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Journal Abstract Search

154 related items for PubMed ID: 14886398

  • 1. A new inherited abnormality of hemoglobin and its interaction with sickle cell hemoglobin.
    KAPLAN E, ZUELZER WW, NEEL JV.
    Blood; 1951 Dec; 6(12):1240-9. PubMed ID: 14886398
    [No Abstract] [Full Text] [Related]

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  • 5. Hemoglobin Zurich. I. A new hemoglobin anomaly associated with acute hemolytic episodes with inclusion bodies after sulfonamide therapy.
    FRICK PG, HITZIG WH, BETKE K.
    Blood; 1962 Sep; 20():261-71. PubMed ID: 13895148
    [No Abstract] [Full Text] [Related]

  • 6. Clinical manifestations of inherited abnormal hemoglobins. I. The interaction of hemoglobin-S with hemoglobin-D.
    STURGEON P, ITANO HA, BERGREN WR.
    Blood; 1955 May; 10(5):389-404. PubMed ID: 14363320
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  • 7. 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]

  • 8. Sickle-cell hemoglobin/hemoglobin-C disease. A report of three cases.
    CHESKIN LJ, SINGER M, COHEN FB.
    J Newark Beth Isr Hosp; 1962 Jul; 13():208-25. PubMed ID: 13878797
    [No Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. [Etiology of hemolytic anemia].
    Schmidt PM.
    Schweiz Med Wochenschr; 1981 Aug 15; 111(33):1201-7. PubMed ID: 7280629
    [Abstract] [Full Text] [Related]

  • 11. [Alkaline-resistant hemoglobin in constitutional hemolytic anemia].
    GOUTTAS A, TSEVRENIS H, POUNGOURAS P.
    Sang; 1953 Aug 15; 24(3):290-4. PubMed ID: 13089479
    [No Abstract] [Full Text] [Related]

  • 12. 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 15; 8(8):724-34. PubMed ID: 13066514
    [No Abstract] [Full Text] [Related]

  • 13. 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 15; 8(8):735-46. PubMed ID: 13066515
    [No Abstract] [Full Text] [Related]

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  • 15. 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 15; 75(1):197-201. PubMed ID: 14797780
    [No Abstract] [Full Text] [Related]

  • 16. [Physiological and pathological features of the red blood cells and the hemoglobin as a principle for disease manifestations].
    BETKE K.
    Dtsch Med Wochenschr; 1962 May 04; 87():909-14. PubMed ID: 13868622
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  • 17. [Associated dyshemoglobinosis S and C and recurrent pneumopathies].
    GIRAUD P, BERNARD R, ORSINI A, PINSARD N.
    Mars Med; 1962 May 04; 99():551-6. PubMed ID: 13898891
    [No Abstract] [Full Text] [Related]

  • 18. The role of surgery in sickle cell disease.
    Flye MW, Silver D.
    Surg Gynecol Obstet; 1973 Jul 04; 137(1):115-26. PubMed ID: 4576837
    [No Abstract] [Full Text] [Related]

  • 19. Hemoglobin S-C disease.
    BECKER JA.
    Am J Roentgenol Radium Ther Nucl Med; 1962 Sep 04; 88():503-11. PubMed ID: 13866343
    [No Abstract] [Full Text] [Related]

  • 20. 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 04; 22():757-69. PubMed ID: 14084634
    [No Abstract] [Full Text] [Related]

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