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Journal Abstract Search

362 related items for PubMed ID: 8977772

  • 1. 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]

  • 2. Hereditary spherocytosis with spectrin deficiency related to null mutations of the beta-spectrin gene.
    Dhermy D, Galand C, Bournier O, Cynober T, Méchinaud F, Tchemia G, Garbarz M.
    Blood Cells Mol Dis; 1998 Jun; 24(2):251-61. PubMed ID: 9714702
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. 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 Jun; 77(6):450-6. PubMed ID: 1289181
    [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. 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]

  • 7. [Hereditary spherocytosis: one year study of erythrocyte membrane proteins].
    Tshilolo L, Kagambega F, Sztern B, Vertongen F, Gulbis B.
    Rev Med Brux; 1998 Oct 21; 19(5 Pt 1):417-23. PubMed ID: 9844481
    [Abstract] [Full Text] [Related]

  • 8. [Erythrocyte membrane and hereditary spherocytosis].
    Ideguchi H.
    Rinsho Byori; 1990 Apr 21; 38(4):360-4. PubMed ID: 2195190
    [Abstract] [Full Text] [Related]

  • 9. Hereditary spherocytosis: identification of several HS families with ankyrin and band 3 deficiency in a population of southwestern Poland.
    Bogusławska DM, Heger E, Chorzalska A, Nierzwicka M, Hołojda J, Swiderska A, Straburzyńska A, Paździor G, Langner M, Sikorski AF.
    Ann Hematol; 2004 Jan 21; 83(1):28-33. PubMed ID: 14517693
    [Abstract] [Full Text] [Related]

  • 10. Spectrin oligomerization is cooperatively coupled to membrane assembly: a linkage targeted by many hereditary hemolytic anemias?
    Giorgi M, Cianci CD, Gallagher PG, Morrow JS.
    Exp Mol Pathol; 2001 Jun 21; 70(3):215-30. PubMed ID: 11418000
    [Abstract] [Full Text] [Related]

  • 11. 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 21; 149(5):785-94. PubMed ID: 20346007
    [Abstract] [Full Text] [Related]

  • 12. 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 21; 71(2):118-35. PubMed ID: 10745622
    [Abstract] [Full Text] [Related]

  • 13. [Molecular mechanism of hereditary spherocytosis].
    Bogusławska DM, Heger E, Sikorski AF.
    Pol Merkur Lekarski; 2006 Jan 21; 20(115):112-6. PubMed ID: 16617750
    [Abstract] [Full Text] [Related]

  • 14. Combined spectrin and ankyrin deficiency is common in autosomal dominant hereditary spherocytosis.
    Savvides P, Shalev O, John KM, Lux SE.
    Blood; 1993 Nov 15; 82(10):2953-60. PubMed ID: 8219186
    [Abstract] [Full Text] [Related]

  • 15. Linkage of dominant hereditary spherocytosis to the gene for the erythrocyte membrane-skeleton protein ankyrin.
    Costa FF, Agre P, Watkins PC, Winkelmann JC, Tang TK, John KM, Lux SE, Forget BG.
    N Engl J Med; 1990 Oct 11; 323(15):1046-50. PubMed ID: 1977081
    [No Abstract] [Full Text] [Related]

  • 16. Ankyrin deficiency in dominant hereditary spherocytosis: report of three cases.
    Iolascon A, Miraglia del Giudice E, Camaschella C, Pinto L, Nobili B, Perrotta S, Cutillo S.
    Br J Haematol; 1991 Aug 11; 78(4):551-4. PubMed ID: 1832935
    [Abstract] [Full Text] [Related]

  • 17. Characterization of the underlying molecular defect in hereditary spherocytosis associated with spectrin deficiency.
    Hassoun H, Vassiliadis JN, Murray J, Njolstad PR, Rogus JJ, Ballas SK, Schaffer F, Jarolim P, Brabec V, Palek J.
    Blood; 1997 Jul 01; 90(1):398-406. PubMed ID: 9207476
    [Abstract] [Full Text] [Related]

  • 18. 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 01; 15(3):284-8. PubMed ID: 10895969
    [Abstract] [Full Text] [Related]

  • 19. 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 01; 93(9):1310-7. PubMed ID: 18641031
    [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 01; 17(4):232-6. PubMed ID: 22889517
    [Abstract] [Full Text] [Related]

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