Results 131 to 140 of about 39,247 (186)
Association Between Iron Overload and Glucose Metabolism in Children and Youth with Transfusion-Dependent Beta Thalassemia: The Role of Chelation Therapy. [PDF]
İncefidan İ +3 more
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Host Immunogenetics and Chronic HCV Infection Shape Atopic Risk in Pediatric Beta-Thalassemia: A Genotype-Phenotype Study. [PDF]
Cuppari C +10 more
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From CBC to clarity: Interpretable detection of beta-thalassemia carriers in imbalanced datasets. [PDF]
Chishti S +4 more
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Clinical Image-Vertebral artery beading in a child with Beta Thalassemia major. [PDF]
Chalipat S +4 more
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Beta thalassemia syndromes: New insights.
Dordevic A +4 more
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Beta-thalassemias are a group of hereditary blood disorders characterized by anomalies in the synthesis of the beta chains of hemoglobin resulting in variable phenotypes ranging from severe anemia to clinically asymptomatic individuals. The total annual incidence of symptomatic individuals is estimated at 1 in 100,000 throughout the world and 1 in 10 ...
Renzo Galanello, Antonio Cao
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Beta-thalassemia Intermedia: An Overview
Pediatric Annals, 2008CME Educational Objectives 1. Review the metabolic pathways critical to maintaining red cell membrane integrity. 2. Produce a classification scheme
F. El Rassi +3 more
openaire +3 more sources
Accelerated atherosclerosis in beta-thalassemia
American Journal of Physiology-Heart and Circulatory Physiology, 2023This work definitively shows for the first time that beta-thalassemia leads to accelerated atherosclerosis. We demonstrated that intravascular hemolysis is a prominent feature in beta-thalassemia and the resulting increases in free heme are mechanistically relevant.
Julian Hurtado +8 more
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Gene addition for beta thalassemia
Annals of the New York Academy of Sciences, 2023Abstract Individuals with transfusion‐dependent beta thalassemia require a high burden of care and experience significant morbidity from the underlying disease and its treatment, which negatively impact the quality of life.
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