Stephanie Ngo
Paris, France
Last Updated: 09/26/2026
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Found 14 publications
Complement activation drives a compartmentalized innate immune response in C3 glomerulopathy contributing to the disease phenotype.
Journal: Kidney international
Published: January 19, 2025
Pseudohyperkalemia and thrombocytosis
Journal: La Revue de medecine interne
Published: September 26, 2020
Abdominal pain and vomiting in a 66-year-old man
Journal: La Revue de medecine interne
Published: October 24, 2016
Agranulocytosis related to fluindione: A case report
Journal: La Revue de medecine interne
Published: November 13, 2014
Which place for direct oral anticoagulants in routine hospital medical practice?
Journal: La Revue de medecine interne
Published: October 07, 2014
Complement deficiencies and human diseases
Journal: Annales de biologie clinique
Published: May 31, 2014
Complement factor B mutations in atypical hemolytic uremic syndrome-disease-relevant or benign?
Journal: Journal of the American Society of Nephrology : JASN
Published: March 22, 2014
Facial diplegia as the presenting feature of Lyme disease
Journal: La Revue de medecine interne
Published: December 21, 2013
Anti-factor H autoantibodies assay.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: November 13, 2013
Functional evaluation of factor H genetic and acquired abnormalities: application for atypical hemolