Successful treatment of neonatal atypical hemolytic uremic syndrome with C5 monoclonal antibody

This publication has 19 references indexed in Scilit:

• Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome
  Clinical Journal of the American Society of Nephrology, 2015
• An international consensus approach to the management of atypical hemolytic uremic syndrome in children
  Pediatric Nephrology, 2015
• Complement Mutations in Diacylglycerol Kinase-ε–Associated Atypical Hemolytic Uremic Syndrome
  Clinical Journal of the American Society of Nephrology, 2014
• An audit analysis of a guideline for the investigation and initial therapy of diarrhea negative (atypical) hemolytic uremic syndrome
  Pediatric Nephrology, 2014
• Genetics and Outcome of Atypical Hemolytic Uremic Syndrome
  Clinical Journal of the American Society of Nephrology, 2013
• Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome
  Nature Genetics, 2013
• Combined Complement Gene Mutations in Atypical Hemolytic Uremic Syndrome Influence Clinical Phenotype
  Journal of the American Society of Nephrology, 2013
• Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies
  Nature Reviews Nephrology, 2012
• Syndrome hémolytique et urémique avec atteinte neurologique sévère : quelle prise en charge ?
  Archives de Pédiatrie, 2012
• Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their Impact on Clinical Phenotype
  Clinical Journal of the American Society of Nephrology, 2010