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Journal Abstract Search

185 related items for PubMed ID: 13041746

  • 1. Two cases of sickle cell disease presumably due to the combination of the genes for thalassemia and sickle cell hemoglobin.
    NEEL JV, ITANO HA, LAWRENCE JS.
    Blood; 1953 May; 8(5):434-43. PubMed ID: 13041746
    [No Abstract] [Full Text] [Related]

  • 2. Studies on abnormal hemoglobins. XIII. Hemoglobin S-thalassemia disease and hemoglobin C-thalassemia disease in siblings.
    SINGER K, JOSEPHSON AM, SINGER L, HELLER P, ZIMMERMAN HJ.
    Blood; 1957 Jul; 12(7):593-602. PubMed ID: 13436515
    [No Abstract] [Full Text] [Related]

  • 3. Abnormal hemoglobins; clinical disorders resulting from various combinations.
    LAWRENCE JS, VALENTINE WN.
    Calif Med; 1955 Jan; 82(1):1-5. PubMed ID: 13230906
    [Abstract] [Full Text] [Related]

  • 4. Observations on the inheritance of sickle-cell hemoglobin and hemoglobin C.
    RANNEY HM.
    J Clin Invest; 1954 Dec; 33(12):1634-41. PubMed ID: 13211820
    [No Abstract] [Full Text] [Related]

  • 5. [Some hereditary blood disorders].
    TETRY A.
    Biol Med (Paris); 1953 Jul; 42(4):317-27. PubMed ID: 13081682
    [No Abstract] [Full Text] [Related]

  • 6. THE FIRST OBSERVATION OF HOMOZYGOUS HEMOGLOBIN S-ALPHA THALASSEMIA DISEASE AND TWO TYPES OF SICKLE CELL THALASSEMIA DISEASE: (A) SICKLE CELL-ALPHA THALASSEMIA DISEASE, (B) SICKLE CELL-BETA THALASSEMIA DISEASE.
    AKSOY M.
    Blood; 1963 Dec; 22():757-69. PubMed ID: 14084634
    [No Abstract] [Full Text] [Related]

  • 7. Studies in sickle cell anemia; inheritance factor, including effect of interaction of genes for sicklemia and thalassemia.
    BANKS LO, SCOTT RB, SIMMONS J.
    AMA Am J Dis Child; 1952 Nov; 84(5):601-8. PubMed ID: 12984823
    [No Abstract] [Full Text] [Related]

  • 8. The genetics of human haemoglobin differences: problems and perspectives.
    NEEL JV.
    Ann Hum Genet; 1956 Jul; 21(1):1-30. PubMed ID: 13340556
    [No Abstract] [Full Text] [Related]

  • 9. Molecular biology of hemoglobin: its application to sickle cell anemia and thalassemia.
    Kan YW.
    Schweiz Med Wochenschr Suppl; 1991 Jul; 43():51-4. PubMed ID: 1726857
    [Abstract] [Full Text] [Related]

  • 10. Familial differences in the proportion of abnormal hemoglobin present in the sickle cell trait.
    NEEL JV, WELLS IC, ITANO HA.
    J Clin Invest; 1951 Oct; 30(10):1120-4. PubMed ID: 14888690
    [No Abstract] [Full Text] [Related]

  • 11. The human hemoglobins in health and disease.
    CHERNOFF AI.
    N Engl J Med; 1955 Sep 08; 253(10):416-23; concl. PubMed ID: 13253850
    [No Abstract] [Full Text] [Related]

  • 12. Genetic aspects of sickle cell anemia and microdrepanocytic disease.
    SILVESTRONI E, BIANCO I.
    Blood; 1952 Apr 08; 7(4):429-35. PubMed ID: 14915987
    [No Abstract] [Full Text] [Related]

  • 13. Association between sickle cell and β-thalassemia genes and hemoglobin concentration and anemia in children and non-pregnant women in Sierra Leone: ancillary analysis of data from Sierra Leone's 2013 National Micronutrient Survey.
    Wirth JP, Ansumana R, Woodruff BA, Koroma AS, Hodges MH.
    BMC Res Notes; 2018 Jan 17; 11(1):43. PubMed ID: 29343300
    [Abstract] [Full Text] [Related]

  • 14. Sickle cell haemoglobin and two types of thalassaemia in the same family.
    RUSSO G, MOLLICA F.
    Acta Haematol; 1962 Jan 17; 28():329-40. PubMed ID: 13975667
    [No Abstract] [Full Text] [Related]

  • 15. Clinical manifestations of inherited abnormal hemoglobins. I. The interaction of hemoglobin-S with hemoglobin-D.
    STURGEON P, ITANO HA, BERGREN WR.
    Blood; 1955 May 17; 10(5):389-404. PubMed ID: 14363320
    [No Abstract] [Full Text] [Related]

  • 16. Abnormal forms of hemoglobin from a genetic point of view.
    NEEL JV.
    AMA Arch Intern Med; 1956 Nov 17; 98(5):555-8. PubMed ID: 13361589
    [No Abstract] [Full Text] [Related]

  • 17. [A CASE OF MICRODREPANOCYTIC DISEASE DUE TO S HEMOGLOBIN AND A VARIETY OF MICROCYTHEMIA WITH NORMAL QUOTA OF A2 HEMOGLOBIN AND ELEVATED QUOTA OF F HEMOGLOBIN (THIRD VARIETY OF MICRODREPANOCYTIC DISEASE)].
    SILVESTRONI E, BIANCO I.
    Prog Med (Napoli); 1964 Aug 15; 20():509-13. PubMed ID: 14235120
    [No Abstract] [Full Text] [Related]

  • 18. [HOMOZYGOUS HEMOGLOBIN S AND ALPHA THALASSEMIC DISEASE].
    AKSOY M.
    Turk Tip Cemiy Mecm; 1963 Jun 15; 29():299-305. PubMed ID: 14047036
    [No Abstract] [Full Text] [Related]

  • 19. A family with S and C hemoglobins and the hereditary persistence of F hemoglobin. A comparison of C thalassemia disease with the CF syndrome.
    SCHNEIDER RG, LEVIN WC, EVERETT C.
    N Engl J Med; 1961 Dec 28; 265():1278-83. PubMed ID: 13908956
    [No Abstract] [Full Text] [Related]

  • 20. [Differential diagnostic criteria in hemoglobinosis S/beta-thalassemia].
    Kolodeĭ SV.
    Probl Gematol Pereliv Krovi; 1979 Nov 28; 24(11):11-5. PubMed ID: 504091
    [No Abstract] [Full Text] [Related]

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