A comparative evaluation of Eosin-5′-maleimide flow cytometry reveals a high diagnostic efficacy for hereditary spherocytosis

Author:

Joshi P.1,Aggarwal A.1,Jamwal M.1,Sachdeva M. U. S.1,Bansal D.2,Malhotra P.3,Sharma P.1,Das R.1

Affiliation:

1. Department of Hematology; Postgraduate Institute of Medical Education and Research; Chandigarh India

2. Department of Pediatrics; Postgraduate Institute of Medical Education and Research; Chandigarh India

3. Department of Internal Medicine; Postgraduate Institute of Medical Education and Research; Chandigarh India

Funder

Department of Biotechnology , Ministry of Science and Technology

Publisher

Wiley

Subject

Biochemistry (medical),Clinical Biochemistry,Hematology,General Medicine

Reference18 articles.

1. Hereditary spherocytosis- defects in proteins that connect the membrane skeleton to the lipid bilayer;Eber;Semin Hematol,2004

2. Red cell membrane disorders;Gallagher;Hematology Am Soc Hematol Educ Program,2005

3. Erythroid membrane protein defects in hereditary spherocytosis. A study of 62 Spanish cases;Ricard;Haematologica,2000

4. The osmotic resistance (fragility) of human red cells;Parpart;J Clin Invest,1947

5. Using the eosin-5-maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis;King;Cytometry B Clin Cytom,2008

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