Aude Servais
Hôpital Necker-Enfants Malades(FR)
Publications by Year
Research Areas
Renal Diseases and Glomerulopathies, Complement system in diseases, Metabolism and Genetic Disorders, Biomedical Research and Pathophysiology, Amino Acid Enzymes and Metabolism
Most-Cited Works
- → Genetics and Outcome of Atypical Hemolytic Uremic Syndrome(2013)703 cited
- → C3 glomerulopathy: consensus report(2013)627 cited
- → Suggested guidelines for the diagnosis and management of urea cycle disorders(2012)619 cited
- → Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies(2012)558 cited
- → Suggested guidelines for the diagnosis and management of urea cycle disorders: First revision(2019)449 cited
- → Year of Diagnosis, Features at Presentation, and Risk of Recurrence in Patients with Pheochromocytoma or Secreting Paraganglioma(2005)379 cited
- → Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome(2006)288 cited
- → Cysteamine therapy delays the progression of nephropathic cystinosis in late adolescents and adults(2011)237 cited
- → Preemptive rituximab infusions after remission efficiently prevent relapses in acquired thrombotic thrombocytopenic purpura(2014)183 cited
- → Pathogenic Variants in Complement Genes and Risk of Atypical Hemolytic Uremic Syndrome Relapse after Eculizumab Discontinuation(2016)179 cited