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Journal Abstract Search

818 related items for PubMed ID: 14084634

  • 1. 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; 22():757-69. PubMed ID: 14084634
    [No Abstract] [Full Text] [Related]

  • 2. 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
    [No Abstract] [Full Text] [Related]

  • 3. [TYPES OF SICKLE CELL- THALASSEMIC DISEASES. A. SICKLE CELL-BETA THALASSEMIA. B. SICKLE CELL-ALPHA THALASSEMIA. STUDY OF 6 CASES IN 5 FAMILIES].
    AKSOY M.
    Turk Tip Cemiy Mecm; 1963 Jun; 29():313-20. PubMed ID: 14047038
    [No Abstract] [Full Text] [Related]

  • 4. 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; 10(5):405-15. PubMed ID: 14363321
    [No Abstract] [Full Text] [Related]

  • 5. Sickle cell haemoglobin and two types of thalassaemia in the same family.
    RUSSO G, MOLLICA F.
    Acta Haematol; 1962 May; 28():329-40. PubMed ID: 13975667
    [No Abstract] [Full Text] [Related]

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

  • 7. [HOMOZYGOUS HEMOGLOBIN S AND ALPHA THALASSEMIC DISEASE].
    AKSOY M.
    Turk Tip Cemiy Mecm; 1963 Jun; 29():299-305. PubMed ID: 14047036
    [No Abstract] [Full Text] [Related]

  • 8. [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]

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  • 11. OCCURRENCE OF HAEMOGLOBIN H AND HAEMOGLOBIN BART'S IN ALPHA-THALASSEMIA: A FAMILY WITH 2 POSSIBLE HOMOZYGOUS CASES WITH G-6-PD-DEFICIENCY.
    HELLEMAN PW, PUNT K, VERLOOP MC.
    Nature; 1964 Mar 07; 201():1039-40. PubMed ID: 14191584
    [No Abstract] [Full Text] [Related]

  • 12. Sickle cell syndromes. II. The sickle cell anemia-alpha-thalassemia syndrome.
    Honig GR, Koshy M, Mason RG, Vida LN.
    J Pediatr; 1978 Apr 07; 92(4):556-61. PubMed ID: 633012
    [Abstract] [Full Text] [Related]

  • 13. Genetic Background of the Sickle Cell Disease Pediatric Population of Dakar, Senegal, and Characterization of a Novel Frameshift β-Thalassemia Mutation [HBB: c.265_266del; p.Leu89Glufs*2].
    Gueye Tall F, Martin C, Malick Ndour EH, Déme Ly I, Renoux C, Chillotti L, Veyrenche N, Connes P, Madieye Gueye P, Ndiaye Diallo R, Lacan P, Diagne I, Amadou Diop P, Cissé A, Lopez Sall P, Joly P.
    Hemoglobin; 2017 Mar 07; 41(2):89-95. PubMed ID: 28670947
    [Abstract] [Full Text] [Related]

  • 14. Sickle cell anemia and α-thalassemia: a modulating factor in homozygous HbS/S patients in Oman.
    Hassan SM, Al Muslahi M, Al Riyami M, Bakker E, Harteveld CL, Giordano PC.
    Eur J Med Genet; 2014 Mar 07; 57(11-12):603-6. PubMed ID: 25266642
    [Abstract] [Full Text] [Related]

  • 15. Studies on abnormal hemoglobins. III. The interrelationship of type S (sickle cell) hemoglobin and type F (alkali resistant) hemoglobin in sickle cell anemia.
    SINGER K, CHERNOFF AI.
    Blood; 1952 Jan 07; 7(1):47-52. PubMed ID: 14886409
    [No Abstract] [Full Text] [Related]

  • 16. Analysis of mRNA from red cells of patients with thalassemia and hemoglobin variants.
    Smetanina NS, Molchanova TP, Huisman TH.
    Hemoglobin; 1997 Sep 07; 21(5):437-67. PubMed ID: 9322078
    [Abstract] [Full Text] [Related]

  • 17. [A CASE OF MICRODREPANOCYTIC DISEASE DUE TO S HEMOGLOBIN AND A VARIETY OF MICROCYTHEMIA WITH NORMAL QUOTA OF A2 HEMOGLOBIN AND ELEVATED QUOTA OF F HEMOGLOBIN (THIRD VARIETY OF MICRODREPANOCYTIC DISEASE)].
    SILVESTRONI E, BIANCO I.
    Prog Med (Napoli); 1964 Aug 15; 20():509-13. PubMed ID: 14235120
    [No Abstract] [Full Text] [Related]

  • 18. [Serological research on the antigen power of some types of normal and pathological human hemoglobin. I. Hemoglobin of Cooley's anemia and of sickle cell anemia].
    VECCHIO F, BARBAGALLO E.
    Pediatria (Napoli); 1950 Aug 15; 58(7-8):481-97. PubMed ID: 14797314
    [No Abstract] [Full Text] [Related]

  • 19. [THALASSEMIA MINOR HB-S. BASED ON CASES IN ONE FAMILY].
    OBRADOV S, MUSAFIJA A, DUGUMOVIC Z.
    Med Arh; 1964 Aug 15; 18():47-56. PubMed ID: 14311906
    [No Abstract] [Full Text] [Related]

  • 20. Modification of hemoglobin H disease by sickle trait.
    Matthay KK, Mentzer WC, Dozy AM, Kan YW, Bainton DF.
    J Clin Invest; 1979 Oct 15; 64(4):1024-32. PubMed ID: 479366
    [Abstract] [Full Text] [Related]

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