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Why genetic engineering experts are putting a spotlight on Victoria Gray’s case
Victoria Gray’s life has been transformed by her treatment for sickle cell disease with the gene-editing technique called CRISPR. She’s in London telling her story at a scientific summit.
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Promising results at 1 year follow-up following familial haploidentical (FHI) T-cell depleted (TCD) with CD34 enrich...AlloSCT from HLA-matched MSD has been su...
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Venous thromboembolism in adults screened for sickle cell trait: a population-based cohort study with nested case-co...OBJECTIVE: To determine whether sickle ...
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James F. Casella, MDDr. James Casella is a professor of pedi...
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‘Every time it’s a battle’: In excruciating pain, sickle cell patients are shunted asideAmy Mason had toughed it out for hours o...
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