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Myeloid sarcoma with RBM15::MRTFA (MKL1) mimicking vascular neoplasm

Virchows Archiv : an international journal of pathology, 2024-02

2024

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Outcome of the Modified St. Jude Total XV Protocol in Turkish Children with Newly Diagnosed Acute Lymphoblastic Leukemia: A Single-Center Retrospective Analysis

Turkish journal of haematology, 2024-08, Vol.41 (3), p.146-159

2024

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COVID‐19‐related multiple inflammatory syndrome‐C and pulmonary embolism in Aicardi–Goutries syndrome

Pediatric pulmonology, 2023-11, Vol.58 (11), p.3326-3329

2023

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Pharmacology, Efficacy and Safety of a Triple-Secured Fibrinogen Concentrate in Children Less than or Equal to 12 Years with Afibrinogenaemia

Thrombosis and haemostasis, 2020-06, Vol.120 (6), p.957-967

2020

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Autoinflammation in addition to combined immunodeficiency: SLC29A3 gene defect

Molecular immunology, 2020-05, Vol.121, p.28-37

2020

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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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A rare form of congenital neutropenia: VPS45 deficiency

Scandinavian journal of immunology, 2020-05, Vol.91 (5), p.e12871-n/a

2020

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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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PB1747: OUTCOME OF CHILDHOOD ALLTREATED WITH ALL BFM IC 2009 PROTOCOL

HemaSphere, 2023-08, Vol.7 (S3), p.e567108f-n/a

2023

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Gene therapy in haemophilia: literature review and regional perspectives for Turkey

Therapeutic Advances in Hematology, 2022, Vol.13, p.20406207221104591-20406207221104591

2022

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Adenosine Deaminase Type II Deficiency: Severe Chronic Neutropenia, Lymphoid Infiltration in Bone Marrow, and Inflammatory Features

Immunological investigations, 2022-04, Vol.51 (3), p.558-566

2022

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Hypereosinophilic Syndrome: Hacettepe Experience

Journal of pediatric hematology/oncology, 2016-10, Vol.38 (7), p.539-543

2016

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Clinical Evaluation of Balance in Children With Hemophilic Arthropathy

Indian journal of hematology & blood transfusion, 2022-10, Vol.38 (4), p.698-702

2022

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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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Foetal and neonatal intracranial haemorrhage in term newborn infants: Hacettepe University experience

Blood coagulation & fibrinolysis, 2016-03, Vol.27 (2), p.163-168

2016

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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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Molecular genetic analysis of the F11 gene in 14 Turkish patients with factor XI deficiency: identification of novel and recurrent mutations and their inheritance within families

Blood transfusion = Trasfusione del sangue, 2018-01, Vol.16 (1), p.105-113

2018

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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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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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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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Nonradioactive Vitamin B12 Absorption Test Evaluated in Controls and in Patients with Inherited Malabsorption of Vitamin B12

Clinical chemistry (Baltimore, Md.), 2005-11, Vol.51 (11), p.2151-2155

2005

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Anaphylactic reaction to polyethylene‐glycol conjugated‐asparaginase: Premedication and desensitization may not be sufficient

Pediatrics international, 2013-08, Vol.55 (4), p.531-533

2013

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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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Myeloid sarcoma with RBM15::MRTFA (MKL1) mimicking vascular neoplasm

Outcome of the Modified St. Jude Total XV Protocol in Turkish Children with Newly Diagnosed Acute Lymphoblastic Leukemia: A Single-Center Retrospective Analysis

COVID‐19‐related multiple inflammatory syndrome‐C and pulmonary embolism in Aicardi–Goutries syndrome

Pharmacology, Efficacy and Safety of a Triple-Secured Fibrinogen Concentrate in Children Less than or Equal to 12 Years with Afibrinogenaemia

Autoinflammation in addition to combined immunodeficiency: SLC29A3 gene defect

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

A rare form of congenital neutropenia: VPS45 deficiency

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

PB1747: OUTCOME OF CHILDHOOD ALLTREATED WITH ALL BFM IC 2009 PROTOCOL

Gene therapy in haemophilia: literature review and regional perspectives for Turkey

Adenosine Deaminase Type II Deficiency: Severe Chronic Neutropenia, Lymphoid Infiltration in Bone Marrow, and Inflammatory Features

Hypereosinophilic Syndrome: Hacettepe Experience

Clinical Evaluation of Balance in Children With Hemophilic Arthropathy

Fanconi anemia: a single center experience of a large cohort

Hb H Disease Diagnosed During Adolescent Pregnancy

Foetal and neonatal intracranial haemorrhage in term newborn infants: Hacettepe University experience

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

Molecular genetic analysis of the F11 gene in 14 Turkish patients with factor XI deficiency: identification of novel and recurrent mutations and their inheritance within families

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

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

Infant lymphoblastic leukemia: a single centers 10 year experience

Nonradioactive Vitamin B12 Absorption Test Evaluated in Controls and in Patients with Inherited Malabsorption of Vitamin B12

Anaphylactic reaction to polyethylene‐glycol conjugated‐asparaginase: Premedication and desensitization may not be sufficient

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

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