These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

87 related items for PubMed ID: 3898003

  • 1. [Current theories on the etiopathogenesis of congenital spherocytosis].
    Zelenay E, Ochocka M.
    Pediatr Pol; 1985 Jan; 60(1):91-4. PubMed ID: 3898003
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. Oxidative erythrocyte membrane damage in hereditary spherocytosis.
    Caprari P, Bozzi A, Ferroni L, Strom R, Salvati AM.
    Biochem Int; 1992 Feb; 26(2):265-74. PubMed ID: 1558539
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. [Relation between types of erythrocyte membrane defects and the clinical picture in hereditary spherocytosis].
    Brabec V, Palek J, Petrtýlová K, Cermák J, Jarolím P.
    Vnitr Lek; 1997 Feb; 43(2):91-4. PubMed ID: 9245075
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. [Hereditary diseases of the human erythrocyte membrane skeleton (author's transl)].
    Boivin P.
    Nouv Presse Med; 1982 Jul 03; 11(31):2347-51. PubMed ID: 7111000
    [Abstract] [Full Text] [Related]

  • 10. [Hereditary spherocytosis: one year study of erythrocyte membrane proteins].
    Tshilolo L, Kagambega F, Sztern B, Vertongen F, Gulbis B.
    Rev Med Brux; 1998 Oct 03; 19(5 Pt 1):417-23. PubMed ID: 9844481
    [Abstract] [Full Text] [Related]

  • 11. Marked reduction of spectrinin hereditary spherocytosis in the common house mouse.
    Greenquist AC, Shohet SB, Bernstein SE.
    Blood; 1978 Jun 03; 51(6):1149-55. PubMed ID: 647119
    [Abstract] [Full Text] [Related]

  • 12. Reductions of erythrocyte membrane viscoelastic coefficients reflect spectrin deficiencies in hereditary spherocytosis.
    Waugh RE, Agre P.
    J Clin Invest; 1988 Jan 03; 81(1):133-41. PubMed ID: 3335631
    [Abstract] [Full Text] [Related]

  • 13. Spectrin and spherocytosis.
    Shohet SB.
    N Engl J Med; 1982 May 13; 306(19):1170-1. PubMed ID: 7070421
    [No Abstract] [Full Text] [Related]

  • 14. Spectrin oligomers of the red cell membrane extracts in hereditary spherocytosis.
    Marík T, Kodícek M, Brabec V.
    Biomed Biochim Acta; 1983 May 13; 42(11-12):S32-7. PubMed ID: 6675711
    [Abstract] [Full Text] [Related]

  • 15. Partial deficiency of erythrocyte spectrin in hereditary spherocytosis.
    Agre P, Casella JF, Zinkham WH, McMillan C, Bennett V.
    Nature; 1983 May 13; 314(6009):380-3. PubMed ID: 3982506
    [Abstract] [Full Text] [Related]

  • 16. [Abnormal changes in erythrocyte membrane proteins in hereditary spherocytosis and their relation to clinical and biological aspects of the disease].
    Ayala S, Besson I, Aymerich M, Berga L, Vives Corrons JL.
    Med Clin (Barc); 1995 Jun 10; 105(2):45-9. PubMed ID: 7603093
    [Abstract] [Full Text] [Related]

  • 17. Decreased membrane mechanical stability and in vivo loss of surface area reflect spectrin deficiencies in hereditary spherocytosis.
    Chasis JA, Agre P, Mohandas N.
    J Clin Invest; 1988 Aug 10; 82(2):617-23. PubMed ID: 3403720
    [Abstract] [Full Text] [Related]

  • 18. Recent advances in the understanding of the erythrocyte membrane.
    Lam SK, Quah TC.
    J Singapore Paediatr Soc; 1991 Aug 10; 33(3-4):140-8. PubMed ID: 1812330
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Ankyrins: structure and function in normal cells and hereditary spherocytes.
    Peters LL, Lux SE.
    Semin Hematol; 1993 Apr 10; 30(2):85-118. PubMed ID: 8480190
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 5.