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Journal Abstract Search

156 related items for PubMed ID: 14438611

  • 1. [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]

  • 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 15; 12(7):593-602. PubMed ID: 13436515
    [No Abstract] [Full Text] [Related]

  • 3. [High hemoglobin A-2 disease and microcythemia].
    LUCCI R, SOFFRITTI E, BORGATTI L, CABASSA N.
    Acta Genet Med Gemellol (Roma); 1962 Jan 15; 11():71-88. PubMed ID: 14467126
    [No Abstract] [Full Text] [Related]

  • 4. [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 Jan 15; 8():47-68. PubMed ID: 13808811
    [No Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. 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]

  • 7. [Thalassemia and abnormal hemoglobins in the Aegean region of Anatolia].
    GOKSEL V, TARTAROGLU N.
    Rev Med Moyen Orient; 1962 Dec 28; 19():58-64. PubMed ID: 13899597
    [No Abstract] [Full Text] [Related]

  • 8. [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; 28():193-200. PubMed ID: 13859974
    [No Abstract] [Full Text] [Related]

  • 9. [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]

  • 10. 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]

  • 11. The thalassaemia syndromes. I. Thalassaemia minor with large amount of fetal haemoglobin. Study of a family.
    AKSOY M, EGRIBOZLU A, ALPUSTUN H.
    Acta Haematol; 1961 Feb 01; 25():136-42. PubMed ID: 13681961
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Two families showing interaction of haemoglobin C or thalassaemia with high foetal haemoglobin in adults.
    KRAUS AP, KOCH B, BURCKETT L.
    Br Med J; 1961 May 20; 1(5237):1434-6. PubMed ID: 13754061
    [No Abstract] [Full Text] [Related]

  • 14. Haemoglobin E, thalassaemia, and their combination in a Muslim family of East Pakistan.
    KHALEQUE KA.
    J Trop Med Hyg; 1961 Jul 20; 64():171-4. PubMed ID: 13755592
    [No Abstract] [Full Text] [Related]

  • 15. Can haemoglobin A be synthesized in certain cases of thalassemia major?
    MASSIMO L.
    Panminerva Med; 1960 Dec 20; 2():602-3. PubMed ID: 13767931
    [No Abstract] [Full Text] [Related]

  • 16. 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 20; 22():757-69. PubMed ID: 14084634
    [No Abstract] [Full Text] [Related]

  • 17. Reciprocal relationship of hemoglobins A2 and F in beta chain thalassemias, a key to the genetic control of hemoglobin F.
    ZUELZER WW, ROBINSON AR, BOOKER CR.
    Blood; 1961 Apr 20; 17():393-408. PubMed ID: 13788925
    [No Abstract] [Full Text] [Related]

  • 18. Abnormal forms of hemoglobin from a genetic point of view.
    NEEL JV.
    AMA Arch Intern Med; 1956 Nov 20; 98(5):555-8. PubMed ID: 13361589
    [No Abstract] [Full Text] [Related]

  • 19. 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 20; 12(6):529-38. PubMed ID: 13436509
    [No Abstract] [Full Text] [Related]

  • 20. [Some hereditary blood disorders].
    TETRY A.
    Biol Med (Paris); 1953 Jul 20; 42(4):317-27. PubMed ID: 13081682
    [No Abstract] [Full Text] [Related]

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