Your Article Summary
Diamond-Blackfan anemia, a disease of the ribosome
Hematologie, 05/06/09
Da Costa L et al. - Diamond-Blackfan anemia (DBA) is a rare congenital erythroblastopenia with, in 40% of DBA cases, growth retardation and various malformations, mostly in the cephalic area and in the extremities. In 1997, a 7 year-old DBA girl, from Sweden, carried a balanced translocation 46, XX, t(X\;19). She was at the origin of DBA genetic story and led to the discovery of the first gene involved in DBA, the ribosomal protein S19 gene (RPS19).
Related Articles
Diamond Blackfan anemia 2008-2009: broadening the scope of ribosome biogenesis disorders
Current Opinion in Pediatrics, 11/17/09
Relevance Score: 65%
Congenital Disorders of Ribosome Biogenesis
Biology of Blood and Marrow Transplantation, 10/15/09
Relevance Score: 65%
Severe iron overload in Blackfan-Diamond anemia: A case-control study
American Journal of Hematology, 10/09/09
Relevance Score: 65%
Iron-Refractory Iron Deficiency Anemia
Seminars in Hematology, 10/05/09
Relevance Score: 47%
Hereditary Sideroblastic Anemias: Pathophysiology, Diagnosis, and Treatment
Seminars in Hematology, 10/05/09
Relevance Score: 46%
Today in Anemia/Polycythemia...keeping you current
Receive free subspecialty "5-minute updates" via email
Predictors of response to immunosuppressive therapy with antithymocyte globulin and cyclosporine and prognostic factors for survival in patients with severe aplastic anemia
European Journal of Haematology, 12/10/09
Alpha-thalassaemia masked by beta gene defects and a new polyadenylation site mutation on the alpha2-globin gene
European Journal of Haematology, 12/10/09
Arterio-Arterial Anastomoses do not Prevent the Development of Twin Anemia-Polycythemia Sequence
Placenta, 12/10/09

See Latest Articles