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Journal Abstract Search

209 related items for PubMed ID: 33216016

  • 1. HbF-promoting polymorphisms may specifically reduce the residual risk of cerebral vasculopathy in SCA children with alpha-thalassemia.
    Joly P, Bonello-Palot N, Badens C, Pissard S, Chamouine A, Bernaudin F, Bertrand Y, Connes P, Renoux C.
    Clin Hemorheol Microcirc; 2021; 77(3):267-272. PubMed ID: 33216016
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  • 3. The XmnI (G)gamma polymorphism influences hemoglobin F synthesis contrary to BCL11A and HBS1L-MYB SNPs in a cohort of 57 beta-thalassemia intermedia patients.
    Nguyen TK, Joly P, Bardel C, Moulsma M, Bonello-Palot N, Francina A.
    Blood Cells Mol Dis; 2010 Aug 15; 45(2):124-7. PubMed ID: 20472475
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  • 5. DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease.
    Lettre G, Sankaran VG, Bezerra MA, Araújo AS, Uda M, Sanna S, Cao A, Schlessinger D, Costa FF, Hirschhorn JN, Orkin SH.
    Proc Natl Acad Sci U S A; 2008 Aug 19; 105(33):11869-74. PubMed ID: 18667698
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  • 7. Genetic Modifiers of Sickle Cell Disease: A Genotype-Phenotype Relationship Study in a Cohort of 82 Children on Mayotte Island.
    Muszlak M, Pissard S, Badens C, Chamouine A, Maillard O, Thuret I.
    Hemoglobin; 2015 Aug 19; 39(3):156-61. PubMed ID: 25806420
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  • 9. Existence of HbF Enhancer Haplotypes at HBS1L-MYB Intergenic Region in Transfusion-Dependent Saudi β-Thalassemia Patients.
    Cyrus C, Vatte C, Borgio JF, Al-Rubaish A, Chathoth S, Nasserullah ZA, Jarrash SA, Sulaiman A, Qutub H, Alsaleem H, Alzahrani AJ, Steinberg MH, Ali AK.
    Biomed Res Int; 2017 Aug 19; 2017():1972429. PubMed ID: 28280727
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  • 10. DNA polymorphisms at BCL11A, HBS1L-MYB and Xmn1-HBG2 site loci associated with fetal hemoglobin levels in sickle cell anemia patients from Northern Brazil.
    Cardoso GL, Diniz IG, Silva AN, Cunha DA, Silva Junior JS, Uchôa CT, Santos SE, Trindade SM, Cardoso Mdo S, Guerreiro JF.
    Blood Cells Mol Dis; 2014 Dec 19; 53(4):176-9. PubMed ID: 25084696
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  • 11. Rheological properties of sickle erythrocytes in patients with sickle-cell anemia: The effect of hydroxyurea, fetal hemoglobin, and α-thalassemia.
    Ballas SK, Connes P, Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia.
    Eur J Haematol; 2018 Dec 19; 101(6):798-803. PubMed ID: 30204261
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  • 13. rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients.
    Chaouch L, Moumni I, Ouragini H, Darragi I, Kalai M, Chaouachi D, Boudrigua I, Hafsia R, Abbes S.
    Hematology; 2016 Aug 19; 21(7):425-9. PubMed ID: 27077760
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  • 18. Genetic variants at HbF-modifier loci moderate anemia and leukocytosis in sickle cell disease in Tanzania.
    Mtatiro SN, Makani J, Mmbando B, Thein SL, Menzel S, Cox SE.
    Am J Hematol; 2015 Jan 19; 90(1):E1-4. PubMed ID: 25263325
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  • 20. The genetics of hemoglobin A2 regulation in sickle cell anemia.
    Griffin PJ, Sebastiani P, Edward H, Baldwin CT, Gladwin MT, Gordeuk VR, Chui DH, Steinberg MH.
    Am J Hematol; 2014 Nov 19; 89(11):1019-23. PubMed ID: 25042611
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