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Journal Abstract Search

280 related items for PubMed ID: 29338606

  • 1. Utility of mean sphered cell volume and mean reticulocyte volume for the diagnosis of hereditary spherocytosis.
    Arora RD, Dass J, Maydeo S, Arya V, Kotwal J, Bhargava M.
    Hematology; 2018 Aug; 23(7):413-416. PubMed ID: 29338606
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  • 2. Mean reticulocyte volume enhances the utility of red cell mean sphered cell volume in differentiating peripheral blood spherocytes of hereditary spherocytosis from other causes.
    Nair SC, Arora N, Jain S, Inbakumar D, Mammen J, Sitaram U.
    Indian J Pathol Microbiol; 2015 Aug; 58(3):307-9. PubMed ID: 26275251
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  • 4. Mean reticulocyte volume: a specific parameter to screen for hereditary spherocytosis.
    Xu Y, Yang W, Liao L, Deng Z, Qiu Y, Chen W, Lin F.
    Eur J Haematol; 2016 Feb; 96(2):170-4. PubMed ID: 25868528
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  • 6. Automated reticulocyte parameters for hereditary spherocytosis screening.
    Lazarova E, Pradier O, Cotton F, Gulbis B.
    Ann Hematol; 2014 Nov; 93(11):1809-18. PubMed ID: 24912770
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  • 7. Values of mean cell volume and mean sphered cell volume can differentiate hereditary spherocytosis and thalassemia.
    Liao L, Deng ZF, Qiu YL, Chen P, Chen WQ, Lin FQ.
    Hematology; 2014 Oct; 19(7):393-6. PubMed ID: 24620949
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  • 8. 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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  • 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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  • 10. Clinico-hematological profile of hereditary spherocytosis: experience from a tertiary care center in North India.
    Kar R, Rao S, Srinivas UM, Mishra P, Pati HP.
    Hematology; 2009 Jun; 14(3):164-7. PubMed ID: 19490762
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  • 11. Comparison and evaluation of three screening tests of hereditary spherocytosis in Chinese patients.
    Tao YF, Deng ZF, Liao L, Qiu YL, Chen WQ, Lin FQ.
    Ann Hematol; 2015 May; 94(5):747-51. PubMed ID: 25501660
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  • 12. [Flowcytometric diagnostics of hereditary spherocytosis].
    Riley CH, Nikolajsen K, Kjaersgaard E, Klausen TW, Mourits-Andersen T, Clausen N, Lausen B, Rosthøj S, Birgens H.
    Ugeskr Laeger; 2009 Nov 30; 171(49):3610-4. PubMed ID: 19954702
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  • 15. The diagnostic protocol for hereditary spherocytosis-2021 update.
    Wu Y, Liao L, Lin F.
    J Clin Lab Anal; 2021 Dec 30; 35(12):e24034. PubMed ID: 34689357
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  • 18. The GEN.S: a fortuitous finding of a routine screening test for hereditary spherocytosis.
    Chiron M, Cynober T, Mielot F, Tchernia G, Croisille L.
    Hematol Cell Ther; 1999 Jun 30; 41(3):113-6. PubMed ID: 10456441
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  • 19. 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 30; 90(6):625-34. PubMed ID: 21080168
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  • 20. Additional erythrocytic and reticulocytic parameters helpful for diagnosis of hereditary spherocytosis: results of a multicentre study.
    Mullier F, Lainey E, Fenneteau O, Da Costa L, Schillinger F, Bailly N, Cornet Y, Chatelain C, Dogne JM, Chatelain B.
    Ann Hematol; 2011 Jul 30; 90(7):759-68. PubMed ID: 21181161
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