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Hemoglobin
international journal for hemoglobin research
Volume 34, 2010 - Issue 4
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Erythrocytosis Due to a Combination of the High Oxygen Affinity Hemoglobin Variant, Hb Olympia [β20(B2)Val→Met] with β- and α-Thalassemia Mutations: First Case in the Literature

Vassiliki Kalotychou First Department of Internal Medicine, University of Athens School of Medicine, Laikon Hospital, Athens, GreeceCorrespondence[email protected]
,
Revekka Tzanetea First Department of Internal Medicine, University of Athens School of Medicine, Laikon Hospital, Athens, Greece
,
Kostas Konstantopoulos First Department of Internal Medicine, University of Athens School of Medicine, Laikon Hospital, Athens, Greece
,
Ioannis Papassotiriou Department of Clinical Biochemistry, Aghia Sophia Children's Hospital, Athens, Greece
&
Ioannis Rombos First Department of Internal Medicine, University of Athens School of Medicine, Laikon Hospital, Athens, Greece
Pages 383-388 | Received 30 Nov 2009, Accepted 29 Jan 2010, Published online: 19 Jul 2010

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Amelia Oliveira, Dana Warcel, Nancy Huntley, Perla Eleftheriou & John B. Porter. (2016) Symptomatic Erythrocytosis Due to Homozygosity for Hb Luton [HBA2: c.269A>T (or HBA1)] and α-Thalassemia: A Clinical Update. Hemoglobin 40:2, pages 127-129.
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Mohammed Shakil Akhtar, Fuad Qaw, J. Francis Borgio, Waleed Albuali, Ahmed Suliman, Zaki Nasserullah, Sana Al-Jarrash & Amein Al-Ali. (2013) Spectrum of α-Thalassemia Mutations in Transfusion-Dependent β-Thalassemia Patients from the Eastern Province of Saudi Arabia. Hemoglobin 37:1, pages 65-73.
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Articles from other publishers (1)

Epifania Rita Testa, Adriana Masotti, Patrizia Valeri, Luciana Geremia, Valeria Brunetta & Andrea Bontadini. (2022) Unusual finding of high oxygen affinity haemoglobinopathy treated with phlebotomy: A rare but predictable union. Transfusion and Apheresis Science 61:1, pages 103290.
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