Association between plasma free haem and incidence of vaso-occlusive episodes and acute chest syndrome in children with sickle cell disease, British Journal of Haematology, vol.106, issue.5, pp.702-705, 2013. ,
DOI : 10.1111/bjh.12445
Enhancement of sickle erythrocyte adherence to endothelium by autologous platelets, American Journal of Hematology, vol.35, issue.1, pp.44-48, 1990. ,
DOI : 10.1002/ajh.2830340110
Membrane Peroxidation and Methemoglobin Formation Are Both Necessary for Band 3 Clustering: Mechanistic Insights into Human Erythrocyte Senescence, Biochemistry, vol.52, issue.34, pp.5760-5769, 2013. ,
DOI : 10.1021/bi400405p
Oxygen radical inhibition of nitric oxide-dependent vascular function in sickle cell disease, Proceeding of the National Academy of Sciences of the United States of America, pp.15215-15220, 2001. ,
DOI : 10.1073/pnas.221292098
Definitions of the phenotypic manifestations of sickle cell disease CURAMA study group Circulating erythrocyte-derived microparticles are associated with coagulation activation in sickle cell disease, Comprehensive Sickle Cell Centers. American Journal of Hematology Haematologica, vol.85, issue.94, pp.6-13, 2009. ,
Activated monocytes in sickle cell disease: potential role in the activation of vascular endothelium and vasoocclusion, Blood, vol.96, pp.2451-2459, 2000. ,
Non-transferrin bound iron: A key role in iron overload and iron toxicity, Biochimica et Biophysica Acta (BBA) - General Subjects, vol.1820, issue.3, pp.403-410, 2012. ,
DOI : 10.1016/j.bbagen.2011.07.014
URL : https://hal.archives-ouvertes.fr/hal-00739430
Circulating cell membrane microparticles transfer heme to endothelial cells and trigger vasoocclusions in sickle cell disease, Blood, vol.125, issue.24, pp.3805-3814, 2015. ,
DOI : 10.1182/blood-2014-07-589283
URL : https://hal.archives-ouvertes.fr/hal-01186628
Sickle Cell Vaso-Occlusion, Hematology/Oncology Clinics of North America, vol.19, issue.5, pp.771-784, 2005. ,
DOI : 10.1016/j.hoc.2005.08.002
Band 3 and glycophorin are progressively aggregated in density-fractionated sickle and normal red blood cells. Evidence from rotational and lateral mobility studies., Journal of Clinical Investigation, vol.91, issue.1, pp.208-217, 1993. ,
DOI : 10.1172/JCI116172
Cytoadherence-related neoantigens on Plasmodium falciparum (human malaria)-infected human erythrocytes result from the exposure of normally cryptic regions of the band 3 protein, Parasitology, vol.65, issue.03, pp.257-267, 1994. ,
DOI : 10.1073/pnas.86.23.9089
Maternal Plasma Fibronectin and Advanced Oxidative Protein Products for the Prediction of Preeclampsia in High Risk Pregnancies: A Prospective Cohort Study, Fetal Diagnosis and Therapy, vol.26, issue.4, pp.189-194, 2009. ,
DOI : 10.1159/000259317
Acute pain in children and adults with sickle cell disease: management in the absence of evidence-based guidelines, Current Opinion in Hematology, vol.16, issue.3, pp.173-178, 2009. ,
DOI : 10.1097/MOH.0b013e328329e167
Sickle Cell Vasoocclusion: Heterotypic, Multicellular Aggregations Driven by Leukocyte Adhesion, Microcirculation, vol.11, issue.2, pp.167-177, 2004. ,
DOI : 10.1080/mic.11.2.167.177
Erythrocyte NADPH oxidase activity modulated by Rac GTPases, PKC, and plasma cytokines contributes to oxidative stress in sickle cell disease, Erythrocyte NADPH oxidase activity modulated by Rac GTPases, PKC, and plasma cytokines contributes to oxidative stress in sickle cell disease, pp.2099-2107, 2013. ,
DOI : 10.1182/blood-2012-07-441188
The acceleration of the propagation phase of thrombin generation in patients with steady-state sickle cell disease is associated with circulating erythrocyte-derived microparticles, Thrombosis and Haemostasis, vol.107, issue.6, pp.1044-1052, 2012. ,
DOI : 10.1160/TH11-10-0689
Assessment of oxidative stress in patients with sickle cell disease: The glutathione system and the oxidant???antioxidant status, Blood Cells, Molecules, and Diseases, vol.46, issue.3, pp.220-225, 2011. ,
