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Journal Abstract Search

194 related items for PubMed ID: 6644841

  • 1. Splenic function in children with hemoglobin SC disease and sickle beta-thalassemia.
    Sills RH.
    J Natl Med Assoc; 1983 Oct; 75(10):991-4. PubMed ID: 6644841
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  • 3. Developmental pattern of splenic dysfunction in sickle cell disorders.
    Pearson HA, Gallagher D, Chilcote R, Sullivan E, Wilimas J, Espeland M, Ritchey AK.
    Pediatrics; 1985 Sep; 76(3):392-7. PubMed ID: 2412200
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  • 4. RBC surface pits in the sickle hemoglobinopathies.
    Sills RH, Oski FA.
    Am J Dis Child; 1979 May; 133(5):526-7. PubMed ID: 433877
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  • 5. The spleen in sickle cell disease and thalassemia.
    Powars DR, Pegelow CH.
    Am J Pediatr Hematol Oncol; 1979 May; 1(4):343-53. PubMed ID: 397779
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  • 6. Splenic functions in non-negro patients with sickle-cell anemia and sickle-cell beta thalassemia.
    Ozsoylu S, Altinöz N, Lâleli Y.
    Turk J Pediatr; 1979 May; 21(2-4):36-45. PubMed ID: 262062
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  • 7. 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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  • 8. Splenic function in sickle-cell diseases.
    Zago MA, Bottura C.
    Clin Sci (Lond); 1983 Sep 04; 65(3):297-302. PubMed ID: 6872464
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  • 11. [Sickle cell disease in the Netherlands].
    Statius van Eps LW.
    Ned Tijdschr Geneeskd; 1984 Jun 23; 128(25):1196-8. PubMed ID: 6462267
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  • 13. Bacteremia in children with sickle hemoglobin C disease and sickle beta(+)-thalassemia: is prophylactic penicillin necessary?
    Rogers ZR, Buchanan GR.
    J Pediatr; 1995 Sep 23; 127(3):348-54. PubMed ID: 7658261
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  • 14. The clinical pathophysiology of sickle cell disease.
    Embury SH.
    Annu Rev Med; 1986 Sep 23; 37():361-76. PubMed ID: 2423018
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  • 17. Functional asplenia in sickle-cell anemia.
    Pearson HA, Spencer RP, Cornelius EA.
    N Engl J Med; 1969 Oct 23; 281(17):923-6. PubMed ID: 5811425
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  • 18. Cholelithiasis in patients with major sickle hemoglobinopathies.
    Rennels MB, Dunne MG, Grossman NJ, Schwartz AD.
    Am J Dis Child; 1984 Jan 23; 138(1):66-7. PubMed ID: 6691315
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  • 20. Splenic function in Omani children with sickle cell disease: correlation with severity index, hemoglobin phenotype, iron status, and alpha-thalassemia trait.
    Wali YA, Al-Lamki Z, Hussein SS, Bererhi H, Kumar D, Wasifuddin S, Zachariah M, Ghosh K.
    Pediatr Hematol Oncol; 2002 Jan 23; 19(7):491-500. PubMed ID: 12217195
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