Transfusion regimens in thalassemia intermedia
<p>Thalassemia intermedia (TI) is a heterogeneous disease, in terms of both clinical manifestations and underlying molecular defects. Some TI patients are asymptomatic until adult life, whereas others are symptomatic from early childhood. In contrast with patients with Thalassemia major (TM),...
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| Format: | Article |
| Language: | English |
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MDPI AG
2011-12-01
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| Series: | Thalassemia Reports |
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| Online Access: | http://www.pagepressjournals.org/index.php/thal/article/view/304 |