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Journal Abstract Search

104 related items for PubMed ID: 7534433

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  • 23. Effects of hydroxyurea on the membrane of erythrocytes and platelets in sickle cell anemia.
    Covas DT, de Lucena Angulo I, Vianna Bonini Palma P, Zago MA.
    Haematologica; 2004 Mar; 89(3):273-80. PubMed ID: 15020264
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  • 25. Effects of hydroxyurea on hemoglobin F and water content in the red blood cells of dogs and of patients with sickle cell anemia.
    Orringer EP, Blythe DS, Johnson AE, Phillips G, Dover GJ, Parker JC.
    Blood; 1991 Jul 01; 78(1):212-6. PubMed ID: 1712641
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  • 26. Plasma and urine hydroxyurea levels might be useful in the management of adult sickle cell disease.
    Bachir D, Hulin A, Huet E, Habibi A, Nzouakou R, El Mahrab M, Astier A, Galacteros F.
    Hemoglobin; 2007 Jul 01; 31(4):417-25. PubMed ID: 17994375
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  • 28. Hematologic response to hydroxyurea therapy in children with beta-thalassemia major.
    Mtvarelidze Z, Kvezereli-Kopadze A, Kvezereli-Kopadze M, Mestiashvili I.
    Georgian Med News; 2008 Mar 01; (156):91-4. PubMed ID: 18403819
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  • 31. Hemoglobin switch in the newborn: a flow cytometry analysis.
    Amoyal I, Fibach E.
    Neonatology; 2007 Mar 01; 91(1):61-8. PubMed ID: 17344654
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  • 32. Evaluation of F cells in sickle cell disorders by flow cytometry -- comparison with the Kleihauer-Betke's slide method.
    Italia KY, Colah R, Mohanty D.
    Int J Lab Hematol; 2007 Dec 01; 29(6):409-14. PubMed ID: 17988294
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  • 33. Hydroxyurea (HU) for prevention of recurrent stroke in sickle cell anemia (SCA).
    Sumoza A, de Bisotti R, Sumoza D, Fairbanks V.
    Am J Hematol; 2002 Nov 01; 71(3):161-5. PubMed ID: 12410569
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  • 34. Hydroxyurea in the treatment of major beta-thalassemia and importance of genetic screening.
    Alebouyeh M, Moussavi F, Haddad-Deylami H, Vossough P.
    Ann Hematol; 2004 Jul 01; 83(7):430-3. PubMed ID: 14722738
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  • 35. [Bilateral ankle ulcers associated with hydroxyurea therapy for chronic myelogenous leukemia].
    Masuoka H, Kobayashi M, Kaito K, Yoshida M, Sekita T, Saeki A, Nishiwaki K, Shimada T, Ochiai S, Ootsubo H.
    Rinsho Ketsueki; 1995 Feb 01; 36(2):156-8. PubMed ID: 7715088
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  • 37. Molecular crowding limits the role of fetal hemoglobin in therapy for sickle cell disease.
    Rotter M, Aprelev A, Adachi K, Ferrone FA.
    J Mol Biol; 2005 Apr 15; 347(5):1015-23. PubMed ID: 15784260
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  • 38. Predicting the effectiveness of hydroxyurea in individual sickle cell anemia patients.
    Valafar H, Valafar F, Darvill A, Albersheim P, Kutlar A, Woods KF, Hardin J.
    Artif Intell Med; 2000 Feb 15; 18(2):133-48. PubMed ID: 10648847
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  • 39. Population pharmacokinetics and pharmacodynamics of hydroxyurea in sickle cell anemia patients, a basis for optimizing the dosing regimen.
    Paule I, Sassi H, Habibi A, Pham KP, Bachir D, Galactéros F, Girard P, Hulin A, Tod M.
    Orphanet J Rare Dis; 2011 May 28; 6():30. PubMed ID: 21619673
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