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Journal Abstract Search

235 related items for PubMed ID: 7603093

  • 1. [Abnormal changes in erythrocyte membrane proteins in hereditary spherocytosis and their relation to clinical and biological aspects of the disease].
    Ayala S, Besson I, Aymerich M, Berga L, Vives Corrons JL.
    Med Clin (Barc); 1995 Jun 10; 105(2):45-9. PubMed ID: 7603093
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  • 3. [Relation between types of erythrocyte membrane defects and the clinical picture in hereditary spherocytosis].
    Brabec V, Palek J, Petrtýlová K, Cermák J, Jarolím P.
    Vnitr Lek; 1997 Feb 10; 43(2):91-4. PubMed ID: 9245075
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  • 4. Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect.
    Mariani M, Barcellini W, Vercellati C, Marcello AP, Fermo E, Pedotti P, Boschetti C, Zanella A.
    Haematologica; 2008 Sep 10; 93(9):1310-7. PubMed ID: 18641031
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  • 5. Hereditary spherocytosis (HS) due to loss of anion exchange transporter.
    Iolascon A, Miraglia del Giudice E, Perrotta S, Pinto L, Fiorelli G, Cappellini DM, Vasseur C, Bursaux E, Cutillo S.
    Haematologica; 1992 Sep 10; 77(6):450-6. PubMed ID: 1289181
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  • 6. [Application of 2 electrophoresis techniques to the analysis of erythrocyte membrane proteins in hereditary spherocytosis].
    Ferrándiz F, Ródenas S, Villegas A.
    Sangre (Barc); 1993 Oct 10; 38(5):393-7. PubMed ID: 8140503
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  • 7. Physiologically important secondary modifications of red cell membrane in hereditary spherocytosis-evidence for in vivo oxidation and lipid rafts protein variations.
    Margetis P, Antonelou M, Karababa F, Loutradi A, Margaritis L, Papassideri I.
    Blood Cells Mol Dis; 2007 Oct 10; 38(3):210-20. PubMed ID: 17208471
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  • 8. 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 10; 74(4):244-50. PubMed ID: 18454487
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  • 11. Abnormalities of erythrocyte membrane proteins in Korean patients with hereditary spherocytosis.
    Lee YK, Cho HI, Park SS, Lee YJ, Ra E, Chang YH, Hur M, Shin HY, Ahn HS.
    J Korean Med Sci; 2000 Jun 10; 15(3):284-8. PubMed ID: 10895969
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  • 12. Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) allele.
    Miraglia del Giudice E, Francese M, Polito R, Nobili B, Iolascon A, Perrotta S.
    Haematologica; 1997 Jun 10; 82(3):332-3. PubMed ID: 9234582
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  • 13. Hereditary spherocytosis: identification of several HS families with ankyrin and band 3 deficiency in a population of southwestern Poland.
    Bogusławska DM, Heger E, Chorzalska A, Nierzwicka M, Hołojda J, Swiderska A, Straburzyńska A, Paździor G, Langner M, Sikorski AF.
    Ann Hematol; 2004 Jan 10; 83(1):28-33. PubMed ID: 14517693
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  • 14. [Cytoskeleton anomalies in disorders of red cell membrane proteins].
    Kanzaki A, Wada H, Yawata Y.
    Rinsho Ketsueki; 1991 Jun 10; 32(6):573-9. PubMed ID: 1832469
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  • 17. Protein deficiency balance as a predictor of clinical outcome in hereditary spherocytosis.
    Rocha S, Rebelo I, Costa E, Catarino C, Belo L, Castro EM, Cabeda JM, Barbot J, Quintanilha A, Santos-Silva A.
    Eur J Haematol; 2005 May 10; 74(5):374-80. PubMed ID: 15813910
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  • 19. Hereditary spherocytosis and related disorders.
    Becker PS, Lux SE.
    Clin Haematol; 1985 Feb 10; 14(1):15-43. PubMed ID: 3886234
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  • 20. Erythrocyte membrane protein defects in hereditary spherocytosis patients in Turkish population.
    Ayhan AC, Yildiz I, Yüzbaşıoğlu S, Celkan T, Apak H, Ozkan A, Karaman S.
    Hematology; 2012 Jul 10; 17(4):232-6. PubMed ID: 22889517
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