Encouraging the outcomes of children with beta-thalassaemia major who underwent fresh cord blood transplantation from an HLA-matched sibling donor
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DOI: 10.1080/16078454.2022.2038402
Abstract: ABSTRACT Background Allogeneic haematopoietic stem cell transplantation (allo-HSCT) is currently the only curative treatment for thalassaemia major (TM). Cord blood (CB) from a sibling has different characteristics from marrow and has potential advantages and disadvantages… read more here.
Keywords: thalassaemia major; transplantation; cord blood;
Beta‐thalassaemia major: Prevalence, risk factors and clinical consequences of hypercalciuria
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DOI: 10.1111/bjh.18345
Abstract: Regular transfusion and chelation therapy produces increased life expectancy in thalassaemic patients who may develop new complications. Since few data are available regarding hypercalciuria in β‐thalassaemia major (TM), the aim of our study was to… read more here.
Keywords: thalassaemia major; prevalence risk; prevalence; risk factors ... See more keywords