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

232 related items for PubMed ID: 7070419

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27. Red cell membrane protein abnormalities in hereditary spherocytosis in Brazil.
    Saad ST, Costa FF, Vicentim DL, Salles TS, Pranke PH.
    Br J Haematol; 1994 Oct; 88(2):295-9. PubMed ID: 7803273
    [Abstract] [Full Text] [Related]

  • 28. [Molecular aspects of erythrocyte membrane disorders].
    Saad ST, Costa FF.
    Rev Assoc Med Bras (1992); 1994 Oct; 40(3):216-24. PubMed ID: 7787875
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. 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; 17(4):232-6. PubMed ID: 22889517
    [Abstract] [Full Text] [Related]

  • 31. [Hereditary elliptocytosis caused by a spectrin deficiency (Sp alpha I/46). 1st patient described in Cuba].
    Estrada del Cueto M, García Meneses M, Pérez Díez de los Ríos G, Lagarde Ampudia M.
    Sangre (Barc); 1992 Dec; 37(6):461-3. PubMed ID: 1293798
    [Abstract] [Full Text] [Related]

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

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

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

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

  • 36. 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; 60(3):772-84. PubMed ID: 7104494
    [Abstract] [Full Text] [Related]

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

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

  • 39. 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]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 12.