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A randomized, placebo-controlled trial of arginine therapy for the treatment of children with sickle cell disease hospitalized with vaso-occlusive pain episodes

Haematologica (Roma), 2013-09, Vol.98 (9), p.1375-1382

2013

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Sildenafil therapy in thalassemia patients with Doppler-defined risk of pulmonary hypertension

Haematologica (Roma), 2013-09, Vol.98 (9), p.1359-1367

2013

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Hydroxycarbamide‐induced changes in E/beta thalassemia red blood cells

American journal of hematology, 2008-11, Vol.83 (11), p.842-845

2008

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A pilot study of subcutaneous decitabine in β-thalassemia intermedia

Blood, 2011-09, Vol.118 (10), p.2708-2711

2011

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Combined chelation therapy with deferasirox and deferoxamine in thalassemia

Blood cells, molecules, & diseases, 2013-02, Vol.50 (2), p.99-104

2013

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Favorable outcomes after in utero transfusion in fetuses with alpha thalassemia major: a case series and review of the literature

Prenatal diagnosis, 2016-12, Vol.36 (13), p.1242-1249

2016

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Treatment of classic pantothenate kinase-associated neurodegeneration with deferiprone and intrathecal baclofen

American journal of physical medicine & rehabilitation, 2013-08, Vol.92 (8), p.728-733

2013

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Chelation use and iron burden in North American and British thalassemia patients: a report from the Thalassemia Longitudinal Cohort

Blood, 2012-03, Vol.119 (12), p.2746-2753

2012

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Red cell alloimmunization in a diverse population of transfused patients with thalassaemia

British journal of haematology, 2011-04, Vol.153 (1), p.121-128

2011

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Validation and reliability of a disease‐specific quality of life measure (the TranQol) in adults and children with thalassaemia major

British journal of haematology, 2014-02, Vol.164 (3), p.431-437

2014

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Relationship among chelator adherence, change in chelators, and quality of life in Thalassemia

Quality of life research, 2014-10, Vol.23 (8), p.2277-2288

2014

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Dysregulated arginine metabolism and cardiopulmonary dysfunction in patients with thalassaemia

British journal of haematology, 2015-06, Vol.169 (6), p.887-898

2015

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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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Darbepoetin alfa for the treatment of anaemia in alpha‐ or beta‐ thalassaemia intermedia syndromes

British journal of haematology, 2011-07, Vol.154 (2), p.281-284

2011

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Fertility potential in thalassemia major women: current findings and future diagnostic tools

Annals of the New York Academy of Sciences, 2010-08, Vol.1202 (1), p.226-230

2010

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Inadequate Dietary Intake in Patients with Thalassemia

Journal of the Academy of Nutrition and Dietetics, 2012-07, Vol.112 (7), p.980-990

2012

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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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Quality of life in thalassemia: A comparison of SF‐36 results from the thalassemia longitudinal cohort to reported literature and the US norms

American journal of hematology, 2011-01, Vol.86 (1), p.92-95

2011

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Elevated tricuspid regurgitant jet velocity in subgroups of thalassemia patients: insight into pathophysiology and the effect of splenectomy

Annals of hematology, 2014-07, Vol.93 (7), p.1139-1148

2014

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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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Fetal haemoglobin augmentation in E/β° thalassaemia : clinical and haematological outcome

British journal of haematology, 2005-11, Vol.131 (3), p.378-388

2005

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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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Pain as an emergent issue in thalassemia

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

2010

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Arginine therapy : a novel strategy to induce nitric oxide production in sickle cell disease

British journal of haematology, 2000-11, Vol.111 (2), p.498-500

2000

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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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A randomized, placebo-controlled trial of arginine therapy for the treatment of children with sickle cell disease hospitalized with vaso-occlusive pain episodes

Sildenafil therapy in thalassemia patients with Doppler-defined risk of pulmonary hypertension

Hydroxycarbamide‐induced changes in E/beta thalassemia red blood cells

A pilot study of subcutaneous decitabine in β-thalassemia intermedia

Combined chelation therapy with deferasirox and deferoxamine in thalassemia

Favorable outcomes after in utero transfusion in fetuses with alpha thalassemia major: a case series and review of the literature

Treatment of classic pantothenate kinase-associated neurodegeneration with deferiprone and intrathecal baclofen

Chelation use and iron burden in North American and British thalassemia patients: a report from the Thalassemia Longitudinal Cohort

Red cell alloimmunization in a diverse population of transfused patients with thalassaemia

Validation and reliability of a disease‐specific quality of life measure (the TranQol) in adults and children with thalassaemia major

Relationship among chelator adherence, change in chelators, and quality of life in Thalassemia

Dysregulated arginine metabolism and cardiopulmonary dysfunction in patients with thalassaemia

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

Darbepoetin alfa for the treatment of anaemia in alpha‐ or beta‐ thalassaemia intermedia syndromes

Fertility potential in thalassemia major women: current findings and future diagnostic tools

Inadequate Dietary Intake in Patients 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

Quality of life in thalassemia: A comparison of SF‐36 results from the thalassemia longitudinal cohort to reported literature and the US norms

Elevated tricuspid regurgitant jet velocity in subgroups of thalassemia patients: insight into pathophysiology and the effect of splenectomy

Increased leucocyte apoptosis in transfused β‐thalassaemia patients

Fetal haemoglobin augmentation in E/β° thalassaemia : clinical and haematological outcome

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

Pain as an emergent issue in thalassemia

Arginine therapy : a novel strategy to induce nitric oxide production in sickle cell disease

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

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