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PUBMED FOR HANDHELDS

Journal Abstract Search


126 related items for PubMed ID: 13436509

  • 1. Studies on hemoglobin E. III. Homozygous hemoglobin E and variants of thalassemia and hemoglobin E; a family study.
    NA-NAKORN S, MINNICH V.
    Blood; 1957 Jun; 12(6):529-38. PubMed ID: 13436509
    [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. [Thalassemia-hemoglobin E disease and hypersplenism].
    AKSOY M, CETINGIL AI, KOCABALKAN N, SESTAKOF D, ALADAG T, SECER F, BOSTANCI N.
    Turk Tip Cemiy Mecm; 1962 Apr; 28():193-200. PubMed ID: 13859974
    [No Abstract] [Full Text] [Related]

  • 4. Haemoglobin E, thalassaemia, and their combination in a Muslim family of East Pakistan.
    KHALEQUE KA.
    J Trop Med Hyg; 1961 Jul; 64():171-4. PubMed ID: 13755592
    [No Abstract] [Full Text] [Related]

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

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

  • 7. Thalassaemia-haemoglobin E disease.
    SARKAR US, GHOSAL SP, CHAUDHURI JN.
    Indian J Pediatr; 1959 Oct; 26():361-70. PubMed ID: 14441753
    [No Abstract] [Full Text] [Related]

  • 8. [Microcytosis and hemoglobin a.r. in the genetics of thalassemia].
    ROMEO G.
    Boll Soc Ital Biol Sper; 1960 Mar 15; 36():219-21. PubMed ID: 14438611
    [No Abstract] [Full Text] [Related]

  • 9. [Normal slow hemoglobin A2; its relation with a new slow hemoglobin B2 fraction and its importance for the recognition of thalassemic variants which occur in families with thalassemia media and hemoglobinopathy H].
    CEPPELLINI R.
    Acta Genet Med Gemellol (Roma); 1959 Mar 15; 8():47-68. PubMed ID: 13808811
    [No Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. The demonstration of a haemoglobin E-like compound in some cases of thalassaemia.
    CROWLEY MF, MCSORLEY JG, AKSOY M, LEHMANN H.
    Vox Sang; 1957 Jan 28; 2(1):53-9. PubMed ID: 13423214
    [No Abstract] [Full Text] [Related]

  • 12. Glutathione stability test in haemoglobin E-thalassaemia disease.
    SWARUP S, GHOSH SK, CHATTERJEA JB.
    Nature; 1960 Oct 08; 188():153. PubMed ID: 13774244
    [No Abstract] [Full Text] [Related]

  • 13. The genetics of human haemoglobin differences: problems and perspectives.
    NEEL JV.
    Ann Hum Genet; 1956 Jul 08; 21(1):1-30. PubMed ID: 13340556
    [No Abstract] [Full Text] [Related]

  • 14. [Thalassemia, hemoglobin H disease and persistent Bart's hemoglobin in a Jewish family from Iraq].
    RAMOTH B, SHEBA C, FISHER S.
    Harefuah; 1960 Jan 01; 58():1-3. PubMed ID: 14436103
    [No Abstract] [Full Text] [Related]

  • 15. [Thalassemia and abnormal hemoglobins in the Aegean region of Anatolia].
    GOKSEL V, TARTAROGLU N.
    Rev Med Moyen Orient; 1962 Jan 01; 19():58-64. PubMed ID: 13899597
    [No Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. [Electrophoretic research on hemoglobin in a family with hereditary leptocytosis].
    SOKMEN C.
    Minerva Med; 1956 Jul 04; 47(53):6-7. PubMed ID: 13348357
    [No Abstract] [Full Text] [Related]

  • 18. Interactions of unstable hemoglobin Rush with thalassemia and hemoglobin E result in thalassemia intermedia.
    Huang K, Ge S, Yi W, Bi H, Lin K, Sun H, Huang X, Chu J, Ma S, Yang Z.
    Hematology; 2019 Dec 04; 24(1):459-466. PubMed ID: 31124399
    [Abstract] [Full Text] [Related]

  • 19. Thalassaemia in a Scottish family.
    ISRAELS LG, SUDERMAN HJ, HOOGSTRATEN J.
    Lancet; 1955 Dec 24; 269(6904):1318-20. PubMed ID: 13272382
    [No Abstract] [Full Text] [Related]

  • 20. Thalassemia in Jews from Kurdistan.
    MATOTH Y, SHAMIR Z, FREUNDLICH E.
    Blood; 1955 Feb 24; 10(2):176-89. PubMed ID: 13230170
    [No Abstract] [Full Text] [Related]


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