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Journal Abstract Search

222 related items for PubMed ID: 8347735

  • 1.
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  • 2. 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; 15(3):284-8. PubMed ID: 10895969
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  • 4. Red cell membrane protein abnormalities in hereditary spherocytosis in Brazil.
    Saad ST, Costa FF, Vicentim DL, Salles TS, Pranke PH.
    Br J Haematol; 1994 Oct; 88(2):295-9. PubMed ID: 7803273
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  • 5. Splenectomy prolongs in vivo survival of erythrocytes differently in spectrin/ankyrin- and band 3-deficient hereditary spherocytosis.
    Reliene R, Mariani M, Zanella A, Reinhart WH, Ribeiro ML, del Giudice EM, Perrotta S, Iolascon A, Eber S, Lutz HU.
    Blood; 2002 Sep 15; 100(6):2208-15. PubMed ID: 12200387
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  • 6. Search for the candidate genes in dominant hereditary spherocytosis using linkage analysis.
    Garbarz M, Bibas D, Cynober T, Galand C, Bournier O, Devaux I, Tchernia G, Dhermy D.
    C R Acad Sci III; 1996 Oct 15; 319(10):913-9. PubMed ID: 8977772
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  • 8. Ankyrin deficiency in dominant hereditary spherocytosis: report of three cases.
    Iolascon A, Miraglia del Giudice E, Camaschella C, Pinto L, Nobili B, Perrotta S, Cutillo S.
    Br J Haematol; 1991 Aug 15; 78(4):551-4. PubMed ID: 1832935
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  • 10. Regulation of band 3 rotational mobility by ankyrin in intact human red cells.
    Cho MR, Eber SW, Liu SC, Lux SE, Golan DE.
    Biochemistry; 1998 Dec 22; 37(51):17828-35. PubMed ID: 9922149
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  • 11. Molecular basis of spectrin and ankyrin deficiencies in severe hereditary spherocytosis: evidence implicating a primary defect of ankyrin.
    Hanspal M, Yoon SH, Yu H, Hanspal JS, Lambert S, Palek J, Prchal JT.
    Blood; 1991 Jan 01; 77(1):165-73. PubMed ID: 1702027
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  • 14. A genetic defect of erythrocyte band 4.2 protein associated with hereditary spherocytosis.
    Ideguchi H, Nishimura J, Nawata H, Hamasaki N.
    Br J Haematol; 1990 Mar 01; 74(3):347-53. PubMed ID: 2139792
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  • 16. Molecular basis of spectrin deficiency in beta spectrin Durham. A deletion within beta spectrin adjacent to the ankyrin-binding site precludes spectrin attachment to the membrane in hereditary spherocytosis.
    Hassoun H, Vassiliadis JN, Murray J, Yi SJ, Hanspal M, Ware RE, Winter SS, Chiou SS, Palek J.
    J Clin Invest; 1995 Dec 01; 96(6):2623-9. PubMed ID: 8675627
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  • 17. Membrane cation and anion transport activities in erythrocytes of hereditary spherocytosis: effects of different membrane protein defects.
    De Franceschi L, Olivieri O, Miraglia del Giudice E, Perrotta S, Sabato V, Corrocher R, Iolascon A.
    Am J Hematol; 1997 Jul 01; 55(3):121-8. PubMed ID: 9256290
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  • 20. [Erythrocyte membrane and hereditary spherocytosis].
    Ideguchi H.
    Rinsho Byori; 1990 Apr 01; 38(4):360-4. PubMed ID: 2195190
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