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

129 related items for PubMed ID: 4969265

  • 1. Differences between the red cell acetylcholinesterase defects of paroxysmal nocturnal hemoglobinuria and of ABO hemolytic disease.
    Herz F, Kaplan E, Scheye ES.
    Acta Haematol; 1968; 39(2):85-90. PubMed ID: 4969265
    [No Abstract] [Full Text] [Related]

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

  • 3. Red cell acetylcholinesterase deficiency in ABO hemolytic disease of the newborn.
    Herz F, Kaplan E, Scheye ES.
    Clin Chim Acta; 1972 Feb; 36(2):537-42. PubMed ID: 4621511
    [No Abstract] [Full Text] [Related]

  • 4. In vitro modifications of red cell acetylcholinesterase activity.
    Herz F, Kaplan E.
    Br J Haematol; 1974 Feb; 26(2):165-78. PubMed ID: 4602904
    [No Abstract] [Full Text] [Related]

  • 5. Red cell acetylcholinesterase deficiency in autoimmune hemolytic anemia and in paroxysmal nocturnal hemoglobinuria.
    Herz F, Kaplan E, Scheye ES.
    Clin Chim Acta; 1972 May; 38(2):301-6. PubMed ID: 5026353
    [No Abstract] [Full Text] [Related]

  • 6. [Study of the acetylcholinesterase activity of the erythrocytes in hemolytic disease of the newborn].
    Sirchia G, Ferrone S, Milani R, Masera G.
    Haematol Lat; 1966 May; 9(3):215-20. PubMed ID: 4966138
    [No Abstract] [Full Text] [Related]

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

  • 8. [Activity of certain erythrocyte enzymes in hemolytic disease of the newborn].
    Novitskaia AV.
    Vopr Okhr Materin Det; 1976 Jan; 21(1):45-9. PubMed ID: 987642
    [No Abstract] [Full Text] [Related]

  • 9. [Behavior of erythrocytic acetylcholinesterase activity in the hemolytic disease of the newborn due to ABO incompatibility in relation to erythrocyte age].
    Gerlini G, Ottaviano S, Sbraccia C, Carapella E, Bonanni V.
    Riv Clin Pediatr; 1968 Jan; 81(5):742-5. PubMed ID: 5754265
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Red cell acetylcholinesterase in ABO haemolytic disease of the newborn.
    Ferrone S, Zanella A, Sirchia G.
    Experientia; 1968 May 15; 24(5):495. PubMed ID: 4970753
    [No Abstract] [Full Text] [Related]

  • 12. [Acetylcholinesterase in erythrocytes as a criterion for the indication of exchange transfusion in ABO hemolysis of newborn infants].
    Stocker F, Taminelli F, de Muralt G.
    Helv Paediatr Acta; 1969 Oct 15; 24(5):448-57. PubMed ID: 5394098
    [No Abstract] [Full Text] [Related]

  • 13. [Biochemical changes in erythrocytes in iso- and auto-immune hemolytic anemias].
    Kovalev IuR.
    Vopr Med Khim; 1970 Oct 15; 16(5):477-82. PubMed ID: 5002345
    [No Abstract] [Full Text] [Related]

  • 14. Erythrocyte acetylcholinesterase and glucose-6-phosphate dehydrogenase in newborn infants of low birth weight.
    Herz F, Kaplan E, Scheye ES.
    Clin Chim Acta; 1973 Jun 28; 46(2):147-52. PubMed ID: 4745359
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. [Enzymatic and metabolic activities of erythrocytes in paroxysmal nocturnal hemoglobinuria].
    Ferrone S, Zanella A, Sirchia G.
    Acta Vitaminol Enzymol; 1970 Jun 28; 24(6):237-63. PubMed ID: 5537938
    [No Abstract] [Full Text] [Related]

  • 18. The mechanism of decreased red cell acetylcholinesterase activity in patients with paroxysmal nocturnal hemoglobinuria: Its relation to the membrane lipids.
    Shinohara K, Matsumoto N, Ishida Y, Kaneko T.
    Nihon Ketsueki Gakkai Zasshi; 1983 Feb 28; 46(1):25-9. PubMed ID: 6858569
    [No Abstract] [Full Text] [Related]

  • 19. [Determination of glucose-6-phosphate dehydrogenase (G6PD) in the thrombocytes of children with ictero-hemoglobinuric favism].
    Tangheroni W, Falorni A, Cao A, Vespa M.
    Pediatria (Napoli); 1967 Feb 28; 75(1):36-47. PubMed ID: 5628738
    [No Abstract] [Full Text] [Related]

  • 20. Erythrocyte acetylcholinesterase deficiency in paroxysmal nocturnal hemoglobinuria (PNH). A comparison of the complement-sensitive and insensitive populations.
    Kunstling TR, Rosse WF.
    Blood; 1969 Apr 28; 33(4):607-16. PubMed ID: 5776206
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.