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Homozygous c.130–131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry

Pediatric blood & cancer, 2019-10, Vol.66 (10), p.e27923-n/a

2019

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HAX1 mutation positive children presenting with haemophagocytic lymphohistiocytosis

British journal of haematology, 2017-05, Vol.177 (4), p.597-600

2017

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Why G6PD Deficiency Should Be Screened Before COVID-19 Treatment With Hydroxychloroquine?

Journal of pediatric hematology/oncology, 2021-01, Vol.43 (1), p.35

2021

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A Retrospective Analysis of Clinical Characteristics, Treatment Modalities and Outcome of the Patients With Infantile Hepatic Hemangiomas: Single-center Experience From Turkey

Journal of pediatric hematology/oncology, 2023-03, Vol.45 (2), p.e259

2023

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Evaluation of Bleeding Phenotype of Inherited Factor VII Deficiency in Children With a Bleeding Assessment Tool and Global Assays

Journal of pediatric hematology/oncology, 2020-08, Vol.42 (6), p.e527

2020

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Efficacy of Teicoplanin Lock Therapy in the Treatment of Port-related Coagulase-negative Staphylococci Bacteremia in Pediatric Oncology Patients

Journal of pediatric hematology/oncology, 2023-01, Vol.45 (1), p.e17

2023

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Identification of a Novel Mutation in the SEC23B Gene Associated With Congenital Dyserythropoietic Anemia Type II Through the Use of Next-generation Sequencing Panel in an Undiagnosed Case of Nonimmune Hereditary Hemolytic Anemia

Journal of pediatric hematology/oncology, 2018-10, Vol.40 (7), p.e421-e423

2018

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A 3-Year Retrospective Study of the Epidemiology of Acute Respiratory Viral Infections in Pediatric Patients With Cancer Undergoing Chemotherapy

Journal of pediatric hematology/oncology, 2019-05, Vol.41 (4), p.e242

2019

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A New Homozygous Mutation (c.393-394del TA/c.393-394del TA) in the NT5C3 Gene Associated With Pyrimidine-5'-Nucleotidase Deficiency: A Case Report

Journal of pediatric hematology/oncology, 2019-11, Vol.41 (8), p.e484

2019

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Assessment of Serum Galactomannan Test Results of Pediatric Patients With Hematologic Malignancies According to Consecutive Positivity and Threshold Level in Terms of Invasive Aspergillosis Diagnosis: Cross-Sectional Research in a Tertiary Care Hospital

Journal of pediatric hematology/oncology, 2020-07, Vol.42 (5), p.e271

2020

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Aplastic Anemia as an Immune-mediated Complication of Thymoma: A Case Report

Journal of pediatric hematology/oncology, 2018-10, Vol.40 (7), p.e464-e466

2018

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Retrospective analysis of rituximab therapy and splenectomy in childhood chronic and refractory immune thrombocytopenic purpura

Blood coagulation & fibrinolysis, 2016-06, Vol.27 (4), p.431-435

2016

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HAX 1 mutation positive children presenting with haemophagocytic lymphohistiocytosis

British journal of haematology, 2017-05, Vol.177 (4), p.597-600

2017

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Chronic Neutropenia in Childhood: Experience From a Single Center

Journal of pediatric hematology/oncology, 2016-01, Vol.38 (1), p.e35-e38

2016

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Torticollis in a haemophilic infant with inhibitor: a case of spinal epidural haematoma

Blood coagulation & fibrinolysis, 2016-07, Vol.27 (5), p.576-579

2016

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Multicentric plasma cell type of castleman disease in a child: difficulty in diagnosis and treatment

Journal of pediatric hematology/oncology, 2013-10, Vol.35 (7), p.e306-e308

2013

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Infantile-onset thiamine responsive megaloblastic anemia syndrome with SLC19A2 mutation: a case report

Archivos argentinos de pediatría, 2017-06, Vol.115 (3), p.e153-e156

2017

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Síndrome de anemia megaloblástica sensible a la tiamina de aparición en la niñez, con mutación en el genSLC19A2: caso clínico

Archivos argentinos de pediatría, 2017-06, Vol.115 (3), p.e153-e156

2017

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Assessment of Self-Image With the Offer Self-Image Questionnaire in Adolescents With Hemophilia: A Single-Center Experience

Journal of pediatric hematology/oncology, 2020-04, Vol.42 (3), p.e159

2020

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The investigation of relationship between joint findings and serum angiogenic and inflammatory factor levels in severe hemophilia A patients

Blood coagulation & fibrinolysis, 2014-10, Vol.25 (7), p.703-708

2014

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Hepatitis-Associated Aplastic Anemia: Etiology, Clinical Characteristics and Outcome

Journal of pediatric hematology/oncology, 2022-01, Vol.44 (1), p.e223

2022

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Homozygous c.130–131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry

HAX1 mutation positive children presenting with haemophagocytic lymphohistiocytosis

Why G6PD Deficiency Should Be Screened Before COVID-19 Treatment With Hydroxychloroquine?

A Retrospective Analysis of Clinical Characteristics, Treatment Modalities and Outcome of the Patients With Infantile Hepatic Hemangiomas: Single-center Experience From Turkey

Evaluation of Bleeding Phenotype of Inherited Factor VII Deficiency in Children With a Bleeding Assessment Tool and Global Assays

Efficacy of Teicoplanin Lock Therapy in the Treatment of Port-related Coagulase-negative Staphylococci Bacteremia in Pediatric Oncology Patients

Identification of a Novel Mutation in the SEC23B Gene Associated With Congenital Dyserythropoietic Anemia Type II Through the Use of Next-generation Sequencing Panel in an Undiagnosed Case of Nonimmune Hereditary Hemolytic Anemia

A 3-Year Retrospective Study of the Epidemiology of Acute Respiratory Viral Infections in Pediatric Patients With Cancer Undergoing Chemotherapy

A New Homozygous Mutation (c.393-394del TA/c.393-394del TA) in the NT5C3 Gene Associated With Pyrimidine-5'-Nucleotidase Deficiency: A Case Report

Assessment of Serum Galactomannan Test Results of Pediatric Patients With Hematologic Malignancies According to Consecutive Positivity and Threshold Level in Terms of Invasive Aspergillosis Diagnosis: Cross-Sectional Research in a Tertiary Care Hospital

Aplastic Anemia as an Immune-mediated Complication of Thymoma: A Case Report

Retrospective analysis of rituximab therapy and splenectomy in childhood chronic and refractory immune thrombocytopenic purpura

HAX 1 mutation positive children presenting with haemophagocytic lymphohistiocytosis

Chronic Neutropenia in Childhood: Experience From a Single Center

Torticollis in a haemophilic infant with inhibitor: a case of spinal epidural haematoma

Multicentric plasma cell type of castleman disease in a child: difficulty in diagnosis and treatment

Infantile-onset thiamine responsive megaloblastic anemia syndrome with SLC19A2 mutation: a case report

Síndrome de anemia megaloblástica sensible a la tiamina de aparición en la niñez, con mutación en el genSLC19A2: caso clínico

Assessment of Self-Image With the Offer Self-Image Questionnaire in Adolescents With Hemophilia: A Single-Center Experience

The investigation of relationship between joint findings and serum angiogenic and inflammatory factor levels in severe hemophilia A patients

Turkish National Severe Congenital Neutropenia Registry

Hepatitis-Associated Aplastic Anemia: Etiology, Clinical Characteristics and Outcome

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