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274 related items for PubMed ID: 3982506

  • 1. Partial deficiency of erythrocyte spectrin in hereditary spherocytosis.
    Agre P, Casella JF, Zinkham WH, McMillan C, Bennett V.
    Nature; ; 314(6009):380-3. PubMed ID: 3982506
    [Abstract] [Full Text] [Related]

  • 2. Inheritance pattern and clinical response to splenectomy as a reflection of erythrocyte spectrin deficiency in hereditary spherocytosis.
    Agre P, Asimos A, Casella JF, McMillan C.
    N Engl J Med; 1986 Dec 18; 315(25):1579-83. PubMed ID: 3785322
    [Abstract] [Full Text] [Related]

  • 3. [Disorders of the membrane skeleton of erythrocytes in hereditary spherocytosis and elliptocytosis: significance of the molecular defect for pathogenesis and clinical severity].
    Eber SW.
    Klin Padiatr; 1991 Dec 18; 203(4):284-95. PubMed ID: 1942935
    [Abstract] [Full Text] [Related]

  • 4. Alteration of the erythrocyte membrane skeletal ultrastructure in hereditary spherocytosis, hereditary elliptocytosis, and pyropoikilocytosis.
    Liu SC, Derick LH, Agre P, Palek J.
    Blood; 1990 Jul 01; 76(1):198-205. PubMed ID: 2364170
    [Abstract] [Full Text] [Related]

  • 5. Deficient red-cell spectrin in severe, recessively inherited spherocytosis.
    Agre P, Orringer EP, Bennett V.
    N Engl J Med; 1982 May 13; 306(19):1155-61. PubMed ID: 7070419
    [No Abstract] [Full Text] [Related]

  • 6. [Erythrocyte membrane and hereditary spherocytosis].
    Ideguchi H.
    Rinsho Byori; 1990 Apr 13; 38(4):360-4. PubMed ID: 2195190
    [Abstract] [Full Text] [Related]

  • 7. Identification of the molecular defect in the erythrocyte membrane skeleton of some kindreds with hereditary spherocytosis.
    Goodman SR, Shiffer KA, Casoria LA, Eyster ME.
    Blood; 1982 Sep 13; 60(3):772-84. PubMed ID: 7104494
    [Abstract] [Full Text] [Related]

  • 8. Beta spectrin PRAGUE: a truncated beta spectrin producing spectrin deficiency, defective spectrin heterodimer self-association and a phenotype of spherocytic elliptocytosis.
    Jarolim P, Wichterle H, Hanspal M, Murray J, Rubin HL, Palek J.
    Br J Haematol; 1995 Oct 13; 91(2):502-10. PubMed ID: 8547102
    [Abstract] [Full Text] [Related]

  • 9. [Determination of spectrin in erythrocytes: an important aid in the diagnosis of hereditary spherocytosis].
    van Zwieten R, Bolscher BG, Schouten-van Meeteren AY, Hoffmann JJ, Roos D.
    Ned Tijdschr Geneeskd; 1995 Nov 04; 139(44):2256-61. PubMed ID: 7501052
    [Abstract] [Full Text] [Related]

  • 10. 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 04; 319(10):913-9. PubMed ID: 8977772
    [Abstract] [Full Text] [Related]

  • 11. Hereditary spherocytosis with spectrin deficiency due to an unstable truncated beta spectrin.
    Hassoun H, Vassiliadis JN, Murray J, Yi SJ, Hanspal M, Johnson CA, Palek J.
    Blood; 1996 Mar 15; 87(6):2538-45. PubMed ID: 8630421
    [Abstract] [Full Text] [Related]

  • 12. 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
    [Abstract] [Full Text] [Related]

  • 13. Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8.
    Lux SE, Tse WT, Menninger JC, John KM, Harris P, Shalev O, Chilcote RR, Marchesi SL, Watkins PC, Bennett V.
    Nature; 1990 Jun 21; 345(6277):736-9. PubMed ID: 2141669
    [Abstract] [Full Text] [Related]

  • 14. Reductions of erythrocyte membrane viscoelastic coefficients reflect spectrin deficiencies in hereditary spherocytosis.
    Waugh RE, Agre P.
    J Clin Invest; 1988 Jan 21; 81(1):133-41. PubMed ID: 3335631
    [Abstract] [Full Text] [Related]

  • 15. [Hereditary spherocytosis: one year study of erythrocyte membrane proteins].
    Tshilolo L, Kagambega F, Sztern B, Vertongen F, Gulbis B.
    Rev Med Brux; 1998 Oct 21; 19(5 Pt 1):417-23. PubMed ID: 9844481
    [Abstract] [Full Text] [Related]

  • 16. Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis.
    Miraglia del Giudice E, Iolascon A, Pinto L, Nobili B, Perrotta S.
    Br J Haematol; 1994 Sep 21; 88(1):52-5. PubMed ID: 7803256
    [Abstract] [Full Text] [Related]

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  • 18. Lipid loss in spectrin deficient mouse erythrocytes.
    Shohet SB.
    Prog Clin Biol Res; 1979 Sep 21; 30():471-4. PubMed ID: 531038
    [No Abstract] [Full Text] [Related]

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