Academic literature on the topic 'Hémoglobinopathie'
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Journal articles on the topic "Hémoglobinopathie"
Douma Maiga, Djibo, and Ibrahim Mahamane Gambo. "Niger : Évaluation de la dépendance iatrogène à la Codéine et au Tramadol chez les drépanocytaires." Psy Cause N° 78, no. 3 (April 5, 2019): 51–53. http://dx.doi.org/10.3917/psca.078.0053.
Full textElmachtani Idrissi, S., N. El Omri, R. El Jaoudi, A. Dami, S. Bouhsain, Z. Ouzzif, Y. Sekkach, et al. "Hémoglobinopathie O Arab homozygote dans une famille marocaine." Immuno-analyse & Biologie Spécialisée 27, no. 5 (October 2012): 268–71. http://dx.doi.org/10.1016/j.immbio.2012.05.002.
Full textBourée, Patrice, and Alireza Ensaf. "La drépanocytose : une hémoglobinopathie tropicale qui devient cosmopolite." Option/Bio 23, no. 481 (November 2012): 15–17. http://dx.doi.org/10.1016/s0992-5945(12)71113-3.
Full textKakpovi, K., E. Fianyo, NTA Oloude, KS Sossou, DAE Akolly, VES Koffi-Tessio, P. Houzou, et al. "Profil épidémiologique des affections rhumatismales des enfants en consultation rhumatologique à Lomé (Togo)." Rhumatologie Africaine Francophone 2, no. 1 (October 8, 2022): 7–13. http://dx.doi.org/10.62455/raf.v2i1.13.
Full textRhondali, O., A. Pouyau, C. Bonnard, and D. Chassard. "Comment je prends en charge un enfant qui souffre d’une hémoglobinopathie." Annales Françaises d'Anesthésie et de Réanimation 32, no. 12 (December 2013): e193-e197. http://dx.doi.org/10.1016/j.annfar.2013.10.005.
Full textKoffi-Tessio, VES, K. Kakpovi, E. Fianyo, O. Oniankitan, and M. Mijiyawa. "Goutte tophacée chez une togolaise de 56 ans porteuse d’une hémoglobinopathie CC." Rhumatologie Africaine Francophone 3, no. 1 (October 12, 2022): 30–32. http://dx.doi.org/10.62455/raf.v3i1.28.
Full textGirot, R., and L. Mandelbrot. "Le nouveau-né de mère atteinte d’une hémoglobinopathie majeure (thalassémie ou drépanocytose)." Archives de Pédiatrie 20, no. 5 (May 2013): H31—H32. http://dx.doi.org/10.1016/s0929-693x(13)71306-x.
Full textAndriuta, D., M. Assénova, A. Elinani, and M. Logak. "Une compression médullaire par hématopoïèse ectopique associée à une Hémoglobinopathie de Lepore." Revue Neurologique 169, no. 3 (March 2013): 277–78. http://dx.doi.org/10.1016/j.neurol.2012.09.007.
Full textMammeri, A., A. Djenouni, K. Amoura, A. Touaref, I. Frigaa, I. Kerkoub, and M. Laouar. "HEP-16 - Particularité de la prise en charge de l’hépatite C chez les patients avec hémoglobinopathie." Médecine et Maladies Infectieuses 46, no. 4 (June 2016): 55–56. http://dx.doi.org/10.1016/s0399-077x(16)30393-6.
Full textMasengo, Colette, and Jean-Paul Ngbolua. "Evaluation in silico de l’activité anti-drépanocytaire de quelques composés de l’huile essentielle de Lippia multiflora Moldenke (Verbenaceae)." Revue Congolaise des Sciences & Technologies 2, no. 3 (February 1, 2022): 424–29. http://dx.doi.org/10.59228/rcst.023.v2.i3.47.
Full textDissertations / Theses on the topic "Hémoglobinopathie"
Dachary, Martine. "Etude d'une hémoglobinopathie : l'hémoglobine SETIF." Paris 5, 1994. http://www.theses.fr/1994PA05P055.
