Molecular Analyses of Pyruvate Kinase Deficient Turkish Patients from a Single Center

Pediatric hematology and oncology, 2015-07, Vol.32 (5), p.354-361

2015

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The role of vascular inflammation markers in deficiency of adenosine deaminase 2

Seminars in arthritis and rheumatism, 2021-08, Vol.51 (4), p.839-844

2021

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The Outcome of Modified St. Jude Total XV Protocol in Turkish Children with Newly Diagnosed Acute Lymphoblastic Leukemia

Blood, 2019-11, Vol.134 (Supplement_1), p.2590-2590

2019

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Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond-like features

The Journal of clinical investigation, 2017-11, Vol.127 (11), p.4090-4103

2017

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Mechanism for survival of homozygous nonsense mutations in the tumor suppressor gene BRCA1

Proceedings of the National Academy of Sciences - PNAS, 2018-05, Vol.115 (20), p.5241-5246

2018

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Hematological consequences of pandemic influenza H1N1 infection: a single center experience

Turkish journal of pediatrics, 2010-11, Vol.52 (6), p.570-575

2010

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Neonates born to mothers with immune thrombocytopenic purpura: a single-center experience of 20 years

A novel mutation in protein C gene (PROC) causing severe phenotype in neonatal period

Successful Outcome With Fludarabine-Based Conditioning Regimen for Hematopoietic Stem Cell Transplantation From Related Donor in Fanconi Anemia: A Single Center Experience From Turkey

Infant lymphoblastic leukemia: a single centers 10 year experience

LAD-1/variant syndrome is caused by mutations in FERMT3

Malignancy-associated hemophagocytic lymphohistiocytosis in pediatric cases: a multicenter study from Turkey

Effects of blood transfusion on cytokine profile and pulmonary function in patients with thalassemia major

Plasma sphingomyelin levels were negatively correlated with ferritin levels in splenectomized thalassemia patients

The Importance of the M470V Polymorphism

Acute Megakaryoblastic Leukemia with t(1;22) Mimicking Neuroblastoma in an Infant

Pyruvate Kinase Deficiency Cases Mimicking Congenital Dyserythropoietic Anemia

Multi‐gene panel testing improves diagnosis and management of patients with hereditary anemias

A randomized, placebo-controlled, double-blind trial of canakinumab in children and young adults with sickle cell anemia

Dual-echo TFE MRI for the assessment of myocardial iron overload in beta-thalassemia major patients

Diagnosis: Melanoderma after Hematopoietic Stem Cell Transplantation

Isolated CNS Hemophagocytic Lymphohistiocytosis in Children:What We Know, What We Don't Know ?

A rare metabolic complication of acute lymphoblastic leukemia in childhood: lactic acidosis

Retrospective cohort study of 205 cases with congenital dyserythropoietic anemia type II: Definition of clinical and molecular spectrum and identification of new diagnostic scores

Molecular Analyses of Pyruvate Kinase Deficient Turkish Patients from a Single Center

The role of vascular inflammation markers in deficiency of adenosine deaminase 2

The Outcome of Modified St. Jude Total XV Protocol in Turkish Children with Newly Diagnosed Acute Lymphoblastic Leukemia

Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond-like features

Comparison of primary human cytotoxic T-cell and natural killer cell responses reveal similar molecular requirements for lytic granule exocytosis but differences in cytokine production

Mechanism for survival of homozygous nonsense mutations in the tumor suppressor gene BRCA1

Hematological consequences of pandemic influenza H1N1 infection: a single center experience

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