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Effect of pyridoxine plus pyridostigmine treatment on vincristine-induced peripheral neuropathy in pediatric patients with acute lymphoblastic leukemia: a single-center experience

Neurological sciences, 2021-09, Vol.42 (9), p.3681-3686

2021

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A hidden burden of disease in a specific group: Evaluation of COVID-19 seroconversion rates in pediatric patients with leukemia

American journal of infection control, 2024-03, Vol.52 (3), p.320-323

2024

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Hematopoietic stem cell transplantation with reduced toxicity conditioning regimen in mitochondrial neurogastrointestinal encephalopathy syndrome

Pediatric blood & cancer, 2023-07, Vol.70 (7), p.e30334-n/a

2023

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Successful Management of l-Asparaginase–Associated Pancreatitis With Octreotide and Pegylated Asparaginase in 2 Patients With Acute Lymphoblastic Leukemia: Is There a Different Rare Warning Sign of Hypoglycemia for l-Asparaginase–Associated Pancreatitis?

Clinical therapeutics, 2020-04, Vol.42 (4), p.e82-e86

2020

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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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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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Cerebral Involvement of Hemophagocytic Lymphohistiocytosis in Griscelli Syndrome

The journal of pediatric research, 2019-09, Vol.6 (3), p.252-255

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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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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Identification of novel TUBB1 variants in patients with macrothrombocytopenia

Turkish journal of medical sciences, 2021-04, Vol.51 (2), p.490-500

2021

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Evaluation of renal effects of liposomal amphotericin B in children with malignancies with KDIGO and RIFLE criteria

Néphrologie & thérapeutique, 2021-12, Vol.17 (7), p.507-511

2021

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Children with chronic-refractory autoimmune cytopenias: a single center experience

Turkish journal of pediatrics, 2020-07, Vol.62 (4), p.525-532

2020

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Acrocallosal Syndrome First Presenting with Acute Lymphoblastic Leukemia: A Rare Case Report

Neurology India, 2019-09, Vol.67 (5), p.1386-1387

2019

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Idiopathic Pulmonary Hemosiderosis Mimicking Iron Deficiency Anemia: A Delayed Diagnosis?

Hematology reports, 2017-06, Vol.9 (2), p.7048-7048

2017

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Deferasirox in children with transfusion‐dependent thalassemia or sickle cell anemia: A large cohort real‐life experience from Turkey (REACH‐THEM)

European journal of haematology, 2019-02, Vol.102 (2), p.123-130

2019

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Quality of Life and Depression in Turkish Patients with β-Thalassemia Major: A Cross-Sectional Study

Hemoglobin, 2018-11, Vol.42 (5-6), p.326-329

2018

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Factor 8 Gene Mutation Spectrum of 270 Patients with Hemophilia A: Identification of 36 Novel Mutations

Turkish journal of haematology, 2020-01, Vol.37 (3), p.145-153

2020

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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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Hemoglobin H Disease in Turkey: Experience from Eight Centers

Turkish journal of haematology, 2016-03, Vol.33 (1), p.56-59

2016

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Severe eyelid injury resulting from necrotic arachnidism in a child with leukemia

Canadian journal of ophthalmology, 2013-12, Vol.48 (6), p.e164-e166

2013

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Thrombolysis with Systemic Recombinant Tissue Plasminogen Activator in Children: A Multicenter Retrospective Study

Turkish journal of haematology, 2021-01, Vol.38 (4), p.294-305

2021

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Child with RET proto-oncogene codon 634 mutation

Turkish journal of pediatrics, 2017, Vol.59 (5), p.590-593

2017

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Congenital amegakaryocytic thrombocytopenia: three case reports from patients with different clinical diagnoses and somatic abnormalities

Blood coagulation & fibrinolysis, 2015-04, Vol.26 (3), p.337-341

2015

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Effect of pyridoxine plus pyridostigmine treatment on vincristine-induced peripheral neuropathy in pediatric patients with acute lymphoblastic leukemia: a single-center experience

A hidden burden of disease in a specific group: Evaluation of COVID-19 seroconversion rates in pediatric patients with leukemia

Hematopoietic stem cell transplantation with reduced toxicity conditioning regimen in mitochondrial neurogastrointestinal encephalopathy syndrome

Successful Management of l-Asparaginase–Associated Pancreatitis With Octreotide and Pegylated Asparaginase in 2 Patients With Acute Lymphoblastic Leukemia: Is There a Different Rare Warning Sign of Hypoglycemia for l-Asparaginase–Associated Pancreatitis?

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

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

Cerebral Involvement of Hemophagocytic Lymphohistiocytosis in Griscelli Syndrome

HAX1 mutation positive children presenting with haemophagocytic lymphohistiocytosis

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

Identification of novel TUBB1 variants in patients with macrothrombocytopenia

Evaluation of renal effects of liposomal amphotericin B in children with malignancies with KDIGO and RIFLE criteria

Children with chronic-refractory autoimmune cytopenias: a single center experience

Acrocallosal Syndrome First Presenting with Acute Lymphoblastic Leukemia: A Rare Case Report

Idiopathic Pulmonary Hemosiderosis Mimicking Iron Deficiency Anemia: A Delayed Diagnosis?

Deferasirox in children with transfusion‐dependent thalassemia or sickle cell anemia: A large cohort real‐life experience from Turkey (REACH‐THEM)

Quality of Life and Depression in Turkish Patients with β-Thalassemia Major: A Cross-Sectional Study

Factor 8 Gene Mutation Spectrum of 270 Patients with Hemophilia A: Identification of 36 Novel Mutations

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

Chronic Neutropenia in Childhood: Experience From a Single Center

Hemoglobin H Disease in Turkey: Experience from Eight Centers

Severe eyelid injury resulting from necrotic arachnidism in a child with leukemia

Thrombolysis with Systemic Recombinant Tissue Plasminogen Activator in Children: A Multicenter Retrospective Study

Child with RET proto-oncogene codon 634 mutation

Congenital amegakaryocytic thrombocytopenia: three case reports from patients with different clinical diagnoses and somatic abnormalities

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