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Bone Disease in Thalassemia: A Frequent and Still Unresolved Problem

Journal of bone and mineral research, 2009-03, Vol.24 (3), p.543-557

2009

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Differences in the prevalence of growth, endocrine and vitamin D abnormalities among the various thalassaemia syndromes in North America

British journal of haematology, 2009-09, Vol.146 (5), p.546-556

2009

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Renal dysfunction in patients with thalassaemia

British journal of haematology, 2011-04, Vol.153 (1), p.111-117

2011

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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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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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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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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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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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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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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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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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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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Pain as an emergent issue in thalassemia

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

2010

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Safety of Combined Chelation Therapy with Deferasirox and Deferoxamine in Transfusion-Dependent Thalassemia

Blood, 2009-11, Vol.114 (22), p.2021-2021

2009

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Symptoms of Anxiety and Depression Among Teens and Adults in the Thalassemia Longitudinal Cohort Study

Blood, 2009-11, Vol.114 (22), p.555-555

2009

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The Impact of the Child with Thalassemia On the Family: Parental Assessment by Child Health Questionnaire

Blood, 2009-11, Vol.114 (22), p.1371-1371

2009

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Quality of Life in Adolescents and Adults with Thalassemia: A Report of the Thalassemia Longitudinal Cohort

Blood, 2009-11, Vol.114 (22), p.556-556

2009

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Hydroxyurea and sodium phenylbutyrate therapy in thalassemia intermedia

American journal of hematology, 1999-12, Vol.62 (4), p.221-227

1999

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Help your patient meet the challenges of Î² thalassemia major

Nursing (Jenkintown, Pa.), 2004-10, Vol.34 (10), p.32HN1

2004

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Growing up with congenital heart disease: the dilemmas of adolescents and young adults [see comment]

Cardiology in the young, 1998-07, Vol.8 (3), p.303

1998

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Changing outcome of homozygous α-thalassemia : Cautious optimism

Journal of pediatric hematology/oncology, 2000-11, Vol.22 (6), p.539-542

2000

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The dilemmas of parents of adolescents and young adults with congenital heart disease

Heart & lung, 1997-05, Vol.26 (3), p.187-195

1997

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Outreach strategies for Southeast Asian communities: experience, practice, and suggestions for approaching Southeast Asian immigrant and refugee communities to provide thalassemia education and trait testing

Journal of pediatric hematology/oncology, 2000-11, Vol.22 (6), p.588-592

2000

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Bone Disease in Thalassemia: A Frequent and Still Unresolved Problem

Differences in the prevalence of growth, endocrine and vitamin D abnormalities among the various thalassaemia syndromes in North America

Renal dysfunction in patients with thalassaemia

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

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

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

Inadequate Dietary Intake in Patients with Thalassemia

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

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

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

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

Pain as an emergent issue in thalassemia

Safety of Combined Chelation Therapy with Deferasirox and Deferoxamine in Transfusion-Dependent Thalassemia

Symptoms of Anxiety and Depression Among Teens and Adults in the Thalassemia Longitudinal Cohort Study

The Impact of the Child with Thalassemia On the Family: Parental Assessment by Child Health Questionnaire

Quality of Life in Adolescents and Adults with Thalassemia: A Report of the Thalassemia Longitudinal Cohort

Hydroxyurea and sodium phenylbutyrate therapy in thalassemia intermedia

Help your patient meet the challenges of Î² thalassemia major

Growing up with congenital heart disease: the dilemmas of adolescents and young adults [see comment]

Changing outcome of homozygous α-thalassemia : Cautious optimism

The dilemmas of parents of adolescents and young adults with congenital heart disease

Outreach strategies for Southeast Asian communities: experience, practice, and suggestions for approaching Southeast Asian immigrant and refugee communities to provide thalassemia education and trait testing

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