Ex Vivo Complement Activation on Endothelial Cells: Research and Translational Value

Complement activation in sickle cell disease: Dependence on cell density, hemolysis and modulation by hydroxyurea therapy

(2020) Lubka T. Roumenina et al.   AMERICAN JOURNAL OF HEMATOLOGY

Complement as the enabler of carfilzomib‐induced thrombotic microangiopathy

(2020) Miquel Blasco et al.   BRITISH JOURNAL OF HAEMATOLOGY

An Ex Vivo Test of Complement Activation on Endothelium for Individualized Eculizumab Therapy in Hemolytic Uremic Syndrome

(2019) Miriam Galbusera et al.   AMERICAN JOURNAL OF KIDNEY DISEASES

Complement Activation and Thrombotic Microangiopathies

(2019) Marta Palomo et al.   Clinical Journal of the American Society of Nephrology

Complement activation and regulation in rheumatic disease

(2019) Douwe J. Dijkstra et al.   SEMINARS IN IMMUNOLOGY

C5b9 Formation on Endothelial Cells Reflects Complement Defects among Patients with Renal Thrombotic Microangiopathy and Severe Hypertension

(2018) Sjoerd A.M.E.G. Timmermans et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Heme Drives Susceptibility of Glomerular Endothelium to Complement Overactivation Due to Inefficient Upregulation of Heme Oxygenase-1

(2018) Olivia May et al.   Frontiers in Immunology

Modified Ham test for atypical hemolytic uremic syndrome

(2015) E. Gavriilaki et al.   BLOOD

Functional Characterization of Autoantibodies against Complement Component C3 in Patients with Lupus Nephritis

(2015) Vasil V. Vasilev et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Complement System Part II: Role in Immunity

(2015) Nicolas S. Merle et al.   Frontiers in Immunology

Dynamics of complement activation in aHUS and how to monitor eculizumab therapy

(2014) M. Noris et al.   BLOOD

Complement activation by heme as a secondary hit for atypical hemolytic uremic syndrome

(2013) M. Frimat et al.   BLOOD

A prevalent C3 mutation in aHUS patients causes a direct C3 convertase gain of function

(2012) L. T. Roumenina et al.   BLOOD

Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome

(2009) L. T. Roumenina et al.   BLOOD