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Journal Abstract Search

195 related items for PubMed ID: 13929130

  • 1. Study of a family possessing hemoglobin C, classical thalassemia and the abnormal minor hemoglobin component A2.
    LEE RC, HUISMAN TH.
    Am J Hum Genet; 1963 Mar; 15(1):69-73. PubMed ID: 13929130
    [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. Studies on abnormal hemoglobins. X. A new syndrome: hemoglobin C-thalassemia disease.
    SINGER K, KRAUS AP, SINGER L, RUBINSTEIN HM, GOLDBERG SR.
    Blood; 1954 Nov; 9(11):1032-46. PubMed ID: 13208755
    [No Abstract] [Full Text] [Related]

  • 4. [On the behavior of different types of hemoglobin (Hb A, A2, F, S and "Bart's") in thalassemia, drepanocytosis and microdrepanocythemia].
    VENTRUTO V, DE ROSA L, CIMINO R, QUATTRIN N.
    Schweiz Med Wochenschr; 1962 Oct 20; 92():1322-4. PubMed ID: 13996677
    [No Abstract] [Full Text] [Related]

  • 5. [First case of hemoglobin C-thalassemia in Italy].
    PEROSA L, MANGANELLI G, DALFINO G.
    Boll Soc Ital Biol Sper; 1960 Feb 15; 36():93-6. PubMed ID: 14431935
    [No Abstract] [Full Text] [Related]

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

  • 7. [THE BEHAVIOR OF THE HEMOGLOBIN A2 FRACTION DURING ALPHA AND BETA THALASSEMIA AND IN SOME OTHER NON-THALASSEMIC BLOOD DISEASES].
    SOFFRITTI E, MALAGUTI R.
    Arcisp S Anna Ferrara; 1964 Feb 15; 17():373-83. PubMed ID: 14170667
    [No Abstract] [Full Text] [Related]

  • 8. 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 15; 12(3):238-50. PubMed ID: 13403987
    [No Abstract] [Full Text] [Related]

  • 9. Thalassemia-hemoglobin C disease; a new syndrome presumably due to the combination of the genes for thalassemia and hemoglobin C.
    ZUELZER WW, KAPLAN E.
    Blood; 1954 Nov 15; 9(11):1047-54. PubMed ID: 13208756
    [No Abstract] [Full Text] [Related]

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

  • 11. Studies on abnormal hemoglobins. XI. Sickle cell-thalassemia disease in the Negro; the significance of the S+A+F and S+A patterns obtained by hemoglobin analysis.
    SINGER K, SINGER L, GOLDBERG SR.
    Blood; 1955 May 15; 10(5):405-15. PubMed ID: 14363321
    [No Abstract] [Full Text] [Related]

  • 12. [RELATIONS BETWEEN HEMOGLOBIN A2 AND HEMOGLOBIN F IN PATIENTS WITH THALASSEMIA].
    SCHETTINI F, MELONI T.
    Haematologica; 1964 May 15; 49():471-87. PubMed ID: 14213263
    [No Abstract] [Full Text] [Related]

  • 13. [Hemoglobin F and hemoglobin A2 increase in the Swiss population].
    MARTI HR, BUETLER R.
    Acta Haematol; 1961 May 15; 26():65-74. PubMed ID: 14470305
    [No Abstract] [Full Text] [Related]

  • 14. 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 15; 17():393-408. PubMed ID: 13788925
    [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 15; 10(5):389-404. PubMed ID: 14363320
    [No Abstract] [Full Text] [Related]

  • 16. [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]

  • 17. Inclusions of hemoglobin erythroblasts and erythrocytes of thalassemia.
    FESSAS P.
    Blood; 1963 Jan 01; 21():21-32. PubMed ID: 13944958
    [No Abstract] [Full Text] [Related]

  • 18. Abnormal hemoglobins; clinical disorders resulting from various combinations.
    LAWRENCE JS, VALENTINE WN.
    Calif Med; 1955 Jan 01; 82(1):1-5. PubMed ID: 13230906
    [Abstract] [Full Text] [Related]

  • 19. [High hemoglobin A-2 disease and microcythemia].
    LUCCI R, SOFFRITTI E, BORGATTI L, CABASSA N.
    Acta Genet Med Gemellol (Roma); 1962 Jan 01; 11():71-88. PubMed ID: 14467126
    [No Abstract] [Full Text] [Related]

  • 20. [HEMOGLOBIN A2. IMPORTANCE OF ITS RESEARCH IN MINIMAL THALASSEMIA].
    GIRAUD P, ORSINI A, RAYBAUD C.
    Pediatrie; 1964 Jan 01; 19():835-9. PubMed ID: 14231366
    [No Abstract] [Full Text] [Related]

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