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Journal Abstract Search

209 related items for PubMed ID: 6166735

  • 1. Prospective study of red blood cell indices, hemoglobin A2, and hemoglobin F in infants heterozygous for Beta-thalassemia.
    Galanello R, Melis MA, Ruggeri R, Cao A.
    J Pediatr; 1981 Jul; 99(1):105-8. PubMed ID: 6166735
    [No Abstract] [Full Text] [Related]

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  • 3. [Changes in hemoglobin fractions of pregnant women with heterozygous beta-thalassemia and iron deficiency anemia].
    Tikhonova LV.
    Akush Ginekol (Mosk); 1983 Dec; (12):41-3. PubMed ID: 6198936
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  • 6. Heterogeneity of beta/alpha ratio in Italian beta-thalassaemia heterozygotes.
    Sampietro M, Cappellini MD, Taddei MT, Fiorelli G.
    Haematologica; 1983 Dec; 68(6):703-11. PubMed ID: 6199264
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  • 8. beta-Thalassemia intermedia homozygous for normal hemoglobin A2 beta-thalassemia. Study in four families.
    Aksoy M, Bermek E, Almiş G, Kutlar A.
    Acta Haematol; 1982 Dec; 67(1):57-61. PubMed ID: 6174012
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  • 10. Compound heterozygosity of non-deletional hereditary persistence of fetal hemoglobin and deltabeta-thalassemia.
    Kalamaras A, Chassanidis C, Samara M, Papadakis MN, Vagena A, Aleporou-Marinou V, Patrinos GP, Kollia P.
    Am J Hematol; 2008 Sep; 83(9):760. PubMed ID: 18615450
    [No Abstract] [Full Text] [Related]

  • 11. Heterocellular hereditary persistence of fetal hemoglobin (HPFH). Molecular mechanisms of abnormal gamma-gene expression in association with beta thalassemia and linkage relationship with the beta-globin gene cluster.
    Giampaolo A, Mavilio F, Sposi NM, Carè A, Massa A, Cianetti L, Petrini M, Russo R, Cappellini MD, Marinucci M.
    Hum Genet; 1984 Sep; 66(2-3):151-6. PubMed ID: 6201431
    [Abstract] [Full Text] [Related]

  • 12. Sickle cell traits in Canada. Trimodal distribution of Hb S as a result of interaction with alpha-thalassaemia gene.
    Wong SC, Ali MA, Boyadjian SE.
    Acta Haematol; 1981 Sep; 65(3):157-63. PubMed ID: 6165216
    [Abstract] [Full Text] [Related]

  • 13. Globin chain synthesis analysis in obligate beta 0-thalassemia heterozygotes with isolated increase of hemoglobin A2 levels.
    Galanello R, Melis MA, Furbetta M, Angius A, Scalas MT, Paglietti E, Cao A.
    Nouv Rev Fr Hematol (1978); 1981 Sep; 23(4):193-5. PubMed ID: 7312613
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  • 14. Thalassemias: simple screening for hereditary anemias.
    Esposito NW.
    Nurse Pract; 1992 Feb; 17(2):50, 53-6, 61. PubMed ID: 1542463
    [Abstract] [Full Text] [Related]

  • 15. Indication of genotype of beta thalassemia based on hemoglobins A2 and F.
    Kumar R, Saraya AK, Choudhry VP.
    J Trop Pediatr; 1984 Jun; 30(3):168-71. PubMed ID: 6204062
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  • 16. Lasting Hb F reactivation and Hb A2 reduction induced by the treatment of Hodgkin's disease in a woman heterozygous for beta-thalassemia and the Swiss type of the heterocellular hereditary persistence of Hb F.
    Cech P, Testa U, Dubart A, Schneider P, Bachmann F, Guerrasio A, Beuzard Y, Schmidt PM, Clément F, Rosa J.
    Acta Haematol; 1982 Jun; 67(4):275-84. PubMed ID: 6180586
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  • 17. Erythroleukemia manifesting delta beta-thalassemia.
    Markham RE, Butler F, Goh K, Rowley PT.
    Hemoglobin; 1983 Jun; 7(1):71-8. PubMed ID: 6188718
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  • 18. Phenotypic effect of heterozygous alpha and beta 0-thalassemia interaction.
    Melis MA, Pirastu M, Galanello R, Furbetta M, Tuveri T, Cao A.
    Blood; 1983 Jul; 62(1):226-9. PubMed ID: 6305442
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  • 19. Partial mispairing and crossing-over between beta 0 and delta genes as the origin of the delta beta 0 thalassemia gene. A single mutational event hypothesis.
    Cantú JM, Ibarra B, Vaca G, Ramirez ML, Sánchez-Corona J.
    Hum Genet; 1979 Jun 19; 49(2):191-8. PubMed ID: 468250
    [No Abstract] [Full Text] [Related]

  • 20. Hematological and hemoglobin synthesis studies in a family with deltabeta-thalassemia trait.
    Pagnier J, Amegnizin KP, Labie D, Hayat M.
    Acta Haematol; 1979 Jun 19; 61(1):27-32. PubMed ID: 105537
    [Abstract] [Full Text] [Related]

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