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Journal Abstract Search

311 related items for PubMed ID: 13032196

  • 1. Studies on abnormal hemoglobins. VI. Electrophoretic demonstration of type S (sickle cell) hemoglobin in erythrocytes incapable of showing the sickle cell phenomenon.
    SINGER K, FISHER B.
    Blood; 1953 Mar; 8(3):270-5. PubMed ID: 13032196
    [No Abstract] [Full Text] [Related]

  • 2. Singer K, Fisher B. Studies on abnormal hemoglobins, VI: electrophoretic demonstration of type S (sickle cell) hemoglobin in erythrocytes incapable of showing the sickle cell phenomenon. Blood. 1953;8(3):270-275.
    Blood; 2016 Feb 18; 127(7):791. PubMed ID: 26893392
    [No Abstract] [Full Text] [Related]

  • 3. Studies on abnormal hemoglobins. III. The interrelationship of type S (sickle cell) hemoglobin and type F (alkali resistant) hemoglobin in sickle cell anemia.
    SINGER K, CHERNOFF AI.
    Blood; 1952 Jan 18; 7(1):47-52. PubMed ID: 14886409
    [No Abstract] [Full Text] [Related]

  • 4. Studies on abnormal hemoglobins. V. The distribution of type S, sickle cell, hemoglobin and type F, alkali resistant, hemoglobin within the red cell population in sickle cell anemia.
    SINGER K, FISHER B.
    Blood; 1952 Dec 18; 7(12):1216-26. PubMed ID: 12997538
    [No Abstract] [Full Text] [Related]

  • 5. Clinical manifestations of inherited abnormal hemoglobins. I. The interaction of hemoglobin-S with hemoglobin-D.
    STURGEON P, ITANO HA, BERGREN WR.
    Blood; 1955 May 18; 10(5):389-404. PubMed ID: 14363320
    [No Abstract] [Full Text] [Related]

  • 6. Further studies on hemoglobin C. I. A description of three additional families segregating for hemoglobin C and sickle cell hemoglobin.
    NEEL JV, KAPLAN E, ZUELZER WW.
    Blood; 1953 Aug 18; 8(8):724-34. PubMed ID: 13066514
    [No Abstract] [Full Text] [Related]

  • 7. Further studies on hemoglobin C. II. The hematologic effects of hemoglobin C alone and in combination with sickle cell hemoglobin.
    KAPLAN E, ZUELZER WW, NEEL JV.
    Blood; 1953 Aug 18; 8(8):735-46. PubMed ID: 13066515
    [No Abstract] [Full Text] [Related]

  • 8. Deoxyhemoglobin S: solubility vs. erythrocyte sickling.
    Vedvick TS, Koenig HM, Itano HA.
    Clin Biochem; 1975 Aug 18; 8(4):288-90. PubMed ID: 1157297
    [No Abstract] [Full Text] [Related]

  • 9. Studies on the destruction of red blood cells. VIII. Molecular orientation in sickle cell hemoglobin solutions.
    HARRIS JW.
    Proc Soc Exp Biol Med; 1950 Oct 18; 75(1):197-201. PubMed ID: 14797780
    [No Abstract] [Full Text] [Related]

  • 10. Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation.
    SINGER K, CHERNOFF AI, SINGER L.
    Blood; 1951 May 18; 6(5):413-28. PubMed ID: 14830637
    [No Abstract] [Full Text] [Related]

  • 11. 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 18; 22():757-69. PubMed ID: 14084634
    [No Abstract] [Full Text] [Related]

  • 12. Cyanate and sickle-cell disease.
    Cerami A, Peterson CM.
    Sci Am; 1975 Apr 18; 232(4):44-50. PubMed ID: 1114310
    [No Abstract] [Full Text] [Related]

  • 13. Studies on abnormal hemoglobins. VII. The composition of the non-S hemoglobin fraction in sickle-cell anemia bloods; a comparative quantitative study by the methods of electrophoresis and alkali denaturation.
    SINGER K, FISHER B.
    J Lab Clin Med; 1953 Aug 18; 42(2):193-204. PubMed ID: 13069865
    [No Abstract] [Full Text] [Related]

  • 14. INTRAERYTHROCYTIC HEMOGLOBIN CRYSTALS IN SICKLE CELL-HEMOGLOBIN C DISEASE.
    DIGGS LW, BELL A.
    Blood; 1965 Feb 18; 25():218-23. PubMed ID: 14267697
    [No Abstract] [Full Text] [Related]

  • 15. Zone electrophoresis of abnormal hemoglobins; separation on paper of hemoglobins associated with sickle cell disease.
    BERGREN WR, STURGEON P, ITANO HA.
    Acta Haematol; 1954 Sep 18; 12(3):160-8. PubMed ID: 13196930
    [No Abstract] [Full Text] [Related]

  • 16. Altered filterability of CPD-stored sickle trait donor blood.
    Hipp MJ, Scott RB.
    Transfusion; 1974 Sep 18; 14(5):447-52. PubMed ID: 4411925
    [No Abstract] [Full Text] [Related]

  • 17. Editorial: Delay time of gelation: a possible determinant of clinical severity in sickle cell disease.
    Eaton WA, Hofrichter J, Ross PD.
    Blood; 1976 Apr 18; 47(4):621-7. PubMed ID: 1260125
    [No Abstract] [Full Text] [Related]

  • 18. Deoxyhemoglobin S polymer formation in sickle cells.
    Schechter AN, Noguchi CT, Rodgers GP.
    Blood; 1986 Dec 18; 68(6):1415-6. PubMed ID: 3779105
    [No Abstract] [Full Text] [Related]

  • 19. [The hemoglobins of sickle-cell blood].
    ROCHE J, DERRIEN Y, GALLAIS P, ROQUES M.
    C R Seances Soc Biol Fil; 1952 Jun 18; 146(11-12):889-91. PubMed ID: 12998291
    [No Abstract] [Full Text] [Related]

  • 20. RHEOLOGY OF PACKED RED BLOOD CELLS CONTAINING HEMOGLOBINS A-A, S-A, AND S-S.
    DINTENFASS L.
    J Lab Clin Med; 1964 Oct 18; 64():594-600. PubMed ID: 14233148
    [No Abstract] [Full Text] [Related]

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