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Journal Abstract Search

187 related items for PubMed ID: 6027083

  • 21.
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  • 22. Correspondence.
    Brodsky I, Reilly CA, Schloss GT.
    Cancer Res; 1971 Oct; 31(10):1513-4. PubMed ID: 5095136
    [No Abstract] [Full Text] [Related]

  • 23. Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect.
    Mariani M, Barcellini W, Vercellati C, Marcello AP, Fermo E, Pedotti P, Boschetti C, Zanella A.
    Haematologica; 2008 Sep; 93(9):1310-7. PubMed ID: 18641031
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  • 27. Red cell life span after splenectomy in hereditary spherocytosis.
    Chapman RG, McDonald LL.
    J Clin Invest; 1968 Oct; 47(10):2263-7. PubMed ID: 5676521
    [Abstract] [Full Text] [Related]

  • 28. Co-ordinated increase of sodium leak and sodium pump in hereditary spherocytosis.
    Wiley JS.
    Br J Haematol; 1972 May; 22(5):529-42. PubMed ID: 4260663
    [No Abstract] [Full Text] [Related]

  • 29. Energy metabolism in uremic red cells: relationship of red cell adenosine triphosphate concentration to extracellular phosphate.
    Lichtman MA, Miller DR, Weed RI.
    Trans Assoc Am Physicians; 1969 May; 82():331-43. PubMed ID: 5375156
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  • 34. Atypical congenital spherocytosis: evidence of abnormal permeability of K+.
    Brain MC, Beilin LJ, Dacie JV.
    Br J Haematol; 1968 Sep; 15(3):323-4. PubMed ID: 5681490
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  • 35. The incorporation of phosphate into ATP associated with ionic gradients across membranes of human red cell ghosts.
    Lant AF, Whittam R.
    J Physiol; 1968 Jul; 197(1):66P-67P. PubMed ID: 5675083
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  • 36. 31P-NMR study on nucleotides and intracellular pH of hereditary spherocytes.
    Kagimoto T, Hayashi F, Yamasaki M, Morino Y, Akasaka K, Kishimoto S.
    Experientia; 1978 Aug 15; 34(8):1092-3. PubMed ID: 29770
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  • 37. Erythroid membrane protein defects in hereditary spherocytosis. A study of 62 Spanish cases.
    Ricard MP, Gilsanz F, Millan I.
    Haematologica; 2000 Sep 15; 85(9):994-5. PubMed ID: 10980645
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  • 38. [Polymorphism analysis of G199A, Ncol in ANK1 and Memphis I in SLC4A1 genes in Mexican healthy individuals and subjects affected with hereditary spherocytosis].
    Camacho-Torres AL, Sánchez-López JY, Mesa-Cornejo VM, Ibarra B, Perea-Díaz FJ.
    Gac Med Mex; 2006 Sep 15; 142(5):435-7. PubMed ID: 17128827
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  • 39.
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