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Journal Articles

Methemoglobinemia and ascorbate deficiency in hemoglobin E β thalassemia: metabolic and clinical implications

Angela Allen, Christopher Fisher, Anuja Premawardhena, Dayananda Bandara, Ashok Perera, Stephen Allen, Timothy St Pierre, Nancy Olivieri, David Weatherall

Blood (2012) 120 (15): 2939–2944.

https://doi.org/10.1182/blood-2012-06-435875

Published: 2012

Journal Articles

Adaptation to anemia in hemoglobin E-β thalassemia

Angela Allen, Christopher Fisher, Anuja Premawardhena, Timothy Peto, Stephen Allen, Mahinda Arambepola, Vivekanandan Thayalsutha, Nancy Olivieri, David Weatherall

Blood (2010) 116 (24): 5368–5370.

https://doi.org/10.1182/blood-2010-06-289488

Published: 2010

Journal Articles

Serum ferritin level changes in children with sickle cell disease on chronic blood transfusion are nonlinear and are associated with iron load and liver injury

Blood (2009) 114 (21): 4632–4638.

https://doi.org/10.1182/blood-2009-02-203323

Published: 2009

Journal Articles

Vertebral Abnormalities by Spine Morphometry in Thalassemia.

Maria Vogiatzi, Eric Macklin, Robert Schneider, Joseph Lane, Irina Chaikodinov, Nancy Olivieri, Melanie Kirby, Elliott Vichinky, Ellen Fung, Janet Kwiatkowski, Melody Cunningham, Patricia Giardina

Blood (2006) 108 (11): 3829.

https://doi.org/10.1182/blood.V108.11.3829.3829

Published: 2006

Journal Articles

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

Blood (2006) 107 (9): 3455–3462.

https://doi.org/10.1182/blood-2005-08-3430

Published: 2006

Journal Articles

High Prevalence of Fractures and Bone Pain in Thalassemia: The Thalassemia Clinical Research Network Experience.

Maria Vogiatzi, MD, Eric Macklin, PhD, Robert Schneider, MD, Joseph Lane, MD, Nancy Olivieri, MD, Melanie Kirby, MD, Angela Cheung, MD, Elliott Vichinsky, MD, Ellen Fung, PhD, Alan Cohen, MD, Janet Kwiatkowski, MD, Virginia Stallings, MD, Ingrid Holm, MD, Ellis Neufeld, MD, Patricia J. Giardina, MD

Blood (2005) 106 (11): 2706.

https://doi.org/10.1182/blood.V106.11.2706.2706

Published: 2005

Journal Articles

Pregnancy in Thalassemia Patients and Their Partners in a Canadian Population.

Anthony Apostoli, BSc, Amanda Cipolla, Maureen Kinghorn, Jacob Kaufman, Giulia Muraca, Nancy Olivieri, MD

Blood (2005) 106 (11): 3835.

https://doi.org/10.1182/blood.V106.11.3835.3835

Published: 2005

Journal Articles

A Phase II Study with ICL670 (Exjade®), a Once-Daily Oral Iron Chelator, in Patients with Various Transfusion-Dependent Anemias and Iron Overload.

John Porter, MD, Elliot Vichinsky, MD, Christian Rose, MD, Antonio Piga, MD, Nancy Olivieri, MD, Norbert Gattermann, MD, Johan Maertens, MD, Bertrand Rabault, PhD, Insa Gathmann, MSc, Daniele Alberti, MD

Blood (2004) 104 (11): 3193.

https://doi.org/10.1182/blood.V104.11.3193.3193

Published: 2004

Journal Articles

Low Bone Mass in Thalassemia: The Thalassemia Clinical Research Network (TCRN) Experience.

Maria G. Vogiatzi, MD, Joseph Lane, MD, Martin Fleisher, MD, Eric A. Macklin, PhD, Ellen B. Fung, PhD, Melanie Kirby, MD, Janet Kwiatkowski, MD, Ingrid Holm, MD, Nancy Olivieri, MD, Elliott Vichinsky, MD, Patricia J. Giardina, MD

Blood (2004) 104 (11): 3613.

https://doi.org/10.1182/blood.V104.11.3613.3613

Published: 2004

Journal Articles

Progression of Avascular Necrosis of the Hip in Sickle Cell Disease: 2 Year Follow-Up of Randomized Trial of Aggressive Physical Therapy and Hip Coring Decompression.

Blood (2004) 104 (11): 1685.

https://doi.org/10.1182/blood.V104.11.1685.1685

Published: 2004

Journal Articles

Stroke risk in siblings with sickle cell anemia

M. Catherine Driscoll, Anne Hurlet, Lori Styles, Virgil McKie, Beatrice Files, Nancy Olivieri, Charles Pegelow, Brian Berman, Richard Drachtman, Kantilal Patel, Donald Brambilla

Blood (2003) 101 (6): 2401–2404.

https://doi.org/10.1182/blood.V101.6.2401

Published: 2003

NARROW

Methemoglobinemia and ascorbate deficiency in hemoglobin E β thalassemia: metabolic and clinical implications

Adaptation to anemia in hemoglobin E-β thalassemia

Serum ferritin level changes in children with sickle cell disease on chronic blood transfusion are nonlinear and are associated with iron load and liver injury

Vertebral Abnormalities by Spine Morphometry in Thalassemia.

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

High Prevalence of Fractures and Bone Pain in Thalassemia: The Thalassemia Clinical Research Network Experience.

Pregnancy in Thalassemia Patients and Their Partners in a Canadian Population.

A Phase II Study with ICL670 (Exjade®), a Once-Daily Oral Iron Chelator, in Patients with Various Transfusion-Dependent Anemias and Iron Overload.

Low Bone Mass in Thalassemia: The Thalassemia Clinical Research Network (TCRN) Experience.

Progression of Avascular Necrosis of the Hip in Sickle Cell Disease: 2 Year Follow-Up of Randomized Trial of Aggressive Physical Therapy and Hip Coring Decompression.

Stroke risk in siblings with sickle cell anemia

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American Society of Hematology

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ASH Publications

American Society of Hematology

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