DOI : 10.1016/j.bcmd.2011.01.002
Abnormal Adherence of Sickle Erythrocytes to Cultured Vascular Endothelium, Journal of Clinical Investigation, vol.65, issue.1, pp.154-160, 1980. ,
DOI : 10.1172/JCI109646
Spontaneous oxygen radical generation by sickle erythrocytes., Journal of Clinical Investigation, vol.70, issue.6, pp.1253-1259, 1982. ,
DOI : 10.1172/JCI110724
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC370342
Effects of oxidative stress on red blood cell rheology in sickle cell patients, British Journal of Haematology, vol.87, issue.4, pp.601-606, 2014. ,
DOI : 10.1111/bjh.12912
Red cell PMVs, plasma membrane-derived vesicles calling out for standards, Biochemical and Biophysical Research Communications, vol.399, issue.4, pp.465-469, 2010. ,
DOI : 10.1016/j.bbrc.2010.07.095
Adhesion of normal and sickle erythrocytes to endothelial monolayer cultures, Blood, vol.54, pp.872-876, 1979. ,
Care of the child with sickle cell disease: acute complications, Pediatric Nursing, vol.26, pp.373-379, 2000. ,
Clinical significance of circulating blood and endothelial cell microparticles in sickle-cell disease, Journal of Thrombosis and Thrombolysis, vol.14, issue.1, pp.167-175, 2014. ,
DOI : 10.1007/s11239-013-1028-3
Hypoxia/reoxygenation causes inflammatory response in transgenic sickle mice but not in normal mice, Journal of Clinical Investigation, vol.106, issue.3, pp.411-420, 2000. ,
DOI : 10.1172/JCI9225
Senescent sickle erythrocytes and endothelial adhesion via band 3 peptides, Journal of Blood Disorders & Transfusion, vol.4, pp.159-160, 2013. ,
Hemorheological risk factors of acute chest syndrome and painful vaso-occlusive crisis in children with sickle cell disease, Haematologica, vol.97, issue.11, pp.1641-1647, 2012. ,
DOI : 10.3324/haematol.2012.066670
URL : https://hal.archives-ouvertes.fr/inserm-00849038
Does IV Iron Induce Plasma Oxidative Stress in Critically Ill Patients? A Comparison With Healthy Volunteers*, Critical Care Medicine, vol.44, issue.3, pp.521-530, 2016. ,
DOI : 10.1097/CCM.0000000000001420
Naturally Occurring Anti-Band 3 Antibodies in Clearance of Senescent and Oxidatively Stressed Human Red Blood Cells, Transfusion Medicine and Hemotherapy, vol.39, issue.5, pp.321-327, 2012. ,
DOI : 10.1159/000342171
Caspase 3-mediated Proteolysis of the N-terminal Cytoplasmic Domain of the Human Erythroid Anion Exchanger 1 (Band 3), Journal of Biological Chemistry, vol.278, issue.52, pp.52551-52558, 2003. ,
DOI : 10.1074/jbc.M306914200
Peroxynitrite induces senescence and apoptosis of red blood cells through the activation of aspartyl and cysteinyl proteases, The FASEB Journal, vol.19, pp.416-418, 2005. ,
DOI : 10.1096/fj.04-2450fje
Clearance of oxidized erythrocytes by macrophages: Involvement of caspases in the generation of clearance signal at band 3 glycoprotein, Biochemical and Biophysical Research Communications, vol.363, issue.1, pp.57-62, 2007. ,
DOI : 10.1016/j.bbrc.2007.08.089
Fetal hemoglobin and hydroxycarbamide moduate both plasma concentration and cellular origin of circulating microparticles in sickle cell anemia children, Haematologica, vol.98, issue.6, pp.862-867, 2013. ,
DOI : 10.3324/haematol.2012.073619
Plasma Concentration of Platelet-Derived Microparticles Is Related to Painful Vaso-Occlusive Phenotype Severity in Sickle Cell Anemia, PLoS ONE, vol.21, issue.1, p.87243, 2014. ,
DOI : 10.1371/journal.pone.0087243.t001
Cellular origin and procoagulant properties of microparticles in meningococcal sepsis, Blood, vol.95, pp.930-935, 2000. ,
A phase 3 study of L-glutamine therapy for sickle cell anemia and sickle cell b 0 -thalassemia, Blood, vol.124, p.86, 2014. ,
Plasma levels of advanced glycation end products are associated with haemolysis-related organ complications in sickle cell patients, British Journal of Haematology, vol.277, issue.Pt 2, pp.62-69, 2010. ,
