Danielle Mougenel

Does increased red blood cell deformability raise the risk for osteonecrosis in sickle cell anemia?

P. Connes, M. Mukisi-Mukaza, B. Tressières, 2013, Blood.

Association between relative systemic hypertension and otologic disorders in patients with sickle cell‐hemoglobin C disorder

P. Connes, F. Lionnet, B. Tressières, 2014, American journal of hematology.

Alpha-thalassemia is associated with a decreased occurrence and a delayed age-at-onset of albuminuria in sickle cell anemia patients.

J. Elion, P. Connes, M. Romana, 2010, Blood cells, molecules & diseases.

Association between Duffy antigen receptor for chemokines expression and levels of inflammation markers in sickle cell anemia patients.

J. Elion, M. Mukisi-Mukaza, M. Romana, 2010, Clinical immunology.

Impaired blood rheology plays a role in the chronic disorders associated with sickle cell-hemoglobin C disease

P. Connes, F. Lionnet, B. Tressières, 2014, Haematologica.

Alpha thalassemia protects sickle cell anemia patients from macro-albuminuria through its effects on red blood cell rheological properties.

P. Connes, B. Tressières, M. Etienne‐Julan, 2014, Clinical hemorheology and microcirculation.

Does increased red blood cell deformability raise the risk for osteonecrosis in sickle cell anemia?

P. Connes, M. Mukisi-Mukaza, B. Tressières, 2013, Blood.