Full textLeluan, Philippe. "Etude d'une hémoglobinopathie : association hémoglobine S/hémoglobine Korle Bu." Paris 5, 1992. http://www.theses.fr/1992PA05P184.
Full textTanoh, Laure. "Hémoglobinopathies et grossesse." Bordeaux 2, 1996. http://www.theses.fr/1996BOR2M002.
Full textChami, Ibtissam. "Contribution à l'étude du polymorphisme génétique des hémoglobines humaines et du mécanisme de l'induction par l'hydroxyurée du gène gamma de globine chez les patients drépanocytaires." Paris 12, 1998. http://www.theses.fr/1998PA120069.
Full textCousin, Bruno. "Hémoglobinopathies : étude bibliographique, stratégies de détection, exploitation de résultats d'électrophorèses de l'hémoglobine." Paris 5, 1989. http://www.theses.fr/1989PA05P088.
Full textBrun, Manuel. "Effets cellulaires et moléculaires de l'hydroxyurée sur les cellules endothéliales humaines en culture." Antilles-Guyane, 2004. http://www.theses.fr/2004AGUY0110.
Full textSince 1995,administration of hydroxyurea(HU) to sickle cell patients allows to reduce vaso occlusive crisis frequency and to decrease incidence of some of the main complications of that disease. However,its mechanism of action remains to be elucidade. In this contex,our goal is to study the effects of HU on the endothelium. A targeted study on candidates genes associated to an transcriptome analysis approach (on 406 human genes),has demonstrated the capacity of HU in human endothelial cells in culture to:decrease the synthesis of a vaconstrictor factor (endothelin-1),increase the expression of pro inflammatory factors such as ICAM-1,il-8 and the chemokine RANTES. Involvement of the soluble guanylate cyclase and the NFKB pathways in over expression of RANTES and IL-8 has been suggested by the use of specific inhibitors. In addition ,modulation of ICAM-1(a major endothelial receptor of Plasmodium Falciparum parasited red blood cells) by HU suggested the need of study in the field of paludous infection ,indeed, since sickle cell dasease (SCD) and malaria endemic areas are largely overlapping,any utilisation of that drug in this area should be preceded of safety studies. Hence,using an murine model of neuromalaria,we showed that administration of HU significantly recuded the mortality of treated mice. Finally ,this work demonstrates that endothelium is a target of HU. The above mentioned results also opens new therapeutic avenues in the field of SCD and malaria treatment
Diakité, Séidina Aboubacar Samba. "Polymorphismes érythrocytaires et protections contre le paludisme a Plasmodium falciparum : exploration de mécanismes innés." Thesis, Paris 6, 2015. http://www.theses.fr/2015PA066671/document.
Full textThe high prevalence of several inherited hemoglobin disorders, namely sickle cell trait (HbAS), HbAC and α-thalassemia, in malaria endemic areas is thought to be the consequence of their protective effects against malaria life-threatening manifestations. Numerous potential mechanisms have been proposed to explain this protective effect although many of them are not fully consistent with all available epidemiologic and clinical data. The first part of this thesis work explored the reduction of cytoadherence of infected RBC as a potential common mechanism for α-thalassemia-, HbAS- and HbAC-induced protection against malaria. To further explore this mechanism, and determine whether HbAS and HbAC select and maintain virulent P. falciparum parasite in nature, we compared the cytoadherence phenotype of P. falciparum isolates obtained from HbAS/HbAC and controls HbAA patients. The second part of the thesis work addressed the influence of HbAS on the deformability of uninfected RBC as well as the splenic retention of both uninfected RBCs and ring-infected RBCs. We observed a reduced adherence of α-thalassemic infected RBCs to human micro-vascular endothelial cells and monocytes compared to controls HbAA infected RBCs. The reduction was correlated to the number of non functional α- gene. Expression of PfEMP-1 on the surface of α- thalassemic infected RBCs was lower than on the surface of HbAA infected RBCs. There was no statistically significant difference between the cytoadherence of P. falciparum isolates obtained either from HbAS/HbAC or control HbAA malaria patients. The deformability of uninfected HbAS RBCs was slightly but significant lower than that of control uninfected HbAA RBCs. Retention rates of ring-infected HbAS and HbAA RBCs were similar either in human isolated spleen perfusion ex vivo and in microsphilters in vitro regardless of the oxygenation level. We did not observe any enhanced sickling of ring-infected RBCs compared to non infected RBCs, both in HbAS and HbSS samples. Based on these results along with available epidemiologic and previous experimental data, we propose a common malaria-protective mechanism of HbAS, HbAC and α-thalassemia whereby these hemoglobin disorders reduce the cytoadherence of mature P. falciparum-infected RBCs that stay in circulation where they are exposed to an enhanced splenic retention. These 2 mechanisms would act in conjunction to slower the rise of parasites loads in infected patients and protect them from sequestration-related complications of malaria
Pissard, Serge. "Contribution à l'étude de la régulation des gènes de globines : clonage et études de deux régions régulatrices." Paris 12, 1996. http://www.theses.fr/1996PA120076.
