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Journal Abstract Search

161 related items for PubMed ID: 24243866

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  • 3. Flow cytometric osmotic fragility test and eosin-5'-maleimide dye-binding tests are better than conventional osmotic fragility tests for the diagnosis of hereditary spherocytosis.
    Arora RD, Dass J, Maydeo S, Arya V, Radhakrishnan N, Sachdeva A, Kotwal J, Bhargava M.
    Int J Lab Hematol; 2018 Jun; 40(3):335-342. PubMed ID: 29573337
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  • 5. Percentage of hyperdense cells: Automated parameter to hereditary spherocytosis screening.
    Farias MG, Freitas PA.
    Clin Biochem; 2015 Dec; 48(18):1341-3. PubMed ID: 26210847
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  • 6. Comparison study of the eosin-5'-maleimide binding test, flow cytometric osmotic fragility test, and cryohemolysis test in the diagnosis of hereditary spherocytosis.
    Park SH, Park CJ, Lee BR, Cho YU, Jang S, Kim N, Koh KN, Im HJ, Seo JJ, Park ES, Lee JW, Yoo KH, Jung HL.
    Am J Clin Pathol; 2014 Oct; 142(4):474-84. PubMed ID: 25239414
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  • 8. Evaluation of a Flow-Cytometric Osmotic Fragility Test for Hereditary Spherocytosis in Chinese Patients.
    Tao YF, Deng ZF, Liao L, Qiu YL, Deng XL, Chen WQ, Lin FQ.
    Acta Haematol; 2016 Oct; 135(2):88-93. PubMed ID: 26505491
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  • 9. Flow cytometric detection of erythrocyte osmotic fragility.
    Won DI, Suh JS.
    Cytometry B Clin Cytom; 2009 Mar; 76(2):135-41. PubMed ID: 18727072
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  • 14. [Flow cytometric test using eosin-5'-maleimide (EMA) labelling of red blood for diagnosis of hereditary spherocytosis].
    Wang J, Zheng B, Zhao Y, Chen X, Liu Y, Bo L, Zheng Y, Zhang F, Ru K, Wang H.
    Zhonghua Xue Ye Xue Za Zhi; 2015 Jul; 36(7):598-601. PubMed ID: 26304086
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  • 15. [Osmotic fragility test and RBC shape change analysis using flow cytometry].
    Yamauchi Y, Kayaba H, Itoh W, Ueki S, Moritoki Y, Takeda M, Suzuki T, Itoga M, Hirasawa H, Fujita M, Hihara J.
    Rinsho Byori; 2010 Dec; 58(12):1230-1. PubMed ID: 21417096
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  • 16. Complementary markers for the clinical severity classification of hereditary spherocytosis in unsplenectomized patients.
    Rocha S, Costa E, Rocha-Pereira P, Ferreira F, Cleto E, Barbot J, Quintanilha A, Belo L, Santos-Silva A.
    Blood Cells Mol Dis; 2011 Feb 15; 46(2):166-70. PubMed ID: 21138793
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  • 17. A prospective study to assess the predictive value for hereditary spherocytosis using five laboratory tests (cryohemolysis test, eosin-5'-maleimide flow cytometry, osmotic fragility test, autohemolysis test, and SDS-PAGE) on 50 hereditary spherocytosis families in Argentina.
    Crisp RL, Solari L, Vota D, García E, Miguez G, Chamorro ME, Schvartzman GA, Alfonso G, Gammella D, Caldarola S, Riccheri C, Vittori D, Venegas B, Nesse A, Donato H.
    Ann Hematol; 2011 Jun 15; 90(6):625-34. PubMed ID: 21080168
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  • 19. Screening and confirmation of hereditary spherocytosis in children using a CELL-DYN Sapphire haematology analyser.
    Rooney S, Hoffmann JJ, Cormack OM, McMahon C.
    Int J Lab Hematol; 2015 Feb 15; 37(1):98-104. PubMed ID: 24739214
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