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

  • 21. Hemolytic anemias due to abnormalities in red cell spectrin: a brief review.
    Lux SE, Wolfe LC, Pease B, Tomaselli MB, John KM, Bernstein SE.
    Prog Clin Biol Res; 1981; 45():159-68. PubMed ID: 7017750
    [No Abstract] [Full Text] [Related]

  • 22. Hereditary spherocytosis.
    Bajracharya BL, Giri A, Baral MR.
    Kathmandu Univ Med J (KUMJ); 2004; 2(2):145-8. PubMed ID: 15821383
    [Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25. 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
    [Abstract] [Full Text] [Related]

  • 26. [Current data on the pathogenesis of hereditary spherocytosis (Minkowski-Shauffard's anemia) (review of the literature and personal study)].
    Kovalev IuR, Shabalov NP, Iuzhanina TA, Borisova TZ.
    Probl Gematol Pereliv Krovi; 1970 Oct; 15(10):34-9. PubMed ID: 4255204
    [No Abstract] [Full Text] [Related]

  • 27. [Diagnostic value of acidified glycerol lysis test (AGLT) in hereditary spherocytosis and selected hematologic diseases].
    Apel D, Mariańska B, Maj S.
    Acta Haematol Pol; 1993 Oct; 24(3):267-71. PubMed ID: 8249541
    [Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29. Increased membrane-protein methylation in hereditary spherocytosis. A marker of cytoskeletal disarray.
    Ingrosso D, D'Angelo S, Perna AF, Iolascon A, Miraglia del Giudice E, Perrotta S, Zappia V, Galletti P.
    Eur J Biochem; 1995 Mar 15; 228(3):894-8. PubMed ID: 7737191
    [Abstract] [Full Text] [Related]

  • 30. Experience with measurement of erythrocyte osmotic fragility by a dialysis technique in congenital hereditary spherocytosis.
    Hendley JO, Porter FS.
    J Lab Clin Med; 1969 Feb 15; 73(2):219-28. PubMed ID: 5764018
    [No Abstract] [Full Text] [Related]

  • 31. [Molecular pathology of the erythrocyte membrane].
    Delaunay J.
    Rev Prat; 1993 Jun 01; 43(11):1392-6. PubMed ID: 8235389
    [Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36. 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 01; 74(4):244-50. PubMed ID: 18454487
    [Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39. 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 01; 70(3):215-30. PubMed ID: 11418000
    [Abstract] [Full Text] [Related]

  • 40. [Incubated osmotic fragility test does not exclude red blood cell membrane disorders! About a case of hereditary elliptocytosis].
    Perrin J, Marchand-Arvier M, Latger-Cannard V, Vigneron C, Lecompte T.
    Ann Biol Clin (Paris); 2006 Jun 01; 64(5):491-5. PubMed ID: 17040882
    [Abstract] [Full Text] [Related]

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