Full textM'Rad, Amel. "Contribution à l'étude des hémoglobines anormales : épidémiologie, structure, fonction des hémoglobines anormales en Tunisie." Paris 12, 1993. http://www.theses.fr/1993PA120051.
Full textCoulibaly, Foungotin Hamidou. "Étude des globules rouges par interférométrie ultrasonore : application à la rhéologie sanguine, à l'immuno-hématologie et aux hémoglobinopathies." Paris 12, 1995. http://www.theses.fr/1995PA120063.
Full textBook chapters on the topic "Hémoglobinopathie"
Cabrol, D., and F. Goffinet. "Hémoglobinopathies." In Protocoles cliniques en obstétrique, 115–19. Elsevier, 2009. http://dx.doi.org/10.1016/b978-2-294-70236-5.00033-4.
Full textGoffinet, F., O. Anselem, M. Barrois, A. Girault, G. Grangé, J. Lepercq, C. Le Ray, E. Pannier, A. Theau, and V. Tsatsaris. "Hémoglobinopathies." In Protocoles Cliniques de Port-Royal en Obstétrique, 169–73. Elsevier, 2023. http://dx.doi.org/10.1016/b978-2-294-78205-3.00032-7.
Full textAya, G., D. Benhamou, F. Bolandard, M. Bonnin, E. Boselli, F. Broisin, B. Bryssine, et al. "Hémoglobinopathies peu ou asymptomatiques." In Protocoles en anesthésie et analgésie obstétricales, 23–24. Elsevier, 2010. http://dx.doi.org/10.1016/b978-2-294-71053-7.00008-1.
Full textAya, G., F. Bayoumeu, D. Benhamou, F. Bolandard, M. P. Bonnet, M. Bonnin, E. Boselli, et al. "Hémoglobinopathies peu ou asymptomatiques." In Protocoles en Anesthésie et Analgésie Obstétricales, 31–32. Elsevier, 2018. http://dx.doi.org/10.1016/b978-2-294-76011-2.00008-7.
Full textAucourt, J., E. Spas-Defasque, and A. Cotten. "Hémoglobinopathies et autres anémies." In Imagerie Musculosquelettique : Pathologies Générales, 713–30. Elsevier, 2013. http://dx.doi.org/10.1016/b978-2-294-71924-0.00022-x.
Full textAya, G., D. Benhamou, M. P. Bonnet, M. Bonnin, L. Bouvet, M. Bruyère, A. Castel, et al. "Hémoglobinopathies peu ou asymptomatiques." In Protocoles en Anesthésie et Analgésie Obstétricales, 26–27. Elsevier, 2021. http://dx.doi.org/10.1016/b978-2-294-77362-4.00008-7.
Full textChassard, Dominique. "Hémoglobinopathies peu ou asymptomatiques." In Protocoles en Anesthésie et Analgésie Obstétricales, 21–22. Elsevier, 2024. http://dx.doi.org/10.1016/b978-2-294-78414-9.00007-7.
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