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Journal Abstract Search
434 related items for PubMed ID: 19842445
1. Rapid flow cytometric test using eosin-5-maleimide for diagnosis of red blood cell membrane disorders. Tachavanich K, Tanphaichitr VS, Utto W, Viprakasit V. Southeast Asian J Trop Med Public Health; 2009 May; 40(3):570-5. PubMed ID: 19842445 [Abstract] [Full Text] [Related]
2. Using the eosin-5-maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis. King MJ, Telfer P, MacKinnon H, Langabeer L, McMahon C, Darbyshire P, Dhermy D. Cytometry B Clin Cytom; 2008 Jul; 74(4):244-50. PubMed ID: 18454487 [Abstract] [Full Text] [Related]
5. Evaluation of eosin-5-maleimide flow cytometric test in diagnosis of hereditary spherocytosis. Kar R, Mishra P, Pati HP. Int J Lab Hematol; 2010 Feb; 32(1 Pt 2):8-16. PubMed ID: 18782334 [Abstract] [Full Text] [Related]
7. Detection of hereditary pyropoikilocytosis by the eosin-5-maleimide (EMA)-binding test is attributable to a marked reduction in EMA-reactive transmembrane proteins. King MJ, Jepson MA, Guest A, Mushens R. Int J Lab Hematol; 2011 Apr; 33(2):205-11. PubMed ID: 21054813 [Abstract] [Full Text] [Related]
8. A comparative evaluation of Eosin-5'-maleimide flow cytometry reveals a high diagnostic efficacy for hereditary spherocytosis. Joshi P, Aggarwal A, Jamwal M, Sachdeva MU, Bansal D, Malhotra P, Sharma P, Das R. Int J Lab Hematol; 2016 Oct; 38(5):520-6. PubMed ID: 27339613 [Abstract] [Full Text] [Related]
9. Flow cytometry as a diagnostic tool for hereditary spherocytosis. Stoya G, Gruhn B, Vogelsang H, Baumann E, Linss W. Acta Haematol; 2006 Oct; 116(3):186-91. PubMed ID: 17016037 [Abstract] [Full Text] [Related]
16. Hereditary spherocytosis diagnosed with the eosin-5'-maleimide binding test. Watanabe T, Ono H, Tajima I, Ishigaki H, Hakamata A, Shirai M, Endoh A, Hongo T. Pediatr Int; 2014 Jun; 56(3):427-9. PubMed ID: 24894931 [Abstract] [Full Text] [Related]
17. Usefulness of the eosin-5'-maleimide cytometric method as a first-line screening test for the diagnosis of hereditary spherocytosis: comparison with ektacytometry and protein electrophoresis. Girodon F, Garçon L, Bergoin E, Largier M, Delaunay J, Fénéant-Thibault M, Maynadié M, Couillaud G, Moreira S, Cynober T. Br J Haematol; 2008 Feb; 140(4):468-70. PubMed ID: 18162119 [No Abstract] [Full Text] [Related]
18. Evaluation of red cell membrane cytoskeletal disorders using a flow cytometric method in South iran. Golafshan HA, Ranjbaran R, Kalantari T, Moezzi L, Karimi M, Behzad-Behbahani A, Aboualizadeh F, Sharifzadeh S. Turk J Haematol; 2014 Mar; 31(1):25-31. PubMed ID: 24764726 [Abstract] [Full Text] [Related]