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Thalassemia major patients using iron chelators showed a reduced plasma thioredoxin level and reduced thioredoxin reductase activity, despite elevated oxidative stress

Free radical research, 2015-03, Vol.49 (3), p.309-316

2015

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A Phase 3 Randomized Trial of Voxelotor in Sickle Cell Disease

The New England journal of medicine, 2019-08, Vol.381 (6), p.509-519

2019

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Alterations of panoramic radiomorphometric indices in children and adolescents with beta-thalassemia major: A fractal analysis study

Medicina oral, patología oral y cirugía bucal, 2022-01, Vol.27 (1), p.e10-e17

2022

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Establishing a harmonized haemophilia registry for countries with developing health care systems

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-09, Vol.19 (5), p.668-673

2013

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Safety of dabigatran etexilate for the secondary prevention of venous thromboembolism in children

Blood, 2020-02, Vol.135 (7), p.491-504

2020

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The value of early treatment in patients with haemophilia and inhibitors

Haemophilia : the official journal of the World Federation of Hemophilia, 2010-05, Vol.16 (3), p.487-494

2010

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Successful hematopoietic SCT from non-identical twins to two sisters with β-thalassemia major by using preimplantation genetic diagnosis and HLA typing

Bone marrow transplantation (Basingstoke), 2011-12, Vol.46 (12), p.1581-1582

2011

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Prophylaxis vs. on‐demand treatment with BAY 81‐8973, a full‐length plasma protein‐free recombinant factor VIII product: results from a randomized trial (LEOPOLD II)

Journal of thrombosis and haemostasis, 2015-03, Vol.13 (3), p.360-369

2015

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Chemotherapy for transient myeloproliferative disorder in a premature infant with Down syndrome

Journal of clinical pharmacy and therapeutics, 2013-06, Vol.38 (3), p.262-264

2013

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Plasma homocysteine levels in patients with β-thalassaemia major

Scandinavian journal of clinical and laboratory investigation, 2008-01, Vol.68 (2), p.134-139

2008

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Recombinant factor VIIa analog in the management of hemophilia with inhibitors: results from a multicenter, randomized, controlled trial of vatreptacog alfa

Journal of thrombosis and haemostasis, 2014-08, Vol.12 (8), p.1244-1253

2014

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Biallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunity

Nature communications, 2014-11, Vol.5 (1), p.5360-5360, Article 5360

2014

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Evaluation the oral hygiene conditions, oral Candida colonization and salivary Streptococcus mutans and Lactobacilli density in a group of β-thalassemic children and adolescence

Medicina oral, patología oral y cirugía bucal, 2019-11, Vol.24 (6), p.e712-e718

2019

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L-carnitine deficiency and red blood cell mechanical impairment in beta-thalassemia major

Clinical hemorheology and microcirculation, 2006, Vol.35 (3), p.349

2006

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Efficacy of FEIBA for acute bleeding and surgical haemostasis in haemophilia A patients with inhibitors: a multicentre registry in Turkey

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-05, Vol.18 (3), p.383-391

2012

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Peripheral stem cell transplantation in a child with amegakaryocytic thrombocytopenia

Bone marrow transplantation (Basingstoke), 2000-09, Vol.26 (5), p.571-572

2000

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Two rare mutations in Turkey: IVS I.130(G–C) and IVS II.848(C–A)

Clinical and laboratory haematology, 2005-08, Vol.27 (4), p.274-277

2005

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Successful hematopoietic SCT from non-identical twins to two sisters with [beta]-thalassemia major by using preimplantation genetic diagnosis and HLA typing.(human leucocyte antigen)(Clinical report)

Bone marrow transplantation (Basingstoke), 2011-12, Vol.46 (12), p.1581

2011

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Plasma homocysteine levels in patients with -thalassaemia major

Scandinavian journal of clinical and laboratory investigation, 2008, Vol.68 (2), p.134-139

2008

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Donor lymphocyte infusions after allogeneic bone marrow transplantation for thalassaemia: a single-centre experience

Bone marrow transplantation (Basingstoke), 2009-03, Vol.43 (S1), p.S233

2009

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Successful treatment of Griscelli syndrome with unrelated cord blood transplantation

Bone marrow transplantation (Basingstoke), 2009-03, Vol.43 (S1), p.S186

2009

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High-dose acyclovir and pre-emptive ganciclovir in prevention of cytomegalovirus disease in pediatric patients following peripheral blood stem cell transplantation

Bone marrow transplantation (Basingstoke), 2004-05, Vol.33 (9), p.931-935

2004

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Aberrations of chromosomes 9 and 22 in acute lymphoblastic leukemia cases detected by ES-fluorescence in situ hybridization

Genetic testing and molecular biomarkers, 2012-05, Vol.16 (5), p.318

2012

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Thalassemia major patients using iron chelators showed a reduced plasma thioredoxin level and reduced thioredoxin reductase activity, despite elevated oxidative stress

A Phase 3 Randomized Trial of Voxelotor in Sickle Cell Disease

Alterations of panoramic radiomorphometric indices in children and adolescents with beta-thalassemia major: A fractal analysis study

Establishing a harmonized haemophilia registry for countries with developing health care systems

Safety of dabigatran etexilate for the secondary prevention of venous thromboembolism in children

The value of early treatment in patients with haemophilia and inhibitors

Successful hematopoietic SCT from non-identical twins to two sisters with β-thalassemia major by using preimplantation genetic diagnosis and HLA typing

Prophylaxis vs. on‐demand treatment with BAY 81‐8973, a full‐length plasma protein‐free recombinant factor VIII product: results from a randomized trial (LEOPOLD II)

Chemotherapy for transient myeloproliferative disorder in a premature infant with Down syndrome

Plasma homocysteine levels in patients with β-thalassaemia major

Recombinant factor VIIa analog in the management of hemophilia with inhibitors: results from a multicenter, randomized, controlled trial of vatreptacog alfa

Outcomes of Allogeneic Hematopoietic Stem Cell Transplantation for Congenital Amegakaryocytic Thrombocytopenia, a PDWP/EBMT Study

Biallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunity

Different Kinetics and Risk Factors for Isolated Extramedullary Relapse after Allogeneic Hematopoietic Stem Cell Transplantation in Children with Acute Leukemia

Evaluation the oral hygiene conditions, oral Candida colonization and salivary Streptococcus mutans and Lactobacilli density in a group of β-thalassemic children and adolescence

L-carnitine deficiency and red blood cell mechanical impairment in beta-thalassemia major

Efficacy of FEIBA for acute bleeding and surgical haemostasis in haemophilia A patients with inhibitors: a multicentre registry in Turkey

Peripheral stem cell transplantation in a child with amegakaryocytic thrombocytopenia

Two rare mutations in Turkey: IVS I.130(G–C) and IVS II.848(C–A)

Successful hematopoietic SCT from non-identical twins to two sisters with [beta]-thalassemia major by using preimplantation genetic diagnosis and HLA typing.(human leucocyte antigen)(Clinical report)

Plasma homocysteine levels in patients with -thalassaemia major

Donor lymphocyte infusions after allogeneic bone marrow transplantation for thalassaemia: a single-centre experience

Successful treatment of Griscelli syndrome with unrelated cord blood transplantation

High-dose acyclovir and pre-emptive ganciclovir in prevention of cytomegalovirus disease in pediatric patients following peripheral blood stem cell transplantation

Aberrations of chromosomes 9 and 22 in acute lymphoblastic leukemia cases detected by ES-fluorescence in situ hybridization

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