Nathalie Lemonne

发表

Blood Rheology: Key Parameters, Impact on Blood Flow, Role in Sickle Cell Disease and Effects of Exercise

Y. Bertrand, P. Joly, P. Connes, 2019, Front. Physiol..

Oxidative stress, inflammation, blood rheology, and microcirculation in adults with sickle cell disease: Effects of hydroxyurea treatment and impact of sickle cell syndrome

O. Hue, M. Billaud, P. Connes, 2021, European journal of haematology.

Exacerbation of oxidative stress during sickle vaso‐occlusive crisis is associated with decreased anti‐band 3 autoantibodies rate and increased red blood cell‐derived microparticle level: a prospective study

K. Charlot, P. Connes, B. Tressières, 2017, British journal of haematology.

Effects of Poloxamer 188 on red blood cell membrane properties in sickle cell anaemia

B. Le Pioufle, O. Français, P. Connes, 2016, British journal of haematology.

Substance use disorder of equimolar oxygen-nitrous oxide mixture in French sickle-cell patients: results of the PHEDRE study

N. Authier, M. Ruivard, N. Elenga, 2024, Orphanet journal of rare diseases.

Activation State of α4β1 Integrin on Sickle Red Blood Cells Is Linked to the Duffy Antigen Receptor for Chemokines (DARC) Expression*

J. Elion, J. Picot, W. El Nemer, 2010, The Journal of Biological Chemistry.

Haemolysis and abnormal haemorheology in sickle cell anaemia

O. Hue, S. Ballas, P. Connes, 2014, British journal of haematology.

Male Gender, Increased Blood Viscosity, Body Mass Index and Triglyceride Levels Are Independently Associated with Systemic Relative Hypertension in Sickle Cell Anemia

P. Connes, B. Tressières, M. Etienne‐Julan, 2013, PloS one.

Blood Thixotropy in Patients with Sickle Cell Anaemia: Role of Haematocrit and Red Blood Cell Rheological Properties

M. Billaud, P. Connes, M. Etienne‐Julan, 2014, PloS one.

Men with Sickle Cell Anemia and Priapism Exhibit Increased Hemolytic Rate, Decreased Red Blood Cell Deformability and Increased Red Blood Cell Aggregate Strength

J. Elion, M. Billaud, P. Connes, 2016, PloS one.

Red blood cell nitric oxide synthase activation is increased in patients with sickle cell hemoglobin C disease

W. Bloch, F. Suhr, P. Connes, 2015, American journal of hematology.

Lipid profiles in French West Indies sickle cell disease cohorts, and their general population

P. Connes, B. Tressières, M. Etienne‐Julan, 2018, Lipids in Health and Disease.

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.

Association Between Nitric Oxide, Oxidative Stress, Eryptosis, Red Blood Cell Microparticles, and Vascular Function in Sickle Cell Anemia

Y. Bertrand, P. Joly, P. Connes, 2020, Frontiers in Immunology.

Delayed beneficial effect of acute exercise on red blood cell aggregate strength in patients with sickle cell anemia.

O. Hue, S. Sinnapah, P. Connes, 2012, Clinical hemorheology and microcirculation.

High red blood cell nitric oxide synthase activation is not associated with improved vascular function and red blood cell deformability in sickle cell anaemia

K. Charlot, W. Bloch, F. Suhr, 2015, British journal of haematology.