M. Gueri and G. Serjeant, Leg ulcers in sickle-cell anaemia, Trop Geogr Med, vol.22, pp.155-160, 1970.

M. Koshy, R. Entsuah, A. Koranda, A. Kraus, and R. Johnson, Leg ulcers in patients with sickle cell disease, Blood, vol.74, pp.1403-1408, 1989.

K. Delaney, K. Axelrod, A. Buscetta, K. Hassell, and P. Adams-graves, Leg Ulcers in Sickle Cell Disease: Current Patterns and Practices, Hemoglobin, vol.17, issue.8, pp.325-332, 2013.
DOI : 10.1001/archderm.135.7.818

A. Bowers, H. Reid, A. Greenidge, C. Landis, and M. Reid, Blood Viscosity and the Expression of Inflammatory and Adhesion Markers in Homozygous Sickle Cell Disease Subjects with Chronic Leg Ulcers, PLoS ONE, vol.107, issue.7, pp.68929-23922670, 2013.
DOI : 10.1371/journal.pone.0068929.g005

J. Eckman, LEG ULCERS IN SICKLE CELL DISEASE, Hematology/Oncology Clinics of North America, vol.10, issue.6, pp.1333-134470404, 1996.
DOI : 10.1016/S0889-8588(05)70404-4

S. Giraldi, K. Abbage, L. Marinoni, V. Oliveira, and M. Pianowski, Leg Ulcer in Hereditary Spherocytosis, Pediatric Dermatology, vol.46, issue.5, pp.427-428, 2003.
DOI : 10.1046/j.1525-1470.2003.20512.x

V. Nolan, A. Adewoye, C. Baldwin, L. Wang, and Q. Ma, Sickle cell leg ulcers: associations with haemolysis and SNPs in Klotho, TEK and genes of the TGF-beta/BMP pathway, British Journal of Haematology, vol.19, issue.5, p.16681647, 2006.
DOI : 10.1097/01.ASN.0000093460.24823.5B

J. Taylor, V. Nolan, L. Mendelsohn, G. Kato, and M. Gladwin, Chronic Hyper-Hemolysis in Sickle Cell Anemia: Association of Vascular Complications and Mortality with Less Frequent Vasoocclusive Pain, PLoS ONE, vol.21, issue.5, 2008.
DOI : 10.1371/journal.pone.0002095.s005

V. Cumming, L. King, R. Fraser, G. Serjeant, and M. Reid, Venous incompetence, poverty and lactate dehydrogenase in Jamaica are important predictors of leg ulceration in sickle cell anaemia, British Journal of Haematology, vol.3, issue.1, pp.119-125, 2008.
DOI : 10.1097/00006534-196901000-00011

G. Kato, M. Gladwin, and M. Steinberg, Deconstructing sickle cell disease: Reappraisal of the role of hemolysis in the development of clinical subphenotypes, Blood Reviews, vol.21, issue.1, pp.37-47, 2007.
DOI : 10.1016/j.blre.2006.07.001

X. Waltz, M. Hardy-dessources, N. Lemonne, D. Mougenel, and M. Lalanne-mistrih, Is there a relationship between the hematocritto-viscosity ratio and microvascular oxygenation in brain and muscle? Clin Hemorheol Microcirc, 2013.

O. Baskurt and H. Meiselman, Erythrocyte aggregation: basic aspects and clinical importance, Clin Hemorheol Microcirc, vol.53, pp.23-37, 2013.

Y. Lamarre, M. Lalanne-mistrih, R. M. Lemonne, N. Mougenel, and D. , Male Gender, Increased Blood Viscosity, Body Mass Index and Triglyceride Levels Are Independently Associated with Systemic Relative Hypertension in Sickle Cell Anemia, PLoS ONE, vol.120, issue.6, pp.66004-23785465, 2013.
DOI : 10.1371/journal.pone.0066004.t003

URL : https://hal.archives-ouvertes.fr/inserm-00838991

N. Lemonne, Y. Lamarre, R. M. Mukisi-mukaza, M. Hardy-dessources, and M. , Does increased red blood cell deformability raise the risk for osteonecrosis in sickle cell anemia?, Blood, vol.121, issue.15, pp.3054-305610, 2013.
DOI : 10.1182/blood-2013-01-480277

