Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Fatou Guèye Tall"'
Autor:
El Hadji Malick Ndour, Khuthala Mnika, Fatou Guèye Tall, Moussa Seck, Indou Dème Ly, Victoria Nembaware, Gaston Kuzamunu Mazandu, Hélène Ange Thérèse Sagna Bassène, Rokhaya Dione, Aliou Abdoulaye Ndongo, Jean Pascal Demba Diop, Nènè Oumou Kesso Barry, Moustapha Djité, Rokhaya Ndiaye Diallo, Papa Madièye Guèye, Saliou Diop, Ibrahima Diagne, Aynina Cissé, Ambroise Wonkam, Philomène Lopez Sall
Publikováno v:
PLoS ONE, Vol 17, Iss 11, p e0273745 (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 sickling of red blood cells in small blood vessels which leads to a range of multiorgan com
Externí odkaz:
https://doaj.org/article/a1627c28a3d941218b51f24597e04dc2
Autor:
Moustapha Djite, Philomène Lopez Sall, Ambroise Wonkam, Aynina Cisse, Ibrahima Diagne, Saliou Diop, Papa Madièye Gueye, Rokhaya Ndiaye Diallo, Souleymane Aidara, Sokhna Mara, Younoussa Keita, Aïssatou Toure, El Hadji Malick Ndour, Nènè Oumou kesso Barry, Jean Pascal Demba Diop, Aliou Abdoulaye Ndongo, Hélène Ange Thérèse Sagna-Bassene, Victoria Nembaware, Indou Dème Ly, Moussa Seck, Khuthala Mnika, Gaston Kuzamunu Mazandu, Fatou Guèye Tall, Rokhaya Dione
Publikováno v:
International Journal of Biological and Chemical Sciences; Vol. 15 No. 6 (2021); 2283-2296
La détermination du Débit de Filtration Glomérulaire (DFG) est importante chez les drépanocytaires du fait qu’ils constituent un groupe de patients chez lesquels des atteintes rénales sont fréquemment décrites notamment l’hyperfiltration g
Autor:
Fatou Gueye Tall, Cyril Martin, El hadji Malick Ndour, Camille Faes, Indou Déme Ly, Vincent Pialoux, Philippe Connes, Papa Madieye Gueye, Rokhaya Ndiaye Diallo, Céline Renoux, Ibrahima Diagne, Pape Amadou Diop, Aynina Cissé, Philomène Lopez Sall, Philippe Joly
Publikováno v:
Antioxidants, Vol 9, Iss 9, p 863 (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, G6PD deficiency, HbF quantitative trait loci; QTL) and pro/antioxidant genes polymorphisms
Externí odkaz:
https://doaj.org/article/7d31a1249997430fb877d58cca12ad67