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Changing patterns in the epidemiology of β‐thalassemia

β‐thalassemia major is an inherited hemoglobinopathy that requires lifelong red blood cell transfusions and iron chelation therapy to prevent complications due to iron overload. Traditionally, β‐thalassemia has been more common in certain regions of the world such as the Mediterranean, Middle East,...

詳細記述

保存先:
書誌詳細
出版年:Eur J Haematol
主要な著者: Kattamis, Antonis, Forni, Gian Luca, Aydinok, Yesim, Viprakasit, Vip
フォーマット: Artigo
言語:Inglês
出版事項: John Wiley and Sons Inc. 2020
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC7692954/
https://ncbi.nlm.nih.gov/pubmed/32886826
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/ejh.13512
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