DOI : 10.1111/j.1365-2141.2010.08320.x
Oxidative stress in sickle cell disease; pathophysiology and potential implications for disease management, American Journal of Hematology, vol.104, issue.Suppl 1, pp.484-489, 2011. ,
DOI : 10.1002/ajh.22012
Oxidized and poorly glycosylated band 3 is selectively phosphorylated by Syk kinase to form large membrane clusters in normal and G6PD-deficient red blood cells, Biochemical Journal, vol.418, issue.2, pp.359-367, 2009. ,
DOI : 10.1042/BJ20081557
Sickle cell anemia as an inflammatory disease, Journal of Clinical Investigation, vol.106, issue.3, pp.337-338, 2000. ,
DOI : 10.1172/JCI10726
Mechanisms of plasma non-transferrin bound iron generation: insights from comparing transfused diamond blackfan anaemia with sickle cell and thalassaemia patients, British Journal of Haematology, vol.106, issue.5, pp.692-696, 2014. ,
DOI : 10.1111/bjh.13081
Automated assay for non-transferrin-bound iron in serum samples, Clinical Chemistry and Laboratory Medicine, vol.48, issue.10, pp.1427-1432, 2010. ,
DOI : 10.1515/CCLM.2010.287
Cell-free hemoglobin limits nitric oxide bioavailability in sickle-cell disease, Nature Medicine, vol.32, issue.12, pp.1383-1389, 2002. ,
DOI : 10.1074/jbc.M203236200
Hemoglobin Redox Reactions and Red Blood Cell Aging, Antioxidants & Redox Signaling, vol.18, issue.17, pp.2274-2283, 2013. ,
DOI : 10.1089/ars.2012.4867
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3638511
Plasmodium falciparum gametocyte adhesion to C32 cells via CD36 is inhibited by antibodies to modified band 3, Infection and Immunity, vol.64, pp.4261-4268, 1996. ,
Red Blood Cell Microparticles: Clinical Relevance, Transfusion Medicine and Hemotherapy, vol.39, issue.5, pp.342-347, 2012. ,
DOI : 10.1159/000342228
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3678264
Co-clustering of denatured hemoglobin with band 3: its role in binding of autoantibodies against band 3 to abnormal and aged erythrocytes, Proceeding of the National Academy of Sciences of the United States of America, pp.6137-6141, 1986. ,
Sickle blood contains tissue factor-positive microparticles derived from endothelial cells and monocytes, Blood, vol.102, issue.7, pp.2678-2683, 2003. ,
DOI : 10.1182/blood-2003-03-0693
A simple method for clinical assay of superoxide dismutase, Clinical Chemistry, vol.34, pp.497-500, 1988. ,
Band 3 peptides block the adherence of sickle cells to endothelial cells in vitro, Plasma annexin A5 and microparticle phosphatidylserine levels are elevated in sickle cell disease and increase further during painful crisis. Biochemical and Biophysical Research Communication, pp.4172-4179, 1997. ,
Not simply misshapen red cells: multimolecular and cellular events in sickle vaso-occlusion, Journal of Clinical Investigation, vol.124, issue.4, pp.1462-1465, 2014. ,
DOI : 10.1172/JCI75238
Acute chest syndrome in sickle cell disease: clinical presentation and course. Cooperative Study of Sickle Cell Disease, Blood, vol.89, pp.1787-1792, 1997. ,
Natural antiband 3 antibodies in patients with sickle cell disease, Comptes Rendus Biologies, vol.336, issue.3, pp.173-176 ,
DOI : 10.1016/j.crvi.2012.09.002
Advanced oxidation protein products as a novel marker of oxidative stress in uremia, Kidney International, vol.49, issue.5, pp.1304-1313, 1996. ,
DOI : 10.1038/ki.1996.186
Endothelial cell NADPH oxidase mediates the cerebral microvascular dysfunction in sickle cell transgenic mice, The FASEB Journal, vol.19, pp.989-991, 2005. ,
DOI : 10.1096/fj.04-3218fje
Platelet activation and platelet-erythrocyte aggregates in patients with sickle cell anemia, Journal of Laboratory and Clinical Medicine, vol.129, issue.5, pp.507-516, 1997. ,
DOI : 10.1016/S0022-2143(97)90005-6
Inhibition of myeloperoxidase decreases vascular oxidative stress and increases vasodilatation in sickle cell disease mice, The Journal of Lipid Research, vol.54, issue.11, pp.3009-3015, 2013. ,
DOI : 10.1194/jlr.M038281