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A leading study site for nearly a decade, CHOP will be part of a network of treatment centers in the country offering the therapy to patients who require regular blood transfusions.
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Researchers have found a key protein that could become a target for a new treatment for sickle cell disease. In lab tests, blocking the protein reduces sickling that distorts red blood cells.
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Sisters Alyssa and Giuliana Porchia are regular outpatients at CHOP's Alex Scott Day Hospital. Born with beta thalassemia, the girls require monthly blood transfusions.