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Journal Abstract Search

442 related items for PubMed ID: 2423018

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  • 3. New insights provided by a comparison of impaired deformability with erythrocyte oxidative stress for sickle cell disease.
    Barodka VM, Nagababu E, Mohanty JG, Nyhan D, Berkowitz DE, Rifkind JM, Strouse JJ.
    Blood Cells Mol Dis; 2014 Apr; 52(4):230-5. PubMed ID: 24246527
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  • 4. Influence of plasma and red cell factors on the rheologic properties of oxygenated sickle blood during clinical steady state.
    Morris CL, Gruppo RA, Shukla R, Rucknagel DL.
    J Lab Clin Med; 1991 Oct; 118(4):332-42. PubMed ID: 1940575
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  • 5. Contributions of sickle hemoglobin polymer and sickle cell membranes to impaired filterability.
    Hiruma H, Noguchi CT, Uyesaka N, Schechter AN, Rodgers GP.
    Am J Physiol; 1995 May; 268(5 Pt 2):H2003-8. PubMed ID: 7771550
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  • 6. [Biological profile of sickle cell anemia in Morocco. A propos of 85 cases].
    Omari M, Naji M, Agoumi N.
    Maghrib Tibbi; 1982 May; 4(2-3):175-82. PubMed ID: 7182694
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  • 8. Sickle cell syndromes. I. Hemoglobin SC-alpha-thalassemia.
    Honig GR, Gunay U, Mason RG, Vida LN, Ferenc C.
    Pediatr Res; 1976 Jun; 10(6):613-20. PubMed ID: 1272638
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  • 12. Alpha thalassemia changes erythrocyte heterogeneity in sickle cell disease.
    Noguchi CT, Dover GJ, Rodgers GP, Serjeant GR, Antonarakis SE, Anagnou NP, Higgs DR, Weatherall DJ, Schechter AN.
    J Clin Invest; 1985 May; 75(5):1632-7. PubMed ID: 2581999
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  • 16. The effect of abnormal hemoglobins on the membrane regulation of cell hydration.
    Clark MR, Shohet SB.
    Tex Rep Biol Med; 1985 May; 40():417-29. PubMed ID: 7034277
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  • 19. Value of screening umbilical cord blood for hemoglobinopathy.
    Lobel JS, Cameron BF, Johnson E, Smith D, Kalinyak K.
    Pediatrics; 1989 May; 83(5 Pt 2):823-6. PubMed ID: 2717309
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