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Journal Abstract Search

114 related items for PubMed ID: 20598923

  • 21. Pain in sickle cell disease. Rates and risk factors.
    Platt OS, Thorington BD, Brambilla DJ, Milner PF, Rosse WF, Vichinsky E, Kinney TR.
    N Engl J Med; 1991 Jul 04; 325(1):11-6. PubMed ID: 1710777
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  • 22. Genetic Blood Disorders Survey in the Sultanate of Oman.
    Al-Riyami A, Ebrahim GJ.
    J Trop Pediatr; 2003 Jul 04; 49 Suppl 1():i1-20. PubMed ID: 12934793
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  • 23. Beta-S gene cluster haplotypes modulate hematologic and hemorheologic expression in sickle cell anemia. Use in predicting clinical severity.
    Powars DR, Meiselman HJ, Fisher TC, Hiti A, Johnson C.
    Am J Pediatr Hematol Oncol; 1994 Feb 04; 16(1):55-61. PubMed ID: 7508688
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  • 24. Alpha thalassemia, but not βS-globin haplotypes, influence sickle cell anemia clinical outcome in a large, single-center Brazilian cohort.
    Hatzlhofer BLD, Pereira-Martins DA, de Farias Domingos I, Arcanjo GDS, Weinhäuser I, Falcão DA, Farias ICC, de Freitas Batista JVG, Prado LPL, Oliveira JMF, Batista THC, Sobreira MJVC, de Santana RM, Araújo ABS, de Melo MA, de Ancântara BV, Coelho-Silva JL, de Moura Rafael ABL, de Lima Silva DM, Albuquerque FP, Santos MNN, Dos Anjos AC, Costa FF, da Silva Araújo A, Lucena-Araújo AR, Bezerra MAC.
    Ann Hematol; 2021 Apr 04; 100(4):921-931. PubMed ID: 33586016
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  • 25. Effect of alpha-globin genotype on the pathophysiology of sickle cell disease.
    Ballas SK.
    Pediatr Pathol Mol Med; 2001 Apr 04; 20(2):107-21. PubMed ID: 12673836
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  • 26. Appraisal of sickle-cell and thalassaemia genes in Saudi Arabia.
    el-Hazmi MA, Warsy AS.
    East Mediterr Health J; 1999 Nov 04; 5(6):1147-53. PubMed ID: 11924103
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  • 27. Early blood transfusions protect against microalbuminuria in children with sickle cell disease.
    Alvarez O, Montane B, Lopez G, Wilkinson J, Miller T.
    Pediatr Blood Cancer; 2006 Jul 04; 47(1):71-6. PubMed ID: 16261557
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  • 28. Prevalence, prevention, and treatment of microalbuminuria and proteinuria in children with sickle cell disease.
    McKie KT, Hanevold CD, Hernandez C, Waller JL, Ortiz L, McKie KM.
    J Pediatr Hematol Oncol; 2007 Mar 04; 29(3):140-4. PubMed ID: 17356390
    [Abstract] [Full Text] [Related]

  • 29. Hydroxyurea in sickle cell disease--a study of clinico-pharmacological efficacy in the Indian haplotype.
    Italia K, Jain D, Gattani S, Jijina F, Nadkarni A, Sawant P, Nair S, Mohanty D, Ghosh K, Colah R.
    Blood Cells Mol Dis; 2009 Mar 04; 42(1):25-31. PubMed ID: 18954999
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  • 30. Risk factors for conjunctival and retinal vessel alterations in sickle cell disease.
    Lima CS, Rocha EM, Silva NM, Sonatti MF, Costa FF, Saad ST.
    Acta Ophthalmol Scand; 2006 Apr 04; 84(2):234-41. PubMed ID: 16637843
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  • 34. Beta-globin gene cluster haplotypes in sickle cell patients from southwest Iran.
    Rahimi Z, Karimi M, Haghshenass M, Merat A.
    Am J Hematol; 2003 Nov 04; 74(3):156-60. PubMed ID: 14587041
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  • 36. Mortality in sickle cell disease. Life expectancy and risk factors for early death.
    Platt OS, Brambilla DJ, Rosse WF, Milner PF, Castro O, Steinberg MH, Klug PP.
    N Engl J Med; 1994 Jun 09; 330(23):1639-44. PubMed ID: 7993409
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  • 37. Prevalence and predictors of microalbuminuria in Jamaican children with sickle cell disease.
    King L, MooSang M, Miller M, Reid M.
    Arch Dis Child; 2011 Dec 09; 96(12):1135-9. PubMed ID: 21965808
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  • 38. Beta-thalassemia and sickle cell disease in culture of early erythroid precursors: hemoglobin synthesis and ultrastructural study.
    Beuzard Y, Tulliez M, Testa U, Vainchenker W, Dubart A, Tsapis A, Galacteros F, Breton-Gorius J, Rosa J.
    Blood Cells; 1981 Dec 09; 7(1):179-200. PubMed ID: 7187747
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  • 40. Determination of beta-globin gene cluster haplotypes and prevalence of alpha-thalassemia in sickle cell anemia patients in Venezuela.
    Arends A, Alvarez M, Velázquez D, Bravo M, Salazar R, Guevara JM, Castillo O.
    Am J Hematol; 2000 Jun 09; 64(2):87-90. PubMed ID: 10814985
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