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Combined and differential effects of alpha-thalassemia and HbF-quantitative trait loci in Senegalese hydroxyurea-free children with sickle cell anemia.
Pediatr Blood Cancer. 2019 Oct;66(10):e27934. doi: 10.1002/pbc.27934. Epub 2019 Jul 19.
Pediatr Blood Cancer. 2019.
PMID: 31322815
Genetic Background of the Sickle Cell Disease Pediatric Population of Dakar, Senegal, and Characterization of a Novel Frameshift β-Thalassemia Mutation [HBB: c.265_266del; p.Leu89Glufs*2].
Gueye Tall F, Martin C, Malick Ndour EH, Déme Ly I, Renoux C, Chillotti L, Veyrenche N, Connes P, Madieye Gueye P, Ndiaye Diallo R, Lacan P, Diagne I, Amadou Diop P, Cissé A, Lopez Sall P, Joly P.
Gueye Tall F, et al. Among authors: amadou diop p.
Hemoglobin. 2017 Mar;41(2):89-95. doi: 10.1080/03630269.2017.1339610. Epub 2017 Jul 3.
Hemoglobin. 2017.
PMID: 28670947
Clinical Trial.
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Influence of Oxidative Stress Biomarkers and Genetic Polymorphisms on the Clinical Severity of Hydroxyurea-Free Senegalese Children with Sickle Cell Anemia.
Gueye Tall F, Martin C, Ndour EHM, Faes C, Déme Ly I, Pialoux V, Connes P, Gueye PM, Ndiaye Diallo R, Renoux C, Diagne I, Diop PA, Cissé A, Sall PL, Joly P.
Gueye Tall F, et al. Among authors: diop pa.
Antioxidants (Basel). 2020 Sep 14;9(9):863. doi: 10.3390/antiox9090863.
Antioxidants (Basel). 2020.
PMID: 32937882
Free PMC article.
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