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PUBMED FOR HANDHELDS

Journal Abstract Search


123 related items for PubMed ID: 8813088

  • 21.
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  • 22. Effect of alpha-globin genotype on the pathophysiology of sickle cell disease.
    Ballas SK.
    Pediatr Pathol Mol Med; 2001; 20(2):107-21. PubMed ID: 12673836
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  • 25. The interaction of alpha-thalassemia and homozygous sickle-cell disease.
    Higgs DR, Aldridge BE, Lamb J, Clegg JB, Weatherall DJ, Hayes RJ, Grandison Y, Lowrie Y, Mason KP, Serjeant BE, Serjeant GR.
    N Engl J Med; 1982 Jun 17; 306(24):1441-6. PubMed ID: 6176865
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  • 26. Avascular necrosis of the hip in children with sickle cell disease and high Hb F: magnetic resonance imaging findings and influence of alpha-thalassemia trait.
    Adekile AD, Gupta R, Yacoub F, Sinan T, Al-Bloushi M, Haider MZ.
    Acta Haematol; 2001 Jun 17; 105(1):27-31. PubMed ID: 11340250
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  • 29. A mismatched-primer polymerase chain reaction-restriction fragment length polymorphism strategy for rapid screening of the polyadenylation signal mutation alpha(T-Saudi) (AATAAA-->AATAAG) in the alpha2-globin gene.
    Jassim N, Al-Arrayed S, Gerard N, Al-Mukharraq H, Al-Ajami A, Ramasawmy R, Krishnamoorthy R.
    Hemoglobin; 1999 Aug 17; 23(3):213-20. PubMed ID: 10490133
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  • 30. Hydroxyurea alters hematological, biochemical and inflammatory biomarkers in Brazilian children with SCA: Investigating associations with βS haplotype and α-thalassemia.
    Yahouédéhou SCMA, da Guarda CC, Figueiredo CVB, Santiago RP, Carvalho SP, Fiuza LM, Ndidi US, Oliveira RM, Carvalho MOS, Nascimento VML, Rocha LC, Lyra IM, Adorno EV, Goncalves MS.
    PLoS One; 2019 Aug 17; 14(7):e0218040. PubMed ID: 31306416
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  • 31. Splenic uptake of both technetium-99m diphosphonate and technetium-99m sulfur colloid in sickle cell beta (0) thalassemia.
    Heck LL, Brittin GM.
    Clin Nucl Med; 1989 Aug 17; 14(8):557-63. PubMed ID: 2805534
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  • 32. The alpha-globin genotype does not influence sickle cell disease severity in a retrospective cross-validation study of the pediatric severity score.
    Joly P, Pondarré C, Bardel C, Francina A, Martin C.
    Eur J Haematol; 2012 Jan 17; 88(1):61-7. PubMed ID: 21910753
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  • 36. Tc-99m diphosphonate and sulfur colloid uptake by the spleen in sickle disease: interrelationship and clinical correlates: concise communication.
    Silberstein EB, DeLong S, Cline J.
    J Nucl Med; 1984 Dec 17; 25(12):1300-3. PubMed ID: 6502253
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  • 37. Characterization of nondeletion alpha-thalassemia mutations in the Greek population.
    Traeger-Synodinos J, Kanavakis E, Tzetis M, Kattamis A, Kattamis C.
    Am J Hematol; 1993 Nov 17; 44(3):162-7. PubMed ID: 8213764
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  • 38. β-globin gene cluster haplotypes in sickle cell patients from Panamá.
    Rusanova I, Cossio G, Moreno B, Javier Perea F, De Borace RG, Perea M, Escames G, Acuña-Castroviejo D.
    Am J Hum Biol; 2011 Nov 17; 23(3):377-80. PubMed ID: 21387457
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  • 39. Mutations associated with beta-thalassemia intermedia in Kuwait.
    Adekile A, Haider M, Kutlar F.
    Med Princ Pract; 2005 Nov 17; 14 Suppl 1():69-72. PubMed ID: 16103715
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  • 40. The presence of alpha-thalassaemia trait blunts the response to hydroxycarbamide in patients with sickle cell disease.
    Vasavda N, Badiger S, Rees D, Height S, Howard J, Thein SL.
    Br J Haematol; 2008 Nov 17; 143(4):589-92. PubMed ID: 18764867
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