β-Thalassaemias: Highlights from the European Hematology Association Scientific Working Group (EHA-SWG) Scientific Meeting on Anaemias: Diagnosis and Treatment in the Omics Era-Reference-Cited by-同舟云学术

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β-Thalassaemias: Highlights from the European Hematology Association Scientific Working Group (EHA-SWG) Scientific Meeting on Anaemias: Diagnosis and Treatment in the Omics Era

Published:2017-09-22 Issue: Volume: Page:2-10
ISSN:2053-6631
Container-title:EMJ Hematology
language:
Short-container-title:EMJ Hematol

Author:

Weatherall Kate¹

Affiliation:

1. ApotheCom, London, UK

Publisher

European Medical Group

Subject

General Medicine

Reference62 articles.

1. Galanello R et al. Beta-thalassemia. Orphanet J Rare Dis. 2010;5:11.

2. Taher AT et al. Optimal management of beta thalassaemia intermedia. Br J Haematol. 2011;152(5):512-23.

3. Muncie HL Jr, Campbell J. Alpha and beta thalassemia. Am Fam Physician. 2009;80(4):339-44.

4. Vichinsky E. Hemoglobin e syndromes. Hematology Am Soc Hematol Educ Program. 2007:79-83.

5. Musallam KM et al. Non-transfusion-dependent thalassemias. Haematologica. 2013;98(6):833-44.

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