François Provôt

Genetics and Outcome of Atypical Hemolytic Uremic Syndrome

Véronique Frémeaux‐Bacchi, Fádi Fakhouri, Arnaud Garnier et al. · Clinical Journal of the American Society of Nephrology · 2013 · 713 citations

Life Sciences, Genetics, Nephrology +16

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

Pregnancy-Associated Hemolytic Uremic Syndrome Revisited in the Era of Complement Gene Mutations

Fádi Fakhouri, Lubka T. Roumenina, François Provôt et al. · Journal of the American Society of Nephrology · 2010 · 464 citations

Life Sciences, Genetics, Hematology +14

Epidemiology and pathophysiology of adulthood-onset thrombotic microangiopathy with severe ADAMTS13 deficiency (thrombotic thrombocytopenic purpura): a cross-sectional analysis of the French national registry for thrombotic microangiopathy

Éric Mariotte, Élie Azoulay, Lionel Galicier et al. · The Lancet Haematology · 2016 · 312 citations

Medicine, Hematology, Pathology +7

Terminal Complement Inhibitor Eculizumab in Adult Patients With Atypical Hemolytic Uremic Syndrome: A Single-Arm, Open-Label Trial

Fádi Fakhouri, Maryvonne Hourmant, Josep M. Campistol et al. · American Journal of Kidney Diseases · 2016 · 308 citations · Full text

Medicine, Pharmacology, Pharmacotherapy +17