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2009 NOV 2 ... A report, 'Heart rate variability in beta-thalassemia patients,' is newly published data in European Journal of Haematology. "Cardiac ...
2009 NOV 1 ... India, "The clinical and hematological response to hydroxyurea was evaluated in beta thalassemia patients in western India with variable clinical severity and correlated with genetic ...
2009 NOV 16 ... as supportive therapy to treat chronic anemias, such as myelodysplastic syndromes, thalassemia, and sickle-cell disease, are at risk of iron accumulation. The clinical consequences of ...
2009 NOV 2 ... genetic diseases that require frequent transfusions, such as sickle cell disease and thalassemia, who may develop antibodies to low-immunogenicity antigens present on donor red blood ...
2009 NOV 1 ... Journal (Association of hepcidin promoter c.-582 A>G variant and iron overload in thalassemia major. Haematologica - the Hematology Journal, 2009;94(9):1293-1296). For ...
2009 NOV 9 ... of bone marrow as a source of stem cells (P = .001), as well as with class II or III of thalassemia as an underlying disease in HSCT recipients (P = .019). Treatment with cyclophosphamide ...
2009 NOV 9 ... investigation results, 'Alpha globin gene numbers: an important modifier of HbE/beta thalassemia,' are detailed in a study published in Hematology. According to a study from New Delhi, ...
2009 NOV 1 ... According to recent research from Thailand, "Beta-thalassemia occurs from the imbalanced globin chain synthesis due to the absence or inadequate ...
2009 NOV 2 ... disease. All 83 patients with the deletional type were double heterozygotes of alpha(0)-thalassemia and alpha(+)-thalassemia. The Southeast Asian type of ...
2009 NOV 16 ... on 63 human leucocyte antigen-matched HSCT performed in 57 children affected by beta thalassemia at very high risk for developing VOD (liver fibrosis, iron overload, hepatitis C virus ...
2009 NOV 2 ... study, the aim was to investigate distribution of HCV genotypes in Iranian patients with thalassemia." "Blood samples were received from 280 multiply transfused patients with ...
2009 NOV 9 ... Investigators publish new data in the report 'Pregnancy in beta-thalassemia trait carriers: an uneventful journey.' According to a study from Greece, ...
2009 NOV 1 ... Probe Amplification was performed revealing an unknown G gamma(A gamma delta beta)(0)-thalassemia defect spanning from the A gamma gene to downstream of the beta-globin gene ...
2009 NOV 1 ... but confer major clinical benefits in patients with sickle cell anemia (SCA) and beta thalassemia, diseases that represent major public health problems. Inter-individual HbF variation is ...
2009 NOV 9 ... Medical Device, Myelodysplastic Syndromes, Myeloma, Oncology, Pharmaceuticals, Thalassemia, Therapy, Transfusion Medicine, Treatment, University of Pavia. This ...
2009 NOV 16 ... test (HRT) and tried to determine its significance. Human blood samples from beta-thalassemia patients and healthy controls were analyzed with HRT, which was carried out on ...