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Updated: Jun 2, 2026

05:23
Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
Splenic infarction in a patient with sickle cell trait and hereditary spherocytosis
Allison C Y Tso1, David R Roper, Chieh L Wong
1St Mary's Hospital, Imperial College Healthcare NHS Trust, Praed Street, London, United Kingdom. allisontso@yahoo.co.uk
American Journal of Hematology
|April 22, 2011
Abstract
No abstract available in PubMed .
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On the other...
Erythrocyte disorders can be broadly categorized into two main types: anemic and polycythemic conditions.
A low oxygen-carrying capacity of the blood due to the loss, lower production, or destruction of erythrocytes is termed anemia. Hemorrhagic anemia, for example, occurs when bleeding from an external wound or internal ulcer reduces erythrocyte counts.
On the other...
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