URL : https://hal.archives-ouvertes.fr/inserm-00919490

S. Ballas, G. Dover, and S. Charache, Effect of hydroxyurea on the rheological properties of sickle erythrocytes in vivo, American Journal of Hematology, vol.310, issue.2, 1989.
DOI : 10.1002/ajh.2830320206

V. Tarer, M. Etienne-julan, J. Diara, M. Belloy, and M. Mukizi-mukaza, Sickle cell anemia in Guadeloupean children: pattern and prevalence of acute clinical events, European Journal of Haematology, vol.107, issue.3, pp.193-199, 2006.
DOI : 10.1111/j.1365-2141.2005.05411.x

A. Tan, T. Quah, P. Low, and S. Chong, A rapid and reliable 7-deletion multiplex polymerase chain reaction assay for alpha -thalassemia, Blood, vol.98, issue.1, pp.250-251, 2001.
DOI : 10.1182/blood.V98.1.250

L. Wang, R. Gill, T. Pedersen, L. Higgins, and J. Newman, Triglyceride-rich lipoprotein lipolysis releases neutral and oxidized FFAs that induce endothelial cell inflammation, The Journal of Lipid Research, vol.50, issue.2, pp.204-213, 2009.
DOI : 10.1194/jlr.M700505-JLR200

M. Nouraie, J. Lee, Y. Zhang, T. Kanias, and X. Zhao, The relationship between the severity of hemolysis, clinical manifestations and risk of death in 415 patients with sickle cell anemia in the US and Europe, Haematologica, vol.98, issue.3, pp.464-472, 2013.
DOI : 10.3324/haematol.2012.068965

O. Baskurt, M. Boynard, G. Cokelet, P. Connes, and B. Cooke, New guidelines for hemorheological laboratory techniques, Clin Hemorheol Microcirc, vol.42, pp.75-97, 2009.
URL : https://hal.archives-ouvertes.fr/hal-00709840

T. Alexy, E. Pais, J. Armstrong, H. Meiselman, and C. Johnson, Rheologic behavior of sickle and normal red blood cell mixtures in sickle plasma: implications for transfusion therapy, Transfusion, vol.72, issue.6, pp.912-918, 2006.
DOI : 10.1016/j.hoc.2005.07.002

J. Detterich, T. Alexy, M. Rabai, R. Wenby, and A. Dongelyan, Low-shear red blood cell oxygen transport effectiveness is adversely affected by transfusion and further worsened by deoxygenation in sickle cell disease patients on chronic transfusion therapy, Transfusion, vol.29, issue.2, p.22882132, 2013.
DOI : 10.1111/j.1537-2995.2012.03822.x

C. Minniti, J. Eckman, P. Sebastiani, M. Steinberg, and S. Ballas, Leg ulcers in sickle cell disease, American Journal of Hematology, vol.126, issue.10, pp.831-833, 2010.
DOI : 10.1002/ajh.21838

Y. Lamarre, R. M. Lemonne, N. Hardy-dessources, M. Tarer, and V. , Alpha thalassemia protects sickle cell anemia patients from macro-albuminuria through its effects on red blood cell rheological properties, Clin Hemorheol Microcirc, p.24004554, 2013.

C. Minniti, J. Taylor, M. Hildesheim, O. Neal, P. Wilson et al., Laboratory and echocardiography markers in sickle cell patients with leg ulcers, American Journal of Hematology, vol.86, issue.8, pp.705-708, 2011.
DOI : 10.1002/ajh.22065

O. Baskurt and H. Meiselman, Blood rheology and hemodynamics, Semin Thromb Hemost, vol.29, pp.435-450, 2003.

P. Bartolucci, C. Brugnara, A. Teixeira-pinto, S. Pissard, and K. Moradkhani, Erythrocyte density in sickle cell syndromes is associated with specific clinical manifestations and hemolysis, Blood, vol.120, issue.15, pp.3136-314110, 2012.
DOI : 10.1182/blood-2012-04-424184

URL : https://hal.archives-ouvertes.fr/inserm-00727759