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PUBMED FOR HANDHELDS

Journal Abstract Search


178 related items for PubMed ID: 4874574

  • 1. [Human genetics in hematological disorders].
    Fujiki N, Shibuya Y, Saito T, Takebayashi M, Mibayashi E.
    Saishin Igaku; 1967 Dec 10; 22(12):2676-85. PubMed ID: 4874574
    [No Abstract] [Full Text] [Related]

  • 2. Erythrocyte pyruvate kinase deficiency. A case of severe congenital hemolytic anemia.
    O'Connor TA, Monzon CM, Clark FI.
    Mo Med; 1989 Feb 10; 86(2):92-4. PubMed ID: 2761512
    [Abstract] [Full Text] [Related]

  • 3. [Hematologic enzymology].
    Löhr GW.
    Helv Med Acta; 1963 Nov 10; 30(4):428-48. PubMed ID: 5879107
    [No Abstract] [Full Text] [Related]

  • 4. Red cell enzymopathies as a model of inborn errors of metabolism.
    Miwa S, Kanno H, Hirono A, Fujii H.
    Southeast Asian J Trop Med Public Health; 1995 Nov 10; 26 Suppl 1():112-9. PubMed ID: 8629088
    [Abstract] [Full Text] [Related]

  • 5. Familial haemolytic anaemia due to pyruvate kinase deficiency.
    Staal GE, Sybesma HB, Cameron AR, Milligen-Boersma L, Moes M.
    Folia Med Neerl; 1971 Nov 10; 14(2):72-6. PubMed ID: 5559126
    [No Abstract] [Full Text] [Related]

  • 6. Enzyme assays in diseases of erythrocytes.
    Prankerd TA.
    J Clin Pathol Suppl (Assoc Clin Pathol); 1970 Nov 10; 4():71-4. PubMed ID: 4949770
    [No Abstract] [Full Text] [Related]

  • 7. Genes and geography.
    Waldenstrom JG.
    Nouv Rev Fr Hematol Blood Cells; 1977 Nov 10; 18(2):275-83. PubMed ID: 917829
    [Abstract] [Full Text] [Related]

  • 8. [A family study on pyruvate kinase deficiency anemia].
    Helbig W, Jacobasch G.
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1969 Nov 10; 91(1):65-9. PubMed ID: 4180965
    [No Abstract] [Full Text] [Related]

  • 9. [Constitutional hemolytic anemia due to pyruvate kinase deficiency. Study of 2 families].
    Bauters F, Durocher A, Caulier MT, Fournier A, Goudemand M.
    Lille Med; 1974 May 10; 19(5):578-83. PubMed ID: 4431277
    [No Abstract] [Full Text] [Related]

  • 10. Seminars in hematology.
    Valentine WN.
    Semin Hematol; 1971 Oct 10; 8(4):307-10. PubMed ID: 5127631
    [No Abstract] [Full Text] [Related]

  • 11. [Hereditary blood diseases].
    Ikkala E.
    Duodecim; 1968 Oct 10; 84(6):434-48. PubMed ID: 5671647
    [No Abstract] [Full Text] [Related]

  • 12. [Congenital non-spherocytic anemias].
    Vacca G.
    Minerva Med; 1968 Nov 03; 59(88):4727-30. PubMed ID: 5697156
    [No Abstract] [Full Text] [Related]

  • 13. Animal models of human erythrocyte metabolic abnormalities.
    Smith JE.
    Clin Haematol; 1981 Feb 03; 10(1):239-51. PubMed ID: 6111407
    [No Abstract] [Full Text] [Related]

  • 14. [Genetic injuries in 2 families with congenital methemoglobinemia caused by diaphorase I deficiency].
    Pedrinazzi RC, Della Cella G, Famularo L, Cerruti Mainardi P, Borrone C.
    Minerva Pediatr; 1969 May 05; 21(18):800-4. PubMed ID: 5404915
    [No Abstract] [Full Text] [Related]

  • 15. [Biologic study of a case of Pelger-Huet anomaly and another of Chediak-Higashi disease].
    Salazar-Mallén M, Mitrani-Levy D, Amezcua E.
    Gac Med Mex; 1969 Sep 05; 99(9):828-35. PubMed ID: 5345021
    [No Abstract] [Full Text] [Related]

  • 16. Inherited variations in leukocytes.
    Davidson WM.
    Semin Hematol; 1968 Jul 05; 5(3):255-74. PubMed ID: 4232764
    [No Abstract] [Full Text] [Related]

  • 17. Genetic factors in relation to drugs.
    Peters JH.
    Annu Rev Pharmacol; 1968 Jul 05; 8():427-52. PubMed ID: 4875398
    [No Abstract] [Full Text] [Related]

  • 18. The imitation of hereditary blood anomalies by acquired hematological disorders.
    Wechsler L.
    Isr J Med Sci; 1965 Jul 05; 1(4):783-6. PubMed ID: 5216386
    [No Abstract] [Full Text] [Related]

  • 19. [The clinical picture of erythropathies].
    Heilmeyer L.
    Folia Haematol (Frankf); 1964 Jul 05; 9(3):317-37. PubMed ID: 5888807
    [No Abstract] [Full Text] [Related]

  • 20. [Pyruvate kinase deficiciency (author's transl)].
    Miwa S.
    Rinsho Ketsueki; 1973 Dec 05; 14(0):1325-30. PubMed ID: 4807678
    [No Abstract] [Full Text] [Related]


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