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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

2020

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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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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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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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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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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

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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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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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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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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Familial Multiple Coagulation Factor Deficiencies (FMCFDs) in a Large Cohort of Patients-A Single-Center Experience in Genetic Diagnosis

Journal of clinical medicine, 2021-01, Vol.10 (2), p.347

2021

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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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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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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 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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Successful Outcome With Fludarabine-Based Conditioning Regimen for Hematopoietic Stem Cell Transplantation From Related Donor in Fanconi Anemia: A Single Center Experience From Turkey

Pediatric blood & cancer, 2016-04, Vol.63 (4), p.695-700

2016

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

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

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

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

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

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

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

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

Heavy metal levels in patients with ineffective erythropoiesis

Familial Multiple Coagulation Factor Deficiencies (FMCFDs) in a Large Cohort of Patients-A Single-Center Experience in Genetic Diagnosis

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

Transcobalamin II Deficiency in Four Cases with Novel Mutations

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

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

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

Successful Outcome With Fludarabine-Based Conditioning Regimen for Hematopoietic Stem Cell Transplantation From Related Donor in Fanconi Anemia: A Single Center Experience From Turkey

Infant lymphoblastic leukemia: a single centers 10 year experience

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