Marie-Alice Macher

Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies

Aude Servais, Laure‐Hélène Noël, Lubka T. Roumenina et al. · Kidney International · 2012 · 567 citations

Medicine, Immunology, Nephrology +17

Anti–Factor H Autoantibodies Associated with Atypical Hemolytic Uremic Syndrome

Marie‐Agnès Dragon‐Durey, Chantal Loirat, Sylvie Cloarec et al. · Journal of the American Society of Nephrology · 2004 · 500 citations

Life Sciences, Hematology, Immunology +16

Differential Impact of Complement Mutations on Clinical Characteristics in Atypical Hemolytic Uremic Syndrome

Anne‐Laure Sellier‐Leclerc, Véronique Frémeaux‐Bacchi, Marie‐Agnès Dragon‐Durey et al. · Journal of the American Society of Nephrology · 2007 · 429 citations

Life Sciences, Genetics, Pediatrics +15

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

Lubka T. Roumenina, Mathieu Jablonski, Christophe Hue et al. · Blood · 2009 · 155 citations · Full text

Medicine, Immunology, Nephrology +12

Enhanced Expression of the CD71 Mesangial IgA1 Receptor in Berger Disease and Henoch-Schönlein Nephritis

Élie Haddad, Ivan Cruz Moura, Michelle Arcos‐Fajardo et al. · Journal of the American Society of Nephrology · 2003 · 104 citations

Medicine, Nephrology, Pathology +17