Clinical Hematology and Fundamentals of HemostasisDenise Harmening, Ronald A. Sacher Davis, 1987 - 509 pagina's |
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abnormal acid activity acute addition alpha amount antibody aplastic appear associated beta blood cell body bone marrow cause changes Chapter characteristic chronic clinical cold Color Figure common count cytoplasm decreased defect deficiency described develop diagnosis differential disease disorders drugs effects elevated enzyme erythrocytes examination factors findings function gene globin glucose glycophorin granules Hematology hemoglobin hemolysis hemolytic anemia hereditary immune important increased indicated infections involved iron iron deficiency Laboratory lead less leukemia leukocyte levels liver loss lymphocytes lymphoma major maturation mechanisms megaloblastic membrane mild monocytes morphology neutrophils normal noted occur oxygen patients percent peripheral blood plasma platelet positive present production protein range rare red cell response result reticulocyte seen serum severe smear specific stage stain studies syndrome synthesis Table thalassemia therapy tion tissue transfusion treatment usually vitamin