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Journal Abstract Search

229 related items for PubMed ID: 1752955

  • 1. Effects of alpha-thalassemia and sickle polymerization tendency on the urine-concentrating defect of individuals with sickle cell trait.
    Gupta AK, Kirchner KA, Nicholson R, Adams JG, Schechter AN, Noguchi CT, Steinberg MH.
    J Clin Invest; 1991 Dec; 88(6):1963-8. PubMed ID: 1752955
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  • 2. Intracellular polymerization of sickle hemoglobin: disease severity and therapeutic goals.
    Noguchi CT, Rodgers GP, Schechter AN.
    Prog Clin Biol Res; 1987 Dec; 240():381-91. PubMed ID: 3615501
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  • 3. Percentage of HbS among cases of sickle-cell trait in Basra, Iraq.
    al-Shakour AA, al-Suhail AA.
    East Mediterr Health J; 2000 Dec; 6(2-3):233-7. PubMed ID: 11556007
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  • 4. Sickle cell trait revisited.
    Harkness DR.
    Am J Med; 1989 Sep; 87(3N):30N-34N. PubMed ID: 2486530
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  • 5. Haematological status of blood-donors with sickle cell trait and alpha thalassaemia in northern Nigeria.
    Niazi GA, Fleming AF.
    East Afr Med J; 1989 Dec; 66(12):824-9. PubMed ID: 2612414
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  • 6. Renal acidification in sickle-cell disease.
    Oster JR, Lespier LE, Lee SM, Pellegrini EL, Vaamonde CA.
    J Lab Clin Med; 1976 Sep; 88(3):389-401. PubMed ID: 8574
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  • 7. Studies on kidney function in subjects exposed to organic solvents. II. The effect of desmopressin in a concentration test and the effect of exposure to organic solvents on renal concentrating ability.
    Askergren A, Allgën LG, Bergström J.
    Acta Med Scand; 1981 Sep; 209(6):485-8. PubMed ID: 7257866
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  • 8. Renal response to potassium loading in sickle cell trait.
    Oster JR, Lanier DC, Vaamonde CA.
    Arch Intern Med; 1980 Apr; 140(4):534-6. PubMed ID: 7362386
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  • 9. Optimal haematocrit in subjects with normal haemoglobin genotype (HbAA), sickle cell trait (HbAS), and homozygous sickle cell disease (HbSS).
    Bowers AS, Pepple DJ, Reid HL.
    Clin Hemorheol Microcirc; 2011 Apr; 47(4):253-60. PubMed ID: 21654054
    [Abstract] [Full Text] [Related]

  • 10. Trimodal distribution of HbS levels in sickle heterozygotes--an useful predictor of the alpha-genotype for population screening.
    Mukherjee MB, Surve R, Tamankar A, Colah R, Mohanty D.
    Indian J Med Res; 1998 Dec; 108():285-90. PubMed ID: 9919012
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  • 11. Renal concentrating capacity as a marker for glomerular filtration rate.
    García Nieto VM, Yanes MI, Zamorano MM, González MJ, Aros CP, Garin EH.
    Acta Paediatr; 2008 Jan; 97(1):96-9. PubMed ID: 18076717
    [Abstract] [Full Text] [Related]

  • 12. Overview of pathophysiology and rationale for treatment of sickle cell anemia.
    Rodgers GP.
    Semin Hematol; 1997 Jul; 34(3 Suppl 3):2-7. PubMed ID: 9317195
    [Abstract] [Full Text] [Related]

  • 13. Prevalence of -alpha(3.7) and alpha alpha alpha(anti3.7) alleles in sickle cell trait and beta-thalassemia patients in Mexico.
    Nava MP, Ibarra B, Magaña MT, de la Luz Chávez M, Perea FJ.
    Blood Cells Mol Dis; 2006 Jul; 36(2):255-8. PubMed ID: 16466950
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  • 15. Overnight testing of renal concentrating capacity in children using desmopressin tablets: sensitivity, repeatability and non-inferiority versus intranasal spray.
    Asa Rembratt, Jens-Kristian Jensen, Kjell Tullus, Staffan Mårild, Renal Concentrating Capacity Test (RCCT) study group.
    Scand J Urol Nephrol; 2008 Jul; 42(3):274-7. PubMed ID: 17943639
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