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

252 related items for PubMed ID: 638265

  • 21. [Anomalies in erythrocyte membrane lipids during congenital hemolytic anemia].
    Chap H, Douste-Blazy L.
    Nouv Rev Fr Hematol Blood Cells; 1977; 18(1):139-50. PubMed ID: 408790
    [No Abstract] [Full Text] [Related]

  • 22. Erythrocyte membrane vacuole formation in hereditary spherocytosis.
    Schrier SL, Ben-Bassat I, Bensch K, Seeger M, Junga I.
    Br J Haematol; 1974 Jan; 26(1):59-69. PubMed ID: 4368693
    [No Abstract] [Full Text] [Related]

  • 23. Red cell membrane proteins and lipids in spherocytosis.
    Johnsson R.
    Scand J Haematol; 1978 Apr; 20(4):341-50. PubMed ID: 653313
    [No Abstract] [Full Text] [Related]

  • 24. Failure to demonstrate red cell membrane protein abnormalities in sickle cell anaemia.
    Ballas SK, Burka ER.
    Br J Haematol; 1980 Dec; 46(4):627-9. PubMed ID: 7437340
    [No Abstract] [Full Text] [Related]

  • 25. [Studies on the protein composition of red-cell membrane in hereditary spherocytosis (author's transl)].
    Mazo E, Fernández J, Zubizarreta A, Rocha E.
    Sangre (Barc); 1979 Dec; 24(4):376-88. PubMed ID: 483115
    [No Abstract] [Full Text] [Related]

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

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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

  • 30. [Hemolytic anemia caused by congenital anomalies of the erythrocyte membrane].
    Boivin P.
    J Genet Hum; 1986 Nov; 34(5):393-412. PubMed ID: 3540209
    [No Abstract] [Full Text] [Related]

  • 31. [Studies on erythrocyte metabolism in various hemolytic anemias: with special reference to pyruvate kinase deficiency].
    Miwa S, Nishina T, Kakehashi Y, Oyama H.
    Nihon Ketsueki Gakkai Zasshi; 1970 Oct; 33(5):501-18. PubMed ID: 4340177
    [No Abstract] [Full Text] [Related]

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

  • 33. Red cell membrane skeletal defects in hereditary and acquired hemolytic anemias.
    Palek J, Lux SE.
    Semin Hematol; 1983 Jul; 20(3):189-224. PubMed ID: 6353590
    [No Abstract] [Full Text] [Related]

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

  • 35. Organizational differences in the membrane proteins of normal and irreversibly sickled erythrocytes.
    Rubin RW, Milikowski C, Wise GE.
    Biochim Biophys Acta; 1980 Jul; 595(1):1-8. PubMed ID: 7349873
    [Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 38. Erythrocyte membrane proteins in an unusual case of congenital dyserythropoietic anaemia type II (CDA II).
    Harlow RW, Lowenthal RM.
    Br J Haematol; 1982 Jan; 50(1):35-41. PubMed ID: 7055536
    [Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. Inherited sialoglycoprotein deficiencies in human erythrocytes of type En[a-].
    Anstee DJ, Barker DM, Judson PA, Tanner MJ.
    Br J Haematol; 1977 Feb; 35(2):309-20. PubMed ID: 857852
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 13.