Thalassemia

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  Subject Areas on Research

  • A human gamma globin gene variant binds SP1. 
  • A novel beta-globin mutation, beta Durham-NC [beta 114 Leu-->Pro], produces a dominant thalassemia-like phenotype. 
  • Analysis of globin gene structure in patients with beta thalassemia by restriction endonuclease mapping. 
  • Beta-thalassemia resulting from a single nucleotide substitution in an acceptor splice site. 
  • Bone marrow transplantation for hematologic malignancies: the Stanford experience. 
  • Disparity in the management of iron overload between patients with sickle cell disease and thalassemia who received transfusions. 
  • Eighth Annual International Umbilical Cord Blood Transplantation Symposium, San Francisco, California, June 3-5, 2010. 
  • Genetic polymorphisms associated with priapism in sickle cell disease. 
  • Introduction to a symposium on sickle cell anemia: current results of comprehensive care and the evolving role of bone marrow transplantation. 
  • Laboratory profile of sickle cell disease: a cross-sectional analysis. The Cooperative Study of Sickle Cell Disease. 
  • Long-term complications of bone marrow transplantation. 
  • Longitudinal follow up of elevated pulmonary artery pressures in children with sickle cell disease. 
  • Marrow transplantation for disorders of hematopoiesis. 
  • Marrow transplantation for severe aplastic anemia and thalassemia major. 
  • Marrow transplantation for thalassaemia. 
  • Morbidity and mortality in chronically transfused subjects with thalassemia and sickle cell disease: A report from the multi-center study of iron overload. 
  • Overproduction of alpha chains provides a proton-insensitive component to the bluefish hemoglobin system. 
  • Quality of Life Outcomes in a Pediatric Thalassemia Population in Egypt. 
  • Related umbilical cord blood transplantation in patients with thalassemia and sickle cell disease. 
  • The abnormal surface characteristics of the red blood cell membrane in congenital dyserythropoietic anaemia type II (HEMPAS). 
  • The clinical severity of hemoglobin S/Black (A γδβ)0 -thalassemia. 
  • The conserved dinucleotide AG of the 3' splice site may be recognized twice during in vitro splicing of mammalian mRNA precursors. 
  • Umbilical cord blood transplantation for children with thalassemia and sickle cell disease. 
  • Unrelated and HLA-nonidentical related donor marrow transplantation for thalassemia and leukemia. A combined report from the Seattle Marrow Transplant Team and the International Bone Marrow Transplant Registry.