Evaluation of eosin-5-maleimide flow cytometry test in the diagnosis of hereditary spherocytosis
Author:
Affiliation:
1. Department of Haematology and Cell Biology, Faculty of Health Sciences, University of the Free State, South Africa
2. National Health Laboratory Service (NHLS), Universitas Academic Hospital Service Laboratory, South Africa
Publisher
Medpharm Publications
Subject
General Medicine
Reference27 articles.
1. Ma S Deng X Liao L Analysis of the causes of the misdiagnosis of hereditary spherocytosis Oncol Rep 2018 40 3 1451 58 https://doi.org/10.3892/or.2018.6578
2. Coetzer T Erythrocyte membrane disorders Kaushansky K Lichtman MA Prchal JT Williams Haematology 9th New York, NY McGraw Hill Education: McGraw Hill Education 2016 661 88
3. Andolfo I Russo R Gambale A Iolascon A New insights on hereditary erythrocyte membrane defects Haematologica 2016 101 11 1284 94 https://doi.org/10.3324/haematol.2016.142463
4. Gallagher PG Red cells Hematology 2005 13 18 https://doi.org/10.1182/asheducation-2005.1.13
5. Bianchi P Fermo E Vercellati C Diagnostic power of laboratory tests for hereditary spherocytosis: A comparison study in 150 patients grouped according to molecular and clinical characteristics Haematologica 2012 97 4 516 23 https://doi.org/10.1182/asheducation-2005.1.13
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