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PUBMED FOR HANDHELDS

Journal Abstract Search


132 related items for PubMed ID: 29945336

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  • 2. Eosin-5'-maleimide binding test-Do we use appropriate reference values to detect hereditary spherocytosis in neonates?
    Ciepiela O, Nowak M, Wrońska M, Adamowicz-Salach A, Kotuła I.
    Int J Lab Hematol; 2019 Jun; 41(3):e57-e60. PubMed ID: 30548189
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  • 3. 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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  • 4. 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
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  • 5. Early postnatal diagnosis of hereditary spherocytosis by combining light microscopy, acidified glycerol lysis test and eosin-5'-maleimide binding assay.
    Andres O, Eber S, Speer CP.
    Ann Hematol; 2015 Dec; 94(12):1959-64. PubMed ID: 26336967
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  • 9. 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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  • 13. Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among Tunisians.
    Trabelsi N, Bouguerra G, Haddad F, Ouederni M, Darragi I, Boudrigua I, Chaouachi D, Barmat M, Fouzai C, Bejaoui M, Menif S, Kraiem I, Abbes S.
    Cell Physiol Biochem; 2021 Mar 06; 55(1):117-129. PubMed ID: 33667330
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  • 15. Delay in the measurement of eosin-5′-maleimide (EMA) binding does not affect the test result for the diagnosis of hereditary spherocytosis.
    Ciepiela O, Kotuła I, Górska E, Stelmaszczyk-Emmel A, Popko K, Szmydki-Baran A, Adamowicz-Salach A, Demkow U.
    Clin Chem Lab Med; 2013 Apr 06; 51(4):817-23. PubMed ID: 23023797
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  • 16. [Correlation of the degree of band 3 protein absence on erythrocyte membrane by eosin-5'-maleimide binding test and clinical phenotype in hereditary spherocytosis].
    Peng GX, Yang WR, Jing LP, Zhang L, Zhou K, Li Y, Ye L, Li Y, Li JP, Fan HH, Song L, Zhao X, Wu ZJ, Yang Y, Xiong YZ, Wang HJ, Zhang FK.
    Zhonghua Xue Ye Xue Za Zhi; 2017 Jun 14; 38(6):537-541. PubMed ID: 28655100
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  • 17. Evaluating eosin-5-maleimide binding as a diagnostic test for hereditary spherocytosis in newborn infants.
    Christensen RD, Agarwal AM, Nussenzveig RH, Heikal N, Liew MA, Yaish HM.
    J Perinatol; 2015 May 14; 35(5):357-61. PubMed ID: 25357094
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  • 18. 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 14; 38(5):520-6. PubMed ID: 27339613
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