Anemias & Hypocellular Marrow Disorders Recommendations
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Department of Hematology, Ospedale San Martino, Genova, Italy
Hematology Division, Department of Internal Medicine, University Hospital, Geneva, Switzerland
Molecular and Clinical Hematology Branch, The National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, MD, USA
Hematology Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA
- » Aplastic anemia
- » Auto-immune
- » Bone marrow failure as a result of myelodysplasia and leukemia
- » Bone marrow failure from treatments such as chemotherapy
- » Cold agglutinin disease
- » Consequences and management of bone marrow failure
- » Cytogenetics of myelodysplastic syndromes
- » Enzymes
- » Erythropoiesis
- » Hemoglobin
- » Hereditary bone marrow failure syndromes
- » Iron
- » Megaloblastic
- » Membrane
- » Molecular/general
- » Nutritional anemia
- » Paroxysmal nocturnal hemaglobinopathy
- » Prognostic factors and FAB/WHO classification of myelodysplastic syndromes
- » Sideroblastic anemia
Patients with sickle cell disease (SCD) who present with more pronounced hemolytic anemia are prone to more severe complications of their disease (including stroke and renal damage). Co-inheritance of alpha-thalassemia notably reduces the hemolysis in...
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