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Kidney International|April 16, 2019
Atypical and secondary hemolytic uremic syndromes have a distinct presentation and no common genetic risk factorsAlice Le Clech, Noémie Simon-Tillaux, François Provôt, et al.
Transplantation|July 28, 2015
An Early Viral Response Predicts the Virological Response to Ribavirin in Hepatitis E Virus Organ Transplant PatientsNassim Kamar, Sebastien Lhomme, Florence Abravanel, et al.
Blood|January 11, 2017
Treatment of B-cell disorder improves renal outcome of patients with monoclonal gammopathy-associated C3 glomerulopathySophie Chauvet, Véronique Frémeaux-Bacchi, Florent Petitprez, et al.
The Journal of Rheumatology|January 3, 2017
Lupus Myocarditis: Initial Presentation and Longterm Outcomes in a Multicentric Series of 29 PatientsGuillemette Thomas, Fleur Cohen Aubart, Laurent Chiche, et al.
Blood|July 9, 2009
Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndromeLubka T Roumenina, Mathieu Jablonski, Christophe Hue, et al.
RMD Open|January 22, 2026
Impact of ANCA specificity on risk of cardiovascular events and death in ANCA-associated vasculitisJon Idoate Lacasia, Morgane Mourguet, Thomas Villeneuve, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|February 26, 2022
Complement Activation and Thrombotic Microangiopathy Associated With Monoclonal Gammopathy: A National French Case SeriesManon Martins, Frank Bridoux, Jean Michel Goujon, et al.
Kidney International|June 25, 2022
Results from a nationwide retrospective cohort measure the impact of C3 and soluble C5b-9 levels on kidney outcomes in C3 glomerulopathySophie Chauvet, Jill J Hauer, Florent Petitprez, et al.
Emerging Infectious Diseases|June 21, 2021
Shiga Toxin-Associated Hemolytic Uremic Syndrome in Adults, France, 2009-2017Benoît Travert, Antoine Dossier, Matthieu Jamme, et al.
Clinical Journal of the American Society of Nephrology : CJASN|August 24, 2023
Rare Variants in Complement Gene in C3 Glomerulopathy and Immunoglobulin-Mediated Membranoproliferative GNMarie Sophie Meuleman, Paula Vieira-Martins, Carine El Sissy, et al.
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