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PUBMED FOR HANDHELDS

Journal Abstract Search

245 related items for PubMed ID: 6675711

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  • 2. Unchanged binding of 99molybdenum to red cell membrane proteins in hereditary spherocytosis.
    Marík T, Kselíková M, Bíbr B, Brabec V, Lener J.
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1983; 110(1):81-5. PubMed ID: 6192057
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  • 3. Hemolytic anemias associated with deficient or dysfunctional spectrin.
    Lux SE, Pease B, Tomaselli MB, John KM, Bernstein SE.
    Prog Clin Biol Res; 1979; 30():463-9. PubMed ID: 531037
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  • 4. 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
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  • 9. [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 18; 43(2):91-4. PubMed ID: 9245075
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  • 13. Hereditary spherocytosis and related disorders.
    Becker PS, Lux SE.
    Clin Haematol; 1985 Feb 18; 14(1):15-43. PubMed ID: 3886234
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  • 14. [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 18; 38(5):393-7. PubMed ID: 8140503
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  • 17. Interactions of spectrin in hereditary elliptocytes containing truncated spectrin beta-chains.
    Eber SW, Morris SA, Schröter W, Gratzer WB.
    J Clin Invest; 1988 Feb 18; 81(2):523-30. PubMed ID: 3276733
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  • 19. Spectrin and spherocytosis.
    Shohet SB.
    N Engl J Med; 1982 May 13; 306(19):1170-1. PubMed ID: 7070421
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