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Journal Abstract Search

409 related items for PubMed ID: 23620965

  • 21. [Hemoglobin beta S haplotype in the Kebili region (southern Tunisia)].
    Frikha M, Fakhfakh F, Mseddi S, Gargouri J, Ghali L, Labiadh Z, Harrabi M, Souissi T, Ayadi H.
    Transfus Clin Biol; 1998 Apr; 5(2):166-72. PubMed ID: 9618841
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  • 22. Phenotypic variation in sickle cell disease: the role of beta globin haplotype, alpha thalassemia, and fetal hemoglobin in HbSS.
    Serjeant GR.
    Expert Rev Hematol; 2022 Feb; 15(2):107-116. PubMed ID: 35143361
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  • 23. DNA haplotypes in Africans and West Indians with sickle cell anaemia or SC disease.
    Konstantopoulos K, Vulliamy T, Swirsky D, Reeves JD, Kaeda J, Luzzatto L.
    Gene Geogr; 1996 Apr; 10(1):19-24. PubMed ID: 8913718
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  • 24. Are there clinical phenotypes of homozygous sickle cell disease?
    Alexander N, Higgs D, Dover G, Serjeant GR.
    Br J Haematol; 2004 Aug; 126(4):606-11. PubMed ID: 15287956
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  • 26. 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; 100(4):921-931. PubMed ID: 33586016
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  • 27. The influence of uridine diphosphate glucuronosyl transferase 1A promoter polymorphisms, beta-globin gene haplotype, co-inherited alpha-thalassemia trait and Hb F on steady-state serum bilirubin levels in sickle cell anemia.
    Adekile A, Kutlar F, McKie K, Addington A, Elam D, Holley L, Clair B, Kutlar A.
    Eur J Haematol; 2005 Aug; 75(2):150-5. PubMed ID: 16004608
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  • 28. Beta s-gene-cluster haplotypes in sickle cell anemia. Clinical and hematologic features.
    Powars DR.
    Hematol Oncol Clin North Am; 1991 Jun; 5(3):475-93. PubMed ID: 1713910
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  • 30. Priapism and impotence in homozygous sickle cell disease.
    Emond AM, Holman R, Hayes RJ, Serjeant GR.
    Arch Intern Med; 1980 Nov; 140(11):1434-7. PubMed ID: 6159833
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  • 35. Molecular analysis of the β-globin gene cluster haplotypes in a Sudanese population with sickle cell anaemia.
    Elderdery AY, Mills J, Mohamed BA, Cooper AJ, Mohammed AO, Eltieb N, Old J.
    Int J Lab Hematol; 2012 Jun; 34(3):262-6. PubMed ID: 22260316
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  • 37. Frequency of beta S globin gene haplotypes among sickle cell patients in Nigeria.
    Adabale A, Makanjuola SBL, Akinbami A, Dosunmu A, Akanmu A, Javid FA, Ajonuma LC.
    J Int Med Res; 2021 Jun; 49(6):3000605211019918. PubMed ID: 34187213
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  • 38. Sickle cell anaemia in Nigeria: a comparison between Benin and Lagos.
    Akenzua G, Akinyanju O, Kulozik A, Whitehead S, Morris J, Serjeant BE, Serjeant G.
    Afr J Med Med Sci; 1994 Jun; 23(2):101-7. PubMed ID: 7542830
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  • 39. Hematologically and genetically distinct forms of sickle cell anemia in Africa. The Senegal type and the Benin type.
    Nagel RL, Fabry ME, Pagnier J, Zohoun I, Wajcman H, Baudin V, Labie D.
    N Engl J Med; 1985 Apr 04; 312(14):880-4. PubMed ID: 2579336
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  • 40. Acute splenic sequestration in female children with sickle cell disease in the North of Jordan.
    Al-Rimawi HS, Abdul-Qader M, Jallad MF, Amarin ZO.
    J Trop Pediatr; 2006 Dec 04; 52(6):416-20. PubMed ID: 16951418
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