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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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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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An evaluation of participation restrictions and associated factors via the ICF-CY framework in children with acute lymphoblastic leukemia receiving maintenance chemotherapy

European journal of pediatrics, 2021-04, Vol.180 (4), p.1081-1088

2021

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Central nervous system lesions in Fanconi anemia: Experience from a research center for Fanconi anemia patients

Pediatric blood & cancer, 2020-12, Vol.67 (12), p.e28722-n/a

2020

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

Turkish journal of haematology, 2024-09, Vol.41 (3), p.146-159

2024

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Proerythroblast Cells of Diamond-Blackfan Anemia Patients With RPS19 and CECR1 Mutations Have Similar Transcriptomic Signature

Frontiers in physiology, 2021-06, Vol.12, p.679919-679919

2021

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MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopenia

Blood advances, 2018-03, Vol.2 (6), p.586-596

2018

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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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Assessment of biochemical bone markers of osteoporosis in children with thalassemia major

Italian journal of pediatrics, 2022-06, Vol.48 (1), p.1-105, Article 105

2022

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Oral health status of patients with inherited bone marrow failure syndromes

Pediatric dental journal, 2022-12, Vol.32 (3), p.151-159

2022

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Update on HLH treatment

Leukemia research, 2019-10, Vol.85, p.S18-S19

Unal, Sule

2019

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SP-40 - Update on HLH treatment

Leukemia research, 2019-10, Vol.85, p.S18-S19

Unal, Sule

2019

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Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein

Frontiers in physiology, 2019-05, Vol.10, p.621-621

2019

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Bleeding and non-bleeding phenotypes in patients with GGCX gene mutations

Thrombosis research, 2014-10, Vol.134 (4), p.856-865

2014

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Dominant Beta Thalassemia: A Very Rare Cause of Thalassemia in a Mediterranean Country

Hemoglobin, 2024-08, Vol.48 (4), p.1-260

2024

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Endocrine Disorders in Adult Beta-Thalassemia Patients: Insights from a Long-Term Follow-Up

Endocrinology Research and Practice, 2023-10, Vol.27 (4), p.205-212

2023

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Corrigendum: Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein

Frontiers in physiology, 2020-08, Vol.11, p.940-940

2020

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Atypical combined immunodeficiency due to Artemis defect: A case presenting as hyperimmunoglobulin M syndrome and with LGLL

Molecular immunology, 2013-12, Vol.56 (4), p.354-357

2013

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Recommendations for diagnosis, treatment, and prevention of iron deficiency and iron deficiency anemia

HemaSphere, 2024-07, Vol.8 (7), p.e108-n/a

2024

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Nocturnal enuresis in sickle cell disease and thalassemia major: associated factors in a clinical sample

International journal of hematology, 2013-10, Vol.98 (4), p.430-436

2013

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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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Heavy metal levels in patients with ineffective erythropoiesis

Transfusion and apheresis science, 2017-08, Vol.56 (4), p.539-543

2017

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Refugee children with beta‐thalassemia in Turkey: Overview of demographic, socioeconomic, and medical characteristics

Pediatric blood & cancer, 2019-05, Vol.66 (5), p.e27636-n/a

2019

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

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

An evaluation of participation restrictions and associated factors via the ICF-CY framework in children with acute lymphoblastic leukemia receiving maintenance chemotherapy

Central nervous system lesions in Fanconi anemia: Experience from a research center for Fanconi anemia patients

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

Proerythroblast Cells of Diamond-Blackfan Anemia Patients With RPS19 and CECR1 Mutations Have Similar Transcriptomic Signature

MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopenia

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

Assessment of biochemical bone markers of osteoporosis in children with thalassemia major

Oral health status of patients with inherited bone marrow failure syndromes

Update on HLH treatment

SP-40 - Update on HLH treatment

Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein

Bleeding and non-bleeding phenotypes in patients with GGCX gene mutations

Dominant Beta Thalassemia: A Very Rare Cause of Thalassemia in a Mediterranean Country

Endocrine Disorders in Adult Beta-Thalassemia Patients: Insights from a Long-Term Follow-Up

Corrigendum: Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein

Atypical combined immunodeficiency due to Artemis defect: A case presenting as hyperimmunoglobulin M syndrome and with LGLL

Recommendations for diagnosis, treatment, and prevention of iron deficiency and iron deficiency anemia

Nocturnal enuresis in sickle cell disease and thalassemia major: associated factors in a clinical sample

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

Heavy metal levels in patients with ineffective erythropoiesis

Refugee children with beta‐thalassemia in Turkey: Overview of demographic, socioeconomic, and medical characteristics

Transcobalamin II Deficiency in Four Cases with Novel Mutations

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

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