Beta Thalassemia Carriers detection empowered federated Learning [PDF]
Muhammad Shoaib Farooq, Hafiz Ali Younas
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Renal tubular dysfunction with nephrocalcinosis in a patient with beta thalassemia minor
Thalassemia is a hereditary anemia resulting from defect in hemoglobin production. Beta thalassemia is due to impaired production of beta globin chains, leading to a relative excess of alpha globin chains.
Prabahar Murugesan +4 more
doaj
Nutritional deficiencies among adults with beta thalassemia major in Vietnam. [PDF]
Hoang TNA +6 more
europepmc +1 more source
Dietary Patterns Among Patients With Beta-Thalassemia Major in Vietnam. [PDF]
Hoang TNA, Quach HL.
europepmc +1 more source
Combination of a triple alpha-globin gene with beta-thalassemia in a gypsy family: importance of the genetic testing in the diagnosis and search for a donor for bone marrow transplantation for one of their children [PDF]
Flor Yus Cebrian +4 more
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Unraveling the link: Beta-thalassemia intermedia and Moyamoya syndrome-a hidden connection. [PDF]
Yap TC, Ismail MI.
europepmc +1 more source
Hematopoietic Stem Cell Transplantation From Unrelated Donor in Children with Beta Thalassemia Major
Gülsün Karasu +7 more
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Lower white matter volume in beta‐thalassemia associated with anemia and cognitive performance [PDF]
Soyoung Choi +2 more
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