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Journal Abstract Search

415 related items for PubMed ID: 6192057

  • 21. [Membrane abnormalities of red blood cells in hereditary spherocytosis].
    Matsumoto N.
    Nihon Rinsho; 1978 May; Suppl():1606-7. PubMed ID: 691448
    [No Abstract] [Full Text] [Related]

  • 22. [Alteration of erythrocyte membrane proteins in a family with hereditary spherocytosis].
    Inoue F, Matsuyama R, Yoneyama S.
    Nihon Ketsueki Gakkai Zasshi; 1989 Nov; 52(7):1122-7. PubMed ID: 2618557
    [Abstract] [Full Text] [Related]

  • 23. Hereditary spherocytosis and related disorders.
    Becker PS, Lux SE.
    Clin Haematol; 1985 Feb; 14(1):15-43. PubMed ID: 3886234
    [Abstract] [Full Text] [Related]

  • 24. Deficient red-cell spectrin in severe, recessively inherited spherocytosis.
    Agre P, Orringer EP, Bennett V.
    N Engl J Med; 1982 May 13; 306(19):1155-61. PubMed ID: 7070419
    [No Abstract] [Full Text] [Related]

  • 25. Erythrocyte membrane skeleton abnormalities in hereditary spherocytosis.
    Burke BE, Shotton DM.
    Br J Haematol; 1983 Jun 13; 54(2):173-87. PubMed ID: 6849841
    [Abstract] [Full Text] [Related]

  • 26. [Erythrocyte membrane protein abnormalities in hereditary hemolytic anemias].
    Boivin P, Galand C.
    Nouv Rev Fr Hematol Blood Cells; 1977 Jun 13; 18(1):95-116. PubMed ID: 197487
    [Abstract] [Full Text] [Related]

  • 27. Membrane protein phosphorylation in intact normal and hereditary spherocytic human erythrocytes.
    Nakao M, Fujii Y, Hara Y, Nomura T, Nakao T, Komatsu Y.
    J Biochem; 1980 Aug 13; 88(2):327-35. PubMed ID: 7419497
    [No Abstract] [Full Text] [Related]

  • 28. Identification of the molecular defect in the erythrocyte membrane skeleton of some kindreds with hereditary spherocytosis.
    Goodman SR, Shiffer KA, Casoria LA, Eyster ME.
    Blood; 1982 Sep 13; 60(3):772-84. PubMed ID: 7104494
    [Abstract] [Full Text] [Related]

  • 29. [Measurement of phospholipids in erythrocytes, plasma and platelets in a patient with hereditary spherocytosis].
    César JM, Fernández I, Navarro JL.
    Sangre (Barc); 1989 Aug 13; 34(4):300-2. PubMed ID: 2772783
    [Abstract] [Full Text] [Related]

  • 30. Topological Structures and Membrane Nanostructures of Erythrocytes after Splenectomy in Hereditary Spherocytosis Patients via Atomic Force Microscopy.
    Li Y, Lu L, Li J.
    Cell Biochem Biophys; 2016 Sep 13; 74(3):365-71. PubMed ID: 27557951
    [Abstract] [Full Text] [Related]

  • 31. Update on the clinical spectrum and genetics of red blood cell membrane disorders.
    Gallagher PG.
    Curr Hematol Rep; 2004 Mar 13; 3(2):85-91. PubMed ID: 14965483
    [Abstract] [Full Text] [Related]

  • 32. New insights into function of red cell membrane proteins and their interaction with spectrin-based membrane skeleton.
    Mohandas N, An X.
    Transfus Clin Biol; 2006 Mar 13; 13(1-2):29-30. PubMed ID: 16581279
    [No Abstract] [Full Text] [Related]

  • 33. Defective membrane phosphorylation in red cells of a patient with hereditary spherocytosis.
    Yawata Y, Koresawa S, Yamada O, Shibata S.
    Nihon Ketsueki Gakkai Zasshi; 1975 Jun 13; 38(3):311-4. PubMed ID: 1243224
    [No Abstract] [Full Text] [Related]

  • 34. 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 13; 93(9):1310-7. PubMed ID: 18641031
    [Abstract] [Full Text] [Related]

  • 35. [Erythrocyte membrane and hereditary spherocytosis].
    Ideguchi H.
    Rinsho Byori; 1990 Apr 13; 38(4):360-4. PubMed ID: 2195190
    [Abstract] [Full Text] [Related]

  • 36. Specific molybdenum binding to spectrin subunits.
    Marík T, Kselíková M, Bĭbr B, Lener J.
    Cell Biochem Funct; 1984 Jan 13; 2(1):21-2. PubMed ID: 6467511
    [Abstract] [Full Text] [Related]

  • 37. Endogenous phosphorylation of membrane proteins in normal and in hereditary spherocytosis erythrocytes.
    Moret V, Michielin E, Falezza GC, De Sandre G.
    Clin Chim Acta; 1977 Jun 15; 77(3):359-63. PubMed ID: 872436
    [Abstract] [Full Text] [Related]

  • 38. Partial ankyrin and spectrin deficiency in severe, atypical hereditary spherocytosis.
    Coetzer TL, Lawler J, Liu SC, Prchal JT, Gualtieri RJ, Brain MC, Dacie JV, Palek J.
    N Engl J Med; 1988 Jan 28; 318(4):230-4. PubMed ID: 2961992
    [No Abstract] [Full Text] [Related]

  • 39. Hereditary spherocytosis of man. Defective cytoskeletal interactions in the erythrocyte membrane.
    Sawyer WH, Hill JS, Howlett GJ, Wiley JS.
    Biochem J; 1983 May 01; 211(2):349-56. PubMed ID: 6870835
    [Abstract] [Full Text] [Related]

  • 40. Abnormal degradation of erythrocyte membrane proteins in hereditary spherocytosis.
    Gaczyńska M, Bartosz G, Judkiewicz L, Rosin J.
    Clin Chim Acta; 1987 Sep 15; 168(1):7-11. PubMed ID: 3665105
    [Abstract] [Full Text] [Related]

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