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Pubmed for Handhelds

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Journal Abstract Search

278 related items for PubMed ID: 2364170

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  • 4. Immunocytochemical study of membrane skeletons in abnormally shaped erythrocytes as revealed by a quick-freezing and deep-etching method.
    Ohno S, Terada N, Fujii Y, Ueda H, Kuramoto H, Kamisawa N.
    Virchows Arch A Pathol Anat Histopathol; 1993; 422(1):73-80. PubMed ID: 7679852
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  • 7. Experience with eosin-5'-maleimide as a diagnostic tool for red cell membrane cytoskeleton disorders.
    Kedar PS, Colah RB, Kulkarni S, Ghosh K, Mohanty D.
    Clin Lab Haematol; 2003 Dec; 25(6):373-6. PubMed ID: 14641141
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  • 8. Partial spectrin deficiency in hereditary pyropoikilocytosis.
    Coetzer TL, Palek J.
    Blood; 1986 Apr; 67(4):919-24. PubMed ID: 3955236
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  • 15. Elliptical erythrocyte membrane skeletons and heat-sensitive spectrin in hereditary elliptocytosis.
    Tomaselli MB, John KM, Lux SE.
    Proc Natl Acad Sci U S A; 1981 Mar; 78(3):1911-5. PubMed ID: 6940197
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  • 17. 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; 74(4):244-50. PubMed ID: 18454487
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  • 18. [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 Jul; 203(4):284-95. PubMed ID: 1942935
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  • 19. Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders.
    Da Costa L, Galimand J, Fenneteau O, Mohandas N.
    Blood Rev; 2013 Jul; 27(4):167-78. PubMed ID: 23664421
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