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Journal Abstract Search

263 related items for PubMed ID: 26961071

  • 21. Influence of βS-Globin Haplotypes and Hydroxyurea on Arginase I Levels in Sickle Cell Disease.
    Moreira JA, Machado RP, Laurentino MR, Lemes RP, Barbosa MC, Santos TE, Bandeira IC, Martins AM.
    Dis Markers; 2016; 2016():9172726. PubMed ID: 27274608
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  • 22. Relationship between oxidative stress, glutathione S-transferase polymorphisms and hydroxyurea treatment in sickle cell anemia.
    Silva DG, Belini Junior E, Torres Lde S, Ricci Júnior O, Lobo Cde C, Bonini-Domingos CR, de Almeida EA.
    Blood Cells Mol Dis; 2011 Jun 15; 47(1):23-8. PubMed ID: 21489839
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  • 23. Unusual β-Globin Haplotype Distribution in Newborns from Bengo, Angola.
    Borges E, Tchonhi C, Couto CSB, Gomes V, Amorim A, Prata MJ, Brito M.
    Hemoglobin; 2019 May 15; 43(3):149-154. PubMed ID: 31394941
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  • 25. Rearrangements of the beta-globin gene cluster in apparently typical betaS haplotypes.
    Zago MA, Silva WA, Gualandro S, Yokomizu IK, Araujo AG, Tavela MH, Gerard N, Krishnamoorthy R, Elion J.
    Haematologica; 2001 Feb 15; 86(2):142-5. PubMed ID: 11224482
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  • 26. Effect of alpha-thalassemia and beta-globin gene cluster haplotypes on the hematological and clinical features of sickle-cell anemia in Brazil.
    Figueiredo MS, Kerbauy J, Gonçalves MS, Arruda VR, Saad ST, Sonati MF, Stoming T, Costa FF.
    Am J Hematol; 1996 Oct 15; 53(2):72-6. PubMed ID: 8892730
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  • 30. 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 15; 34(3):262-6. PubMed ID: 22260316
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  • 31. Restriction mapping of βS locus among Tunisian sickle-cell patients.
    Imen M, Ikbel BM, Leila C, Fethi M, Amine Z, Mohamed B, Salem A.
    Am J Hum Biol; 2011 Jun 15; 23(6):815-9. PubMed ID: 21965081
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  • 32. Genotype-phenotype correlation of sickle cell disease in the United Arab Emirates.
    el-Kalla S, Baysal E.
    Pediatr Hematol Oncol; 1998 Jun 15; 15(3):237-42. PubMed ID: 9615321
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  • 34. DNA sequence variation in a negative control region 5' to the beta-globin gene correlates with the phenotypic expression of the beta s mutation.
    Elion J, Berg PE, Lapouméroulie C, Trabuchet G, Mittelman M, Krishnamoorthy R, Schechter AN, Labie D.
    Blood; 1992 Feb 01; 79(3):787-92. PubMed ID: 1346253
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  • 36. Beta-globin gene haplotypes among cameroonians and review of the global distribution: is there a case for a single sickle mutation origin in Africa?
    Bitoungui VJ, Pule GD, Hanchard N, Ngogang J, Wonkam A.
    OMICS; 2015 Mar 01; 19(3):171-9. PubMed ID: 25748438
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  • 38. 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 01; 49(6):3000605211019918. PubMed ID: 34187213
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  • 39. 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 01; 10(1):19-24. PubMed ID: 8913718
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  • 40. The co-inheritance of alpha-thalassemia and sickle cell anemia is associated with better hematological indices and lower consultations rate in Cameroonian patients and could improve their survival.
    Rumaney MB, Ngo Bitoungui VJ, Vorster AA, Ramesar R, Kengne AP, Ngogang J, Wonkam A.
    PLoS One; 2014 Apr 01; 9(6):e100516. PubMed ID: 24978191
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