Results 11 to 20 of about 1,433 (142)

Evaluation de la sensibilisation de la population contre la drépanocytose au Programme National de la Lutte Contre la Drépanocytose (PNLCD) en République Démocratique du Congo

Revue Congolaise des Sciences et Technologies
La drépanocytose demeure une pathologie héréditaire à fort impact sanitaire en République Démocratique du Congo, caractérisée par une morbidité et une mortalité élevée, particulièrement chez les enfants.
Bertin Mbenga Tampwo, Eric Panzi Kalunda, Daniel Twum, John Luhata, Pitchou Lukisa Kulembama, Jacques Emina, Ngianga Bakwin Kandala   +6 more
doaj   +3 more sources

Sickle cell anemia and pregnancy: Profile of hemodynamic changes in sickle cell pregnant women in Kinshasa

eJHaem, 2023
Pregnancy is accompanied by hormonal changes. These relate mainly to progesterone and placenate growth factor. Hemodynamic changes are also observed. in a sickle cell pregnant woman, all these changes have a direct effect on hypoxia.
Tite Minga Mikobi, Nelly Ciombo Kamuanya, Emmanuelle Ketsia Bokashanga Mikobi, Thérèse Ilunga Kalela, Pierre Zalagile Akilimali, Prosper Tshilobo Lukusa   +5 more
doaj   +2 more sources

De Koloci à la drépanocytose

Anthropologie & Santé, 2012
Sickle-cell disease affects 1-3% of newborns in sub-Saharan Africa. The epidemiological and anthropological situations as well as the unequal health policies from one country to another prove the interest for located historicized studies.
Agnès Lainé, Dapa Diallo, Bakary Traoré   +2 more
doaj   +3 more sources

Polygenic scores in the diagnosis of abnormal complete blood count values. [PDF]

Hemasphere
HemaSphere, Volume 10, Issue 6, June 2026.
Srour M, Lecluze E, Chacowry E, Saby M, Pincez T.   +4 more
europepmc   +2 more sources

Costs of Treating Uncomplicated Sickle Cell Complications in a Day Hospital Setting in Equatorial Africa. [PDF]

Anemia
Sickle cell disease (SCD) is a major public health concern in Africa. SCD healthcare expenses are covered by personal finances in the Congo due to the absence of universal public health insurance. Various strategies have been implemented to minimize this economic burden, including an outpatient management strategy. The present study evaluated the costs
Ngolet LO, Taylor J, de Chabervy Atipo A, Mikia CP, Bango C, Bantsimba FS, Ondzotto Ibatta I, Dokekias AE.   +7 more
europepmc   +2 more sources

Mitochondrial retention in mature red blood cells from patients with sickle cell disease is associated with stress erythropoiesis but not with proinflammatory state. [PDF]

Hemasphere
HemaSphere, Volume 8, Issue 11, November 2024.
Romana M, Laurance S, Hardy-Dessources MD, Claer L, Ravion S, Dorgham K, Garnier Y, Kuznicki L, Tarer V, Tressières B, Lefevre SD, Baccini V, Ostuni MA, Le Van Kim C, Etienne-Julan M.   +14 more
europepmc   +2 more sources

Genetic Contribution to Asthma Informs Acute Chest Syndrome Pathophysiology and Risk Stratification. [PDF]

Am J Hematol
ABSTRACT Acute chest syndrome (ACS) is a severe complication of sickle cell disease (SCD) occurring in ~50% of patients, some presenting frequent episodes. We lack tools to identify patients at high risk of ACS occurrence or frequent episodes. Epidemiological studies have found an association between asthma and ACS, but whether this link is causal is ...
El Aouhel S, Bellegarde V, Da Silva Faria S, St-Laurent T, Lecluze E, Pham Hung d'Alexandry d'Orengiani AL, Galactéros F, Bartolucci P, Legault MA, Lettre G, Pincez T.   +10 more
europepmc   +2 more sources

PI-09: LESSONS LEARNED FROM ONE DECADE EXPERIENCE OF THE « CENTRE DE RECHERCHE ET DE LUTTE CONTRE LA DRÉPANOCYTOSE (CRLD) » IN BAMAKO, MALI. [PDF]

Hemasphere, 2022
HemaSphere, Volume 6, Issue S4, Page 13-14, August 2022.
D. D, A. G.
europepmc   +2 more sources

Is chest X-ray still relevant for acute chest syndrome diagnosis? [PDF]

Health Sci Rep
Health Science Reports, Volume 7, Issue 5, May 2024.
Pelinski Y, Guindo A, Kassasseya C, Diallo D, Arlet JB, Mekontso Dessap A, Habibi A, Bartolucci P.   +7 more
europepmc   +2 more sources

Association of haemolysis markers, blood viscosity and microcirculation function with organ damage in sickle cell disease in sub‐Saharan Africa (the BIOCADRE study)

British Journal of Haematology, Volume 203, Issue 2, Page 319-326, October 2023., 2023
A case‐control study nested in the CADRE multinational African cohort was conducted in Bamako and Dakar in 235 patients with sickle cell anemia (SCA) to test multiple biological and functional markers as potential markers of six different SCA‐related chronic organ damage.
Brigitte Ranque, Mor Diaw, Abdoul Karim Dembele, Claudine Lapoumeroulie, Lucile Offredo, Oumar Tessougue, Serigne Mourtalla Gueye, Dapa Diallo, Saliou Diop, Yves Colin‐Aronovicz, Xavier Jouven, Olivier Blanc‐Brude, Pierre‐Louis Tharaux, Sylvain Le Jeune, Philippe Connes, Marc Romana, Caroline Le Van Kim   +16 more
wiley   +1 more source