ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders

Medicine & Life Sciences

• Hereditary Spherocytosis 100%
• Clinical Laboratory Techniques 90%
• Hereditary Elliptocytosis 69%
• Cell Membrane 58%
• Guidelines 51%
• Membrane Proteins 33%
• Monovalent Cations 19%
• Reticulocyte Count 18%
• Lipid Bilayers 15%
• Erythrocyte Membrane 15%
• Splenectomy 14%
• Cations 13%
• Cytoskeleton 13%
• Polyacrylamide Gel Electrophoresis 12%
• Permeability 11%
• Molecular Biology 10%
• Phenotype 8%
• Mutation 7%
• Genes 5%

Chemical Compounds

• Disorder 69%
• Red 55%
• Protein 16%
• Monoatomic Monocation 15%
• SDS Polyacrylamide Gel Electrophoresis 13%
• Mutation 11%
• Permeability 10%
• Lipid 9%
• Chemistry 7%
• Cation 7%