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255 related items for PubMed ID: 2195190

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

  • 2. Search for the candidate genes in dominant hereditary spherocytosis using linkage analysis.
    Garbarz M, Bibas D, Cynober T, Galand C, Bournier O, Devaux I, Tchernia G, Dhermy D.
    C R Acad Sci III; 1996 Oct; 319(10):913-9. PubMed ID: 8977772
    [Abstract] [Full Text] [Related]

  • 3. [Hereditary spherocytosis: one year study of erythrocyte membrane proteins].
    Tshilolo L, Kagambega F, Sztern B, Vertongen F, Gulbis B.
    Rev Med Brux; 1998 Oct; 19(5 Pt 1):417-23. PubMed ID: 9844481
    [Abstract] [Full Text] [Related]

  • 4. Erythrocyte membrane protein destabilization versus clinical outcome in 160 Portuguese Hereditary Spherocytosis patients.
    Rocha S, Costa E, Rocha-Pereira P, Ferreira F, Cleto E, Barbot J, Quintanilha A, Belo L, Santos-Silva A.
    Br J Haematol; 2010 Jun; 149(5):785-94. PubMed ID: 20346007
    [Abstract] [Full Text] [Related]

  • 5. Uniquely higher incidence of isolated or combined deficiency of band 3 and/or band 4.2 as the pathogenesis of autosomal dominantly inherited hereditary spherocytosis in the Japanese population.
    Inoue T, Kanzaki A, Yawata A, Wada H, Okamoto N, Takahashi M, Sugihara T, Yamada O, Yawata Y.
    Int J Hematol; 1994 Dec; 60(4):227-38. PubMed ID: 7894027
    [Abstract] [Full Text] [Related]

  • 6. Abnormal phosphoenolpyruvate transport in erythrocytes of hereditary spherocytosis.
    Ideguchi H, Hamasaki N, Ikehara Y.
    Acta Biol Med Ger; 1981 Dec; 40(4-5):555-8. PubMed ID: 7315102
    [Abstract] [Full Text] [Related]

  • 7. Hereditary spherocytosis (HS) due to loss of anion exchange transporter.
    Iolascon A, Miraglia del Giudice E, Perrotta S, Pinto L, Fiorelli G, Cappellini DM, Vasseur C, Bursaux E, Cutillo S.
    Haematologica; 1992 Dec; 77(6):450-6. PubMed ID: 1289181
    [Abstract] [Full Text] [Related]

  • 8. Physiologically important secondary modifications of red cell membrane in hereditary spherocytosis-evidence for in vivo oxidation and lipid rafts protein variations.
    Margetis P, Antonelou M, Karababa F, Loutradi A, Margaritis L, Papassideri I.
    Blood Cells Mol Dis; 2007 Dec; 38(3):210-20. PubMed ID: 17208471
    [Abstract] [Full Text] [Related]

  • 9. Membrane cation and anion transport activities in erythrocytes of hereditary spherocytosis: effects of different membrane protein defects.
    De Franceschi L, Olivieri O, Miraglia del Giudice E, Perrotta S, Sabato V, Corrocher R, Iolascon A.
    Am J Hematol; 1997 Jul; 55(3):121-8. PubMed ID: 9256290
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

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

  • 12. Abnormalities of erythrocyte membrane proteins in Korean patients with hereditary spherocytosis.
    Lee YK, Cho HI, Park SS, Lee YJ, Ra E, Chang YH, Hur M, Shin HY, Ahn HS.
    J Korean Med Sci; 2000 Jun; 15(3):284-8. PubMed ID: 10895969
    [Abstract] [Full Text] [Related]

  • 13. Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis.
    Eber SW, Gonzalez JM, Lux ML, Scarpa AL, Tse WT, Dornwell M, Herbers J, Kugler W, Ozcan R, Pekrun A, Gallagher PG, Schröter W, Forget BG, Lux SE.
    Nat Genet; 1996 Jun; 13(2):214-8. PubMed ID: 8640229
    [Abstract] [Full Text] [Related]

  • 14. [Cytoskeleton anomalies in disorders of red cell membrane proteins].
    Kanzaki A, Wada H, Yawata Y.
    Rinsho Ketsueki; 1991 Jun; 32(6):573-9. PubMed ID: 1832469
    [Abstract] [Full Text] [Related]

  • 15. Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8.
    Lux SE, Tse WT, Menninger JC, John KM, Harris P, Shalev O, Chilcote RR, Marchesi SL, Watkins PC, Bennett V.
    Nature; 1990 Jun 21; 345(6277):736-9. PubMed ID: 2141669
    [Abstract] [Full Text] [Related]

  • 16. Role of the interaction between Lu/BCAM and the spectrin-based membrane skeleton in the increased adhesion of hereditary spherocytosis red cells to laminin.
    Gauthier E, El Nemer W, Wautier MP, Renaud O, Tchernia G, Delaunay J, Le Van Kim C, Colin Y.
    Br J Haematol; 2010 Feb 21; 148(3):456-65. PubMed ID: 20092464
    [Abstract] [Full Text] [Related]

  • 17. Inheritance pattern and clinical response to splenectomy as a reflection of erythrocyte spectrin deficiency in hereditary spherocytosis.
    Agre P, Asimos A, Casella JF, McMillan C.
    N Engl J Med; 1986 Dec 18; 315(25):1579-83. PubMed ID: 3785322
    [Abstract] [Full Text] [Related]

  • 18. Hemolytic anemias associated with deficient or dysfunctional spectrin.
    Lux SE, Pease B, Tomaselli MB, John KM, Bernstein SE.
    Prog Clin Biol Res; 1979 Dec 18; 30():463-9. PubMed ID: 531037
    [Abstract] [Full Text] [Related]

  • 19. Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese population.
    Yawata Y, Kanzaki A, Yawata A, Doerfler W, Ozcan R, Eber SW.
    Int J Hematol; 2000 Feb 18; 71(2):118-35. PubMed ID: 10745622
    [Abstract] [Full Text] [Related]

  • 20. Erythrocyte membrane protein defects in hereditary spherocytosis patients in Turkish population.
    Ayhan AC, Yildiz I, Yüzbaşıoğlu S, Celkan T, Apak H, Ozkan A, Karaman S.
    Hematology; 2012 Jul 18; 17(4):232-6. PubMed ID: 22889517
    [Abstract] [Full Text] [Related]

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