Flow Cytometric Eosin-5′-Maleimide Test is a Sensitive Screen for Hereditary Spherocytosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
http://link.springer.com/article/10.1007/s12288-017-0907-8/fulltext.html
Reference14 articles.
1. McKenzie SB, Lynne Williams J (2010) Clinical laboratory hematology, Third edn, chap 17, pp 320–323
2. Park SH et al (2014) Comparison study of the eosin-5′-maleimide binding test, flow cytometric osmotic fragility test, and cryohemolysis test in the diagnosis of hereditary spherocytosis. Am J Clin Pathol 142(4):474–484
3. Hunt Linda et al (2015) Toward the harmonization of result presentation for the eosin-50′-maleimide binding test in the diagnosis of hereditary spherocytosis. Cytom Part B (Clin Cytom) 88B:50–57
4. Mariani M, Barcellini W, Vercellati C et al (2008) Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect. Haematologica 93:1310–1317
5. D’Alcamo E, Agrigento V, Sclafani S et al (2011) Reliability of EMA binding test in the diagnosis of hereditary spherocytosis in Italian patients. Acta Haematol 125:136–140
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Hereditary spherocytosis: review of cases and discussion of hematologic characteristics and updated diagnostic testing;Journal of Advanced Pediatrics and Child Health;2023-03-13
2. Laboratory Indices in Patients with Positive and Borderline Flow Cytometry Eosin-5-Maleimide-Screening Test Results for Hereditary Spherocytosis;The Journal of Pediatrics;2022-04
3. A Systematic review on diagnostic methods of red cell membrane disorders in Asia;International Journal of Laboratory Hematology;2022-01-23
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