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Journal Abstract Search

153 related items for PubMed ID: 1148392

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  • 2. Hereditary stomatocytosis: association of low 2,3-diphosphoglycerate with increased cation pumping by the red cell.
    Wiley JS, Cooper RA, Adachi K, Asakura T.
    Br J Haematol; 1979 Jan; 41(1):133-41. PubMed ID: 420735
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  • 4. Modification of red cell membrane structure by cholesterol-rich lipid dispersions. A model for the primary spur cell defect.
    Cooper RA, Arner EC, Wiley JS, Shattil SJ.
    J Clin Invest; 1975 Jan; 55(1):115-26. PubMed ID: 162782
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  • 8. Evidence for imbalanced furosemide-sensitive Na+, K+ cotransport in hereditary stomatocytosis.
    Chailley B, Feo C, Garay R, Dagher G, Bruckdorfer R, Fischer S, Piau JP, Delaunay J.
    Scand J Haematol; 1981 Nov; 27(5):365-73. PubMed ID: 7346999
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  • 10. [Hereditary stomatocytosis of the hydrocytosis type: a report of one family and red cell membrane studies].
    Kida T, Nakamura H, Kuroki T, Mizoguchi Y, Kobayashi K, Yamane T, Im T, Tatsumi N, Ata K, Wada H.
    Rinsho Ketsueki; 1990 Jun; 31(6):813-9. PubMed ID: 2170705
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  • 12. Variant type of congenital stomatocytosis.
    Morita H, Wada H, Tsujinoue H, Kurioka T, Ueno Y, Shichikawa K, Amano H, Higo I, Kanzaki A, Yawata Y.
    Intern Med; 1994 Feb; 33(2):103-6. PubMed ID: 8019039
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  • 13. Increased cation permeability in mutant mouse red blood cells with defective membrane skeletons.
    Joiner CH, Franco RS, Jiang M, Franco MS, Barker JE, Lux SE.
    Blood; 1995 Dec 01; 86(11):4307-14. PubMed ID: 7492791
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  • 14. Congenital hemolytic anemia associated with dehydrated erythrocytes and increased potassium loss.
    Glader BE, Fortier N, Albala MM, Nathan DG.
    N Engl J Med; 1974 Sep 05; 291(10):491-6. PubMed ID: 4851153
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  • 17. Correction of the permeability defect in hereditary stomatocytosis by dimethyl adipimidate.
    Mentzer WC, Lubin BH, Emmons S.
    N Engl J Med; 1976 May 27; 294(22):1200-4. PubMed ID: 1264135
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