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T helper, cytotoxic T, and natural killer T cell profiles and their association with clinical prognosis in children with sickle cell anemia

Cukurova Medical Journal, 2018-12, Vol.43 (4), p.1002-1007

2018

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Effects of deferasirox-deferoxamine on myocardial and liver iron in patients with severe transfusional iron overload

Blood, 2015-06, Vol.125 (25), p.3868-3877

2015

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A 1-year randomized controlled trial of deferasirox vs deferoxamine for myocardial iron removal in β-thalassemia major (CORDELIA)

Blood, 2014-03, Vol.123 (10), p.1447-1454

2014

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THE ICET-A SURVEY ON CURRENT CRITERIA USED BY CLINICIANS FOR THE ASSESSMENT OF CENTRAL ADRENAL INSUFFICIENCY IN THALASSEMIA: ANALYSIS OF RESULTS AND RECOMMENDATIONS

Mediterranean journal of hematology and infectious diseases, 2016-07, Vol.8 (1), p.e2016034-e2016034

De Sanctis, Vincenzo

2016

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Membranous nephropathy presenting with nephrotic syndrome in a child with thalassemia major

Pediatrics international, 2015-08, Vol.57 (4), p.711-713

2015

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Prevalence and distribution of iron overload in patients with transfusion-dependent anemias differs across geographic regions: results from the CORDELIA study

European journal of haematology, 2015-09, Vol.95 (3), p.244-253

2015

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Juvenile Myelomonocytic Leukemia (JMML)

The journal of pediatric research, 2014-09, Vol.1 (3), p.118-126

2014

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Sustained improvements in myocardial T2 over 2 years in severely iron‐overloaded patients with beta thalassemia major treated with deferasirox or deferoxamine

American journal of hematology, 2015-02, Vol.90 (2), p.91-96

2015

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Microparticle Profile During Painful Crisis and Steady State Period In Sickle Cell Anemia

Blood, 2013-11, Vol.122 (21), p.4681-4681

2013

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Deep Vein Thrombosis After a Wild Bee Sting

Journal of pediatric hematology/oncology, 2022-01, Vol.44 (1), p.e241-e242

2022

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Homozygous c.130–131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry

Pediatric blood & cancer, 2019-10, Vol.66 (10), p.e27923-n/a

2019

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A randomized, placebo-controlled, double-blind trial of canakinumab in children and young adults with sickle cell anemia

Blood, 2022-04, Vol.139 (17), p.2642-2652

2022

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Silent cerebral infarct in sickle cell anemia patients of southern Turkey

TURKISH JOURNAL OF MEDICAL SCIENCES, 2020-12, Vol.50 (8), p.1887-1893

2020

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Management of Life-Threatening Hemorrhages and Unsafe Interventions in Nonhemophiliac Children by Recombinant Factor VIIa

Clinical and applied thrombosis/hemostasis, 2010-02, Vol.16 (1), p.77-82

2010

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Stroke in a Pediatric Immune Thrombocytopenia Case

Blood, 2018-11, Vol.132 (Supplement 1), p.5008-5008

2018

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P308 Analysis of genitourinary anomalies in patients with fanconi aplastic anaemia

Archives of disease in childhood, 2017-06, Vol.102 (Suppl 2), p.A152-A152

2017

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Iron chelation with deferasirox in adult and pediatric patients with thalassemia major: efficacy and safety during 5 years' follow-up

Blood, 2011-07, Vol.118 (4), p.884-893

2011

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Iliopsoas Hematoma in a Child with Factor XIII Deficiency

Blood, 2017-12, Vol.130, p.4876-4876

2017

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Endocrine Complications in Thalassemia Major

Blood, 2017-12, Vol.130, p.4759-4759

2017

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Deferasirox Decreases Liver Iron Concentration in Iron-Overloaded Patients with Myelodysplastic Syndromes, Aplastic Anemia and Other Rare Anemias

Acta haematologica, 2015-01, Vol.134 (4), p.233-242

2015

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Efficacy and Safety of Sevuparin, a Novel Non-Anti-Coagulant Heparinoid, in Patients with Acute Painful Vaso-Occlusive Crisis; A Global, Multicenter Double-Blind, Randomized, Placebo-Controlled Phase 2 Trial (TVOC01)

Blood, 2019-11, Vol.134 (Supplement_1), p.614-614

2019

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Evaluation of endocrine complications in beta-thalassemia intermedia (β-TI): a cross-sectional multicenter study

An ICET-A survey on occult and emerging endocrine complications in patients with β-thalassemia major: Conclusions and recommendations

T helper, cytotoxic T, and natural killer T cell profiles and their association with clinical prognosis in children with sickle cell anemia

Effects of deferasirox-deferoxamine on myocardial and liver iron in patients with severe transfusional iron overload

A 1-year randomized controlled trial of deferasirox vs deferoxamine for myocardial iron removal in β-thalassemia major (CORDELIA)

THE ICET-A SURVEY ON CURRENT CRITERIA USED BY CLINICIANS FOR THE ASSESSMENT OF CENTRAL ADRENAL INSUFFICIENCY IN THALASSEMIA: ANALYSIS OF RESULTS AND RECOMMENDATIONS

Membranous nephropathy presenting with nephrotic syndrome in a child with thalassemia major

Prevalence and distribution of iron overload in patients with transfusion-dependent anemias differs across geographic regions: results from the CORDELIA study

Juvenile Myelomonocytic Leukemia (JMML)

Sustained improvements in myocardial T2 over 2 years in severely iron‐overloaded patients with beta thalassemia major treated with deferasirox or deferoxamine

Microparticle Profile During Painful Crisis and Steady State Period In Sickle Cell Anemia

Deep Vein Thrombosis After a Wild Bee Sting

Homozygous c.130–131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry

A randomized, placebo-controlled, double-blind trial of canakinumab in children and young adults with sickle cell anemia

Silent cerebral infarct in sickle cell anemia patients of southern Turkey

Management of Life-Threatening Hemorrhages and Unsafe Interventions in Nonhemophiliac Children by Recombinant Factor VIIa

A National Registry of Thalassemia in Turkey: Demographic and Disease Characteristics of Patients, Achievements, and Challenges in Prevention

Stroke in a Pediatric Immune Thrombocytopenia Case

P308 Analysis of genitourinary anomalies in patients with fanconi aplastic anaemia

Iron chelation with deferasirox in adult and pediatric patients with thalassemia major: efficacy and safety during 5 years' follow-up

Iliopsoas Hematoma in a Child with Factor XIII Deficiency

Endocrine Complications in Thalassemia Major

Deferasirox Decreases Liver Iron Concentration in Iron-Overloaded Patients with Myelodysplastic Syndromes, Aplastic Anemia and Other Rare Anemias

Efficacy and Safety of Sevuparin, a Novel Non-Anti-Coagulant Heparinoid, in Patients with Acute Painful Vaso-Occlusive Crisis; A Global, Multicenter Double-Blind, Randomized, Placebo-Controlled Phase 2 Trial (TVOC01)

A phase 3 study of deferasirox (ICL670), a once-daily oral iron chelator, in patients with β-thalassemia

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