Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Indou Déme Ly"'
Autor:
Marica Rossi, Dapa Diallo, Aissata Tolo, Saliou Diop, Ibrahima Diagne, Suzanne Belinga, Robert Kitenge, Boidy Kouakou, Ismael Kamara, Youssouf Traore, Indou Deme Ly, Mor Diaw, Leon Tshilolo, Brigitte Ranque
Publikováno v:
HemaSphere, Vol 7, p e74149e5 (2023)
Externí odkaz:
https://doaj.org/article/29dec0d60e144871b869e78378afbf93
Autor:
Karina Tozatto-Maio, Robert Girot, Indou Deme Ly, Ana Cristina Silva Pinto, Vanderson Rocha, Francisco Fernandes, Ibrahima Diagne, Yahia Benzerara, Carla L. Dinardo, Julia Pavan Soler, Simone Kashima, Itauá Leston Araujo, Chantal Kenzey, Guilherme H. H. Fonseca, Evandra S. Rodrigues, Fernanda Volt, Luciana Jarduli, Annalisa Ruggeri, Christina Mariaselvam, Sandra F. M. Gualandro, Hanadi Rafii, Barbara Cappelli, Felipe Melo Nogueira, Graziana Maria Scigliuolo, Renato Luiz Guerino-Cunha, Kelen Cristina Ribeiro Malmegrim, Belinda P. Simões, Eliane Gluckman, Ryad Tamouza
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Sickle cell disease (SCD), the most common monogenic disease worldwide, is marked by a phenotypic variability that is, to date, only partially understood. Because inflammation plays a major role in SCD pathophysiology, we hypothesized that single nuc
Externí odkaz:
https://doaj.org/article/67cb8a7ed9504d0aaebc582eaf5a2b7d
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
Autor:
Babacar Niang, Amadou Lamine Fall, Idrissa Demba Ba, Younoussa Keita, Indou Déme Ly, Abou Ba, Aliou Thiongane, Aliou Abdoulaye Ndongo, Djibril Boiro, Lamine Thiam, Aissatou Ba, Morgiane Houngbadji, Mouhamed Fattah, Yaye Joor Djeng, Dieynaba Fafa Cissé, Idrissa Basse, Assane Sylla, Papa Moctar Faye, Saliou Diouf, Ousmane Ndiaye, Mamadou Sarr
Publikováno v:
The Pan African Medical Journal, Vol 25, Iss 46 (2016)
L'hypothyroïdie de l'enfant é été peu étudiée au Sénégal. Le but de cette étude était d'évaluer les aspects épidémiologiques, diagnostiques et évolutifs de l'hypothyroïdie congénitale. Il s'agissait d'une étude rétrospective descrip
Externí odkaz:
https://doaj.org/article/56526833e368444e8a3f4caf0feb60e9
Autor:
Aliou Thiongane, Aliou Abdoulaye Ndongo, Idrissa Demba Ba, Djibril Boiro, Papa Moctar Faye, Younoussa Keita, Aéssatou Ba, Djeynaba Fafa Cissé, Idrissa Basse, Lamine Thiam, Indou Déme Ly, Babacar Niang, Abou Ba, Amadou Lamine Fall, Saliou Diouf, Ousmane Ndiaye, Mamadou Ba, Mamadou Sarr
Publikováno v:
The Pan African Medical Journal, Vol 24, Iss 138 (2016)
Le syndrome hémolytique et urémique (SHU) est une cause fréquente d'insuffisance rénale aiguë (IRA) organique chez l'enfant. C'est une complication évolutive des gastroentérites aiguës (GEA) en particulier à Escherichia coli de l'enfant. Not
Externí odkaz:
https://doaj.org/article/5852cd2660104467b0fca22b6462f3b7
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:
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 (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/97f4c5efb8e842458e417b78f5558cc4
Publikováno v:
BMC Health Services Research, Vol 19, Iss 1, Pp 1-10 (2019)
Abstract Background Treatment of acute malnutrition in infants under 6 months is a relevant topic regarding the global problem of maternal and child malnutrition. While treatment for older age groups has shifted more towards an outpatient, community
Externí odkaz:
https://doaj.org/article/485f3c1b6e9c450ebc1357037542abbc
Autor:
Morgiane Solange Tognidé Sêlomin Houngbadji, Babacar Niang, Djibril Boiro, Aminata Mbaye, Abdoulaye Seck, Abdoulaye Aliou Ndongo, Indou Deme Ly, Ousmane Ndiaye
Publikováno v:
The Pan African Medical Journal, Vol 30, Iss 244 (2018)
Le syndrome de résistance à l'Adrénocorticotrophine Hormone (ACTH) est l'une des rares causes d'insuffisance surrénalienne chez l'enfant. Toutes les formes d'insensibilité héréditaire à l'ACTH décrites à ce jour sont d'origine autosomique r
Externí odkaz:
https://doaj.org/article/3c8546a80523449d963de6480bbb8c0e