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Motor and Basic Cognitive Functions in Children with Acute Lymphoblastic Leukemia Undergoing Induction or Consolidation Chemotherapy

Perceptual and motor skills, 2021-06, Vol.128 (3), p.1091-1106

2021

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The clinical and laboratory evaluation of familial hemophagocytic lymphohistiocytosis and the importance of hepatic and spinal cord involvement: a single center experience

Haematologica (Roma), 2018-02, Vol.103 (2), p.231-236

2018

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Clinical and Molecular Spectrum of Glucose-6-Phosphate Isomerase Deficiency. Report of 12 New Cases

Frontiers in physiology, 2019-05, Vol.10, p.467-467

2019

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Case series of thromboembolic complications in childhood nephrotic syndrome: Hacettepe experience

Clinical and experimental nephrology, 2015-06, Vol.19 (3), p.506-513

2015

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A Monogenic Disease with a Variety of Phenotypes: Deficiency of Adenosine Deaminase 2

Journal of rheumatology, 2020-01, Vol.47 (1), p.117-125

2020

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Alternative algorithm for L-asparaginase allergy in children with acute lymphoblastic leukemia

Journal of allergy and clinical immunology, 2009-04, Vol.123 (4), p.895-899

2009

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

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

2009

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Macrophage activation syndrome in children with systemic juvenile idiopathic arthritis and systemic lupus erythematosus

Rheumatology international, 2016-10, Vol.36 (10), p.1421-1429

2016

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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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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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Evaluation of Clinical, Laboratory Findings and Prognosis of Paediatric Thrombosis

Blood, 2017-12, Vol.130, p.4921-4921

2017

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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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Reliability and Validity of the Turkish Version of the PedsQL 3.0 Cancer Module for 2- to 7-Year-Old and the PedsQL 4.0 Generic Core Scales for 5- to 7-Year-Old: The Hacettepe University Experience

Turkish journal of haematology, 2016-09, Vol.33 (3), p.236-243

2016

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Long-Term Outcome of Deferasirox Chelation in Patients with Thalassemia Major

Blood, 2016-12, Vol.128 (22), p.3620-3620

2016

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Assessment of Ecotropic Viral Integration Site 2B (EVI2B) Gene in Juvenile Myelomonocytic Leukemia and Neurofibromatosis Type 1 NF1 Tumors

Biochemical genetics, 2024-04, Vol.62 (2), p.1263-1276

2024

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Sea‐blue histiocytes in the bone marrow of a boy with severe congenital neutropenia associated with G6PC3 mutation

British journal of haematology, 2014-05, Vol.165 (4), p.426-426

2014

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Children with Juvenile Myelomonocytic Leukemia (JMML); A Single Center Experience

Blood, 2018-11, Vol.132 (Supplement 1), p.5527-5527

2018

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Transcobalamin II Deficiency in Four Cases with Novel Mutations

Turkish journal of haematology, 2015-12, Vol.32 (4), p.317-322

2015

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Use of alternative or supportive care products among hematology patients in a pediatric hematology outpatient clinic

Journal of clinical oncology, 2016-05, Vol.34 (15_suppl), p.e21585-e21585

2016

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Kindlin-3–independent adhesion of neutrophils from patients with leukocyte adhesion deficiency type III

Journal of allergy and clinical immunology, 2014-04, Vol.133 (4), p.1215-1218.e3

2014

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Hematological features in children with systemic lupus erythematosus: are they more common than appreciated?

Pediatric rheumatology online journal, 2011-09, Vol.9 (S1), p.P242-P242, Article P242

2011

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Generalized lichen nitidus associated with neurofibromatosis type 1 and juvenile myelomonocytic leukemia

International journal of dermatology, 2016-11, Vol.55 (11), p.e592-e594

2016

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NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet α-granules

Nature genetics, 2011-08, Vol.43 (8), p.732-734

2011

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The neurologic complications in pediatric acute lymphoblastic leukemia patients excluding leukemic infiltration

Leukemia research, 2006-05, Vol.30 (5), p.537-541

2006

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Motor and Basic Cognitive Functions in Children with Acute Lymphoblastic Leukemia Undergoing Induction or Consolidation Chemotherapy

The clinical and laboratory evaluation of familial hemophagocytic lymphohistiocytosis and the importance of hepatic and spinal cord involvement: a single center experience

Clinical and Molecular Spectrum of Glucose-6-Phosphate Isomerase Deficiency. Report of 12 New Cases

Case series of thromboembolic complications in childhood nephrotic syndrome: Hacettepe experience

A Monogenic Disease with a Variety of Phenotypes: Deficiency of Adenosine Deaminase 2

Alternative algorithm for L-asparaginase allergy in children with acute lymphoblastic leukemia

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

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

Macrophage activation syndrome in children with systemic juvenile idiopathic arthritis and systemic lupus erythematosus

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

Rare Cytogenetic Anomalies in Two Pediatric Patients with Acute Leukemia

Evaluation of Clinical, Laboratory Findings and Prognosis of Paediatric Thrombosis

Fanconi anemia: a single center experience of a large cohort

Reliability and Validity of the Turkish Version of the PedsQL 3.0 Cancer Module for 2- to 7-Year-Old and the PedsQL 4.0 Generic Core Scales for 5- to 7-Year-Old: The Hacettepe University Experience

Long-Term Outcome of Deferasirox Chelation in Patients with Thalassemia Major

Assessment of Ecotropic Viral Integration Site 2B (EVI2B) Gene in Juvenile Myelomonocytic Leukemia and Neurofibromatosis Type 1 NF1 Tumors

Sea‐blue histiocytes in the bone marrow of a boy with severe congenital neutropenia associated with G6PC3 mutation

Children with Juvenile Myelomonocytic Leukemia (JMML); A Single Center Experience

Transcobalamin II Deficiency in Four Cases with Novel Mutations

Use of alternative or supportive care products among hematology patients in a pediatric hematology outpatient clinic

Kindlin-3–independent adhesion of neutrophils from patients with leukocyte adhesion deficiency type III

Hematological features in children with systemic lupus erythematosus: are they more common than appreciated?

Generalized lichen nitidus associated with neurofibromatosis type 1 and juvenile myelomonocytic leukemia

NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet α-granules

The neurologic complications in pediatric acute lymphoblastic leukemia patients excluding leukemic infiltration

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