In Utero Transfusions Support Improved Survival in Patients With Alpha Thalassemia Major
Researchers sought to determine whether in utero transfusions would yield improved survival for patients with alpha thalassemia major.
Diagnosis & Disease Information
Hepatocyte Transferrin Receptor 1 Linked With Iron Homeostasis, Showing Implications for Beta-Thalassemia
Researchers sought to determine whether there was a relationship between hepatocyte transferrin receptor 1 and iron homeostasis.
Hydroxyurea Plus Thalidomide Shows Promising Results in Pediatric Patients With Beta-Thalassemia
Researchers sought to determine whether hydroxyurea with thalidomide would improve hemoglobin levels in pediatric patients with beta-thalassemia.
Vitamin D Deficiency Increases Risk of Acute Graft Vs Host Disease in Thalassemia Major
Researchers sought to determine whether vitamin D deficiency before hematopoietic stem cell transplantation would impact risk of GVHD in thalassemia major.
Longitudinal Strain May Help Identify Subclinical Myocardial Dysfunction in Beta-Thalassemia Major
Researchers sought to determine whether longitudinal strain with conventional TTE parameters could identify subclinical myocardial dysfunction associated with iron overload in thalassemia.
Betibeglogene Autotemcel May Improve Quality of Life Among Patients With Beta-Thalassemia
Researchers sought to determine whether treatment with betibeglogene autotemcel could improve QoL in patients with transfusion-dependent beta-thalassemia.
Novel Beta-Thalassemia Deletion Removes Entire Beta-Globin Gene
Researchers investigated a novel beta-thalassemia deletion that removes the entire beta-globin gene.
High Economic Burden Seen for Patients With Thalassemia, Sickle Cell Disease Who Undergo HSCT
Researchers sought to determine the utility of HSCT in patients with beta-thalassemia and SCD with recurrent vaso-occlusive crises.
CMR Evaluation Reveals Predictors of Heart Failure in Thalassemia Major
Researchers sought to determine whether including LGE in CMR-based evaluations of iron-induced heart failure could improve prognostic stratification in thalassemia major.
Mitapivat Associated With Improved Markers of Erythropoietic Activity in Adults With Thalassemia
Researchers sought to determine whether mitapivat would be safe and effective in patients with alpha- or beta-NTDT.
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