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Feb 1, 2015 ... α-Thalassemia is a microcytic anemia characterized by the downregulation of α-
globin synthesis. Premature destruction of red blood cells in the ...
The authors have described the second case in the United States of chronic
hemolytic anemia resulting from the genetic factors for sicklemia and thalassemia
Two white sisters of Italian parentage in whom thalassemia-hemoglobin C
disease was found, have been presented. This is the third report of such cases
A hemoglobin level of over 10 gm per 100 ml has been maintained by transfusion
in six children with thalassemia major. Chelating agents have been used to ...
Dec 1, 2005 ... Severe thalassemia, based on observations of Italian children with characteristic
anemia and bone deformities, was first described in North ...
Challenges Associated With Prolonged Survival of Patients With Thalassemia:
Transitioning From Childhood to Adulthood. TABLE 1. Thalassemia Pediatric to ...
Thalassemia is a chronic condition that presents a range of clinical and
psychosocial ... Although recent advances in the treatment of thalassemia can