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Articles: Anemia/Polycythemia |
Prior Articles
Treosulfan-based conditioning regimen for allogeneic haematopoietic stem cell transplantation in patients with thalassaemia major
British Journal of Haematology, 10/06/08
Head and neck squamous cell carcinoma in 13 patients with Fanconi anemia after hematopoietic stem cell transplantation
Cancer, 10/06/08 Deferasirox Treatment Improved the Hemoglobin Level and Decreased Transfusion Requirements in Four Patients with the Myelodysplastic Syndrome and Primary Myelofibrosis
Acta Haematologica, 10/01/08 Hydroxycarbamide-induced changes in E/beta thalassemia red blood cells
American Journal of Hematology, 09/30/08 The first case of drug-induced immune hemolytic anemia due to hydrocortisone
Transfusion, 09/30/08 Disparity in the management of iron overload between patients with sickle cell disease and thalassemia who received transfusions
Transfusion, 09/29/08 Iron Supplementation during Treatment with Erythropoiesis-Stimulating Agents for Cancer-Related Anemia
Chemotherapy, 09/29/08 Effects of Aerobic Exercise Training in Anemic Cancer Patients Receiving Darbepoetin Alfa
The Oncologist, 09/29/08 Bone marrow transplantation for severe aplastic anemia secondary to temozolomide
Journal of Neuro-Oncology, 09/29/08 Severe thrombocytopenia and haemolytic anaemia associated with ciprofloxacin: A case report with fatal outcome
Platelets, 09/25/08 Predictors of response to erythropoiesis-stimulating agents (ESA) in cancer patients: the role of baseline serum epoetin level
Clinical and Translational Oncology, 09/23/08 Sheehan's syndrome as a rare cause of anaemia secondary to hypopituitarism
Annals of Hematology, 09/19/08 The effects of air quality on haematological and clinical parameters in children with sickle cell anaemia
Annals of Hematology, 09/16/08 Clinically Significant Differences in the Visual Analog Pain Scale in Acute Vasoocclusive Sickle Cell Crisis
Hemoglobin, 09/16/08 Detection of (beta)-Thalassemia Mutations Using a Multiplex Amplification Refractory Mutation System Assay
Hemoglobin, 09/16/08 Plasma and Urine Hydroxyurea Levels Might be Useful in the Management of Adult Sickle Cell Disease
Hemoglobin, 09/16/08 G6PD deficiency, absence of alpha-thalassemia and hemolytic rate at baseline are significant independent risk factors for abnormally high cerebral velocities in patients with sickle cell anemia
Blood, 09/16/08
Evidence Based Medicine
Existence of cord compression in extramedullary hematopoiesis due to beta thalassemia intermedia
Hematology, 09/15/08 Oxidative process in erythrocytes of individuals with hemoglobin S
Hematology, 09/15/08 Cancer Incidence in Relatives of British Fanconi Anaemia Patients
BMC Cancer, 09/12/08
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Indexed Journals: Journal of Clinical Oncology, Cancer Research, Annals Oncology
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207 Available Pages
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