References
- Bolton-Maggs PH, Langer JC, Iolascon A, et al. General haematology task force of the British committee for standards in H. Guidelines for the diagnosis and management of hereditary spherocytosis--2011 update. Br J Haematol. 2012;156:37–49. doi: 10.1111/j.1365-2141.2011.08921.x
- King MJ, Zanella A. Hereditary red cell membrane disorders and laboratory diagnostic testing. Int J Lab Hematol. 2013;35:237–243. doi: 10.1111/ijlh.12070
- Warang P, Gupta M, Kedar P, et al. Flow cytometric osmotic fragility – an effective screening approach for red cell membranopathies. Cytometry B Clin Cytom. 2011;80:186–190. doi: 10.1002/cyto.b.20583
- Nair A, Jain S, Inbakumar D, et al. Mean reticulocyte volume enhances the utility of red cell mean sphered cell volume in differentiating peripheral blood spherocytes of hereditary spherocytosis from other causes. Indian J Pathol Microbiol. 2015;58:307–309. doi: 10.4103/0377-4929.162836
- Da Costa L, Mohandas N, Sorette M, et al. Temporal differences in membrane loss lead to distinct reticulocyte features in hereditary spherocytosis and in immune hemolytic anemia. Blood. 2001;98:2894–2899. doi: 10.1182/blood.V98.10.2894
- Broseus J, Visomblain B, Guy J, et al. Evaluation of mean sphered corpuscular volume for predicting hereditary spherocytosis. Int J Lab Hematol. 2010;32:519–523. doi: 10.1111/j.1751-553X.2009.01216.x
- Roper D, Layton M. Investigation of the hereditary hemolytic anemias: membrane and enzyme abnormalities. 11th ed. In: Bain BJ LM BI, Lewis SM, editors. Philadelphia, PA: Churchill Livingstone Elsevier; 2012. p. 245–254.
- King MJ, Behrens J, Rogers C, et al. Rapid flow cytometric test for the diagnosis of membrane cytoskeleton-associated haemolytic anaemia. Br J Haematol. 2000;111:924–933.
- Hunt L, Greenwood D, Heimpel H, et al. Towards the harmonization of result presentation for the eosin-5’- maleimide (EMA) binding test in the diagnosis of hereditary spherocytosis. Cytometry B Clin Cytom. 2014;88:50–57. doi: 10.1002/cytob.21187
- Won DI, Suh JS. Flow cytometric detection of erythrocyte osmotic fragility. Cytometry B Clin Cytom. 2009;76B:135–141. doi: 10.1002/cyto.b.20448
- Tao YF, Deng ZF, Liao L, et al. Comparison and evaluation of three screening tests of hereditary spherocytosis in Chinese patients. Ann Hematol. 2015;94:747–751. doi: 10.1007/s00277-014-2270-2
- Michalis LA, Cohen AR, Zhao H, et al. Screening for hereditary spherocytosis by use of automated erythrocyte indexes. J Pediatr. 1997;130:957–960. doi: 10.1016/S0022-3476(97)70283-X
- Eberle SE, Sciuccati G, Bonduel M, et al. Erythrocyte indexes in hereditary spherocytosis. Medicina (B Aires). 2007;67:698–700.
- Mariani M, Barcellini W, Vercellati C, et al. Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect. Haematologica. 2008;93:1310–1317. doi: 10.3324/haematol.12546