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Effectiveness and safety of ICL670 in iron-loaded patients with thalassaemia: a randomised, double-blind, placebo-controlled, dose-escalation trial

The Lancet (British edition), 2003-05, Vol.361 (9369), p.1597-1602

2003

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Safety and pharmacokinetics of the oral iron chelator SP-420 in [beta]-thalassemia

American journal of hematology, 2017-12, Vol.92 (12), p.1356

2017

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Safety and pharmacokinetics of the oral iron chelator SP‐420 in β‐thalassemia

American journal of hematology, 2017-12, Vol.92 (12), p.1356-1361

2017

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Risk factors and mortality associated with an elevated tricuspid regurgitant jet velocity measured by Doppler-echocardiography in thalassemia: a Thalassemia Clinical Research Network report

Blood, 2011-10, Vol.118 (14), p.3794-3802

2011

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Relationship between Chronic Transfusion Therapy and Body Composition in Subjects with Thalassemia

The Journal of pediatrics, 2010-10, Vol.157 (4), p.641-647.e2

2010

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Inflammation and oxidant-stress in β-thalassemia patients treated with iron chelators deferasirox (ICL670) or deferoxamine : an ancillary study of the Novartis CICL670A0107 trial

Haematologica (Roma), 2008-06, Vol.93 (6), p.817-825

2008

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Safety and efficacy of pegylated interferon α-2a and ribavirin for the treatment of hepatitis C in patients with thalassemia

Haematologica (Roma), 2008-08, Vol.93 (8), p.1247-1251

2008

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Relationship between labile plasma iron, liver iron concentration and cardiac response in a deferasirox monotherapy trial

Haematologica (Roma), 2011-07, Vol.96 (7), p.1055-1058

2011

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Chelation therapy in β-thalassemia: An optimistic update

Seminars in hematology, 2001-10, Vol.38 (4), p.360-366

2001

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A preclinical approach for gene therapy of β-thalassemia

Annals of the New York Academy of Sciences, 2010-08, Vol.1202 (1), p.134-140

2010

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Pregnancy outcomes in women with thalassemia in North America and the United Kingdom

American journal of hematology, 2013-09, Vol.88 (9), p.771-773

2013

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Hepcidin and Hfe in iron overload in β-thalassemia

Annals of the New York Academy of Sciences, 2010-08, Vol.1202 (1), p.221-225

2010

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Low Bone Mineral Density in Adolescents with β-Thalassemia

Annals of the New York Academy of Sciences, 2005-11, Vol.1054 (1), p.462-466

2005

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Symptoms of depression and anxiety in patients with thalassemia: Prevalence and correlates in the thalassemia longitudinal cohort

American journal of hematology, 2010-10, Vol.85 (10), p.802-805

2010

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Longitudinal monitoring of cardiac siderosis using cardiovascular magnetic resonance T2 in patients with thalassemia major on various chelation regimens: A 6‐year study

American journal of hematology, 2013-08, Vol.88 (8), p.652-656

2013

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Changes in Bone Microarchitecture and Biomechanical Properties in the th3 Thalassemia Mouse are Associated with Decreased Bone Turnover and Occur During the Period of Bone Accrual

Calcified tissue international, 2010-06, Vol.86 (6), p.484-494

2010

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Increased leucocyte apoptosis in transfused β‐thalassaemia patients

British journal of haematology, 2013-02, Vol.160 (3), p.399-403

2013

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Safety and efficacy of pegylated interferon alpha-2a and ribavirin for the treatment of hepatitis C in patients with thalassemia

Haematologica (Roma), 2008-08, Vol.93 (8), p.1247

2008

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Poster 359 Role of Acute Inpatient Rehabilitation in Spinal Cord Injury due to Extramedullary Hematopoesis in Beta-Thalassemia: A Case Report

PM & R, 2014-09, Vol.6 (9), p.S310-S311

2014

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Pain as an emergent issue in thalassemia

American journal of hematology, 2010-05, Vol.85 (5), p.367-370

2010

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Human T cell lymphotropic virus type 1 infection among U.S. thalassemia patients

AIDS research and human retroviruses, 2013-07, Vol.29 (7), p.1006-1009

2013

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Effect of Transfusional Iron Overload on Immune Response

The Journal of infectious diseases, 2000-09, Vol.182 (Supplement-1), p.S115-S121

2000

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Hemoglobin H‐constant spring in North America: An alpha thalassemia with frequent complications

American journal of hematology, 2009-11, Vol.84 (11), p.759-761

2009

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Education and employment status of children and adults with thalassemia in North America

Pediatric blood & cancer, 2010-10, Vol.55 (4), p.678-683

2010

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Effectiveness and safety of ICL670 in iron-loaded patients with thalassaemia: a randomised, double-blind, placebo-controlled, dose-escalation trial

Safety and pharmacokinetics of the oral iron chelator SP-420 in [beta]-thalassemia

Safety and pharmacokinetics of the oral iron chelator SP‐420 in β‐thalassemia

Risk factors and mortality associated with an elevated tricuspid regurgitant jet velocity measured by Doppler-echocardiography in thalassemia: a Thalassemia Clinical Research Network report

Relationship between Chronic Transfusion Therapy and Body Composition in Subjects with Thalassemia

Inflammation and oxidant-stress in β-thalassemia patients treated with iron chelators deferasirox (ICL670) or deferoxamine : an ancillary study of the Novartis CICL670A0107 trial

Safety and efficacy of pegylated interferon α-2a and ribavirin for the treatment of hepatitis C in patients with thalassemia

Relationship between labile plasma iron, liver iron concentration and cardiac response in a deferasirox monotherapy trial

Chelation therapy in β-thalassemia: An optimistic update

A preclinical approach for gene therapy of β-thalassemia

Pregnancy outcomes in women with thalassemia in North America and the United Kingdom

Hepcidin and Hfe in iron overload in β-thalassemia

Low Bone Mineral Density in Adolescents with β-Thalassemia

Symptoms of depression and anxiety in patients with thalassemia: Prevalence and correlates in the thalassemia longitudinal cohort

Longitudinal monitoring of cardiac siderosis using cardiovascular magnetic resonance T2 in patients with thalassemia major on various chelation regimens: A 6‐year study

Changes in Bone Microarchitecture and Biomechanical Properties in the th3 Thalassemia Mouse are Associated with Decreased Bone Turnover and Occur During the Period of Bone Accrual

Increased leucocyte apoptosis in transfused β‐thalassaemia patients

Safety and efficacy of pegylated interferon alpha-2a and ribavirin for the treatment of hepatitis C in patients with thalassemia

Poster 359 Role of Acute Inpatient Rehabilitation in Spinal Cord Injury due to Extramedullary Hematopoesis in Beta-Thalassemia: A Case Report

Pain as an emergent issue in thalassemia

Human T cell lymphotropic virus type 1 infection among U.S. thalassemia patients

Effect of Transfusional Iron Overload on Immune Response

Hemoglobin H‐constant spring in North America: An alpha thalassemia with frequent complications

Education and employment status of children and adults with thalassemia in North America

Molecular Characterization of 140 Patients in the Pyruvate Kinase Deficiency (PKD) Natural History Study (NHS): Report of 20 New Variants

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