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Journal Abstract Search

171 related items for PubMed ID: 13312885

  • 1. Hemoglobin-S-thalassemia disease; report of a case in a Negro child.
    SHIELDS GS, WETHERS D, GAVIS G, WATSON RJ.
    AMA J Dis Child; 1956 May; 91(5):485-9. PubMed ID: 13312885
    [No Abstract] [Full Text] [Related]

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  • 3. Hb.S-thalassaemia disease in India.
    CHATTERJEA JB, SWARUP S, GHOSH SK, RAY RN.
    J Indian Med Assoc; 1958 Jan 01; 30(1):4-8. PubMed ID: 13514085
    [No Abstract] [Full Text] [Related]

  • 4. Benign sickle cell-thalassemia disease and cryptic thalassemia in a Negro family.
    REYNOLDS WA.
    Ann Intern Med; 1962 Jul 01; 57():121-8. PubMed ID: 14491730
    [No Abstract] [Full Text] [Related]

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  • 6. 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 01; 12(7):593-602. PubMed ID: 13436515
    [No Abstract] [Full Text] [Related]

  • 7. Combinations of hemoglobin G, hemoglobin S and thalassemia occurring in one family.
    SCHWARTZ HC, SPAET TH, ZUELZER WW, NEEL JV, ROBINSON AR, KAUFMAN SF.
    Blood; 1957 Mar 01; 12(3):238-50. PubMed ID: 13403987
    [No Abstract] [Full Text] [Related]

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  • 10. 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 01; 22():757-69. PubMed ID: 14084634
    [No Abstract] [Full Text] [Related]

  • 11. [Micro cell anemia (sickle-thalassemia)].
    SCHAPOSNIK F, BOTTINO NR, PALATNIK M, PELUFFO RO, CHALAR O.
    Rev Clin Esp; 1958 Mar 15; 68(5):284-94. PubMed ID: 13555048
    [No Abstract] [Full Text] [Related]

  • 12. [On a case of association of thalassemia and "hereditary persistence of fetal hemoglobin"].
    MANGANELLI G, DALFINO G, TANNOIA N.
    Haematologica; 1962 Mar 15; 47():353-66. PubMed ID: 14469260
    [No Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. Sickle cell haemoglobin and two types of thalassaemia in the same family.
    RUSSO G, MOLLICA F.
    Acta Haematol; 1962 Dec 28; 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 28; 10(5):389-404. PubMed ID: 14363320
    [No Abstract] [Full Text] [Related]

  • 16. [A case of falciform anemia].
    MARCOS JR, TEMESIO N, RUOCCO GG.
    Arch Pediatr Urug; 1962 Jun 28; 33():371-6. PubMed ID: 13932898
    [No Abstract] [Full Text] [Related]

  • 17. Haemoglobin D in a Persian girl: presumably the first case of haemoglobin-D-thalassaemia.
    HYNES M, LEHMANN H.
    Br Med J; 1956 Oct 20; 2(4998):923-4. PubMed ID: 13364358
    [No Abstract] [Full Text] [Related]

  • 18. Hemoglobin H associated with an uncommon variant of thalassemia trait.
    DITTMAN WA, HAUT A, WINTROBE MM, CARTWRIGHT GE.
    Blood; 1960 Jul 20; 16():975-83. PubMed ID: 13816949
    [No Abstract] [Full Text] [Related]

  • 19. Sickling of erythrocytes in a patient with thalassemia-hemoglobin-I disease.
    ATWATER J, SCHWARTZ IR, ERSLEV AJ, MONTGOMERY TL, TOCANTINS LM.
    N Engl J Med; 1960 Dec 15; 263():1215-23. PubMed ID: 13685016
    [No Abstract] [Full Text] [Related]

  • 20. Hemoglobin H-thalassemia disease.
    WOLFF JA, MICHAELS RH, VON HOFF FH.
    Blood; 1958 May 15; 13(5):492-501. PubMed ID: 13535929
    [No Abstract] [Full Text] [Related]

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