Search Results - "Ndour, El Hadji Malick"
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Biomarkers of sickle cell nephropathy in Senegal
Published in PloS one (21-11-2022)“…Sickle cell anemia (SCA) is caused by a single point variation in the β-globin gene (HBB): c.20A> T (p.Glu7Val), in homozygous state. SCA is characterized by…”
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Biomarkers of sickle cell nephropathy in Senegal
Published in PloS one (21-11-2022)“…Sickle cell anemia (SCA) is caused by a single point variation in the β-globin gene (HBB): c.20A> T (p.Glu7Val), in homozygous state. SCA is characterized by…”
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Journal Article -
3
Combined and differential effects of alpha‐thalassemia and HbF‐quantitative trait loci in Senegalese hydroxyurea‐free children with sickle cell anemia
Published in Pediatric blood & cancer (01-10-2019)“…Background Our objective was to investigate the combined and differential effects of alpha‐thalassemia –3.7 kb deletion and HbF‐promoting quantitative trait…”
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A Metabolomic Signature of Ischemic Stroke Showing Acute Oxidative and Energetic Stress
Published in Antioxidants (01-01-2024)“…Metabolomics is a powerful data-driven tool for in-depth biological phenotyping that could help identify the specific metabolic profile of cryptogenic strokes,…”
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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
Published in Antioxidants (14-09-2020)“…Oxidative stress would play a role in the pathophysiology of sickle cell anemia (SCA). We tested the impact of common SCA genetic modifiers (alpha-thalassemia,…”
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Effects of Senegal haplotype ( Xmn1 -rs7412844), alpha-thalassemia (3.7kb HBA1/HBA2 deletion), NPRL3 -rs11248850 and BCL11A -rs4671393 variants on sickle cell nephropathy
Published in International journal of biochemistry and molecular biology (2022)“…Sickle cell anemia (SCA) can cause substantial kidney dysfunction resulting in sickle cell nephropathy, which may be affected by the presence of modifier…”
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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.Leu89Glufs2]
Published in Hemoglobin (04-03-2017)“…Sickle cell disease is a genetic disorder with a large variability in the pattern and severity of clinical manifestations. Different genetic modulators have…”
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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
Published in Antioxidants (01-09-2020)“…Oxidative stress would play a role in the pathophysiology of sickle cell anemia (SCA). We tested the impact of common SCA genetic modifiers (alpha-thalassemia,…”
Get full text
Journal Article