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Journal Abstract Search

262 related items for PubMed ID: 3332099

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  • 2. [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; 203(4):284-95. PubMed ID: 1942935
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  • 3. 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
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  • 7. Spectrin oligomerization is cooperatively coupled to membrane assembly: a linkage targeted by many hereditary hemolytic anemias?
    Giorgi M, Cianci CD, Gallagher PG, Morrow JS.
    Exp Mol Pathol; 2001 Jun 01; 70(3):215-30. PubMed ID: 11418000
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  • 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 01; 91(2):502-10. PubMed ID: 8547102
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  • 15. Molecular insights into hereditary elliptocytosis and pyropoikilocytosis: NGS uncovers multiple potential candidate genes.
    Shome DK, Das P, Akbar GA, Taha S, Radhi A, Al-Saad K, Helmy R.
    Ann Hematol; 2023 Sep 01; 102(9):2343-2351. PubMed ID: 37400730
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  • 16. Interactions of spectrin in hereditary elliptocytes containing truncated spectrin beta-chains.
    Eber SW, Morris SA, Schröter W, Gratzer WB.
    J Clin Invest; 1988 Feb 01; 81(2):523-30. PubMed ID: 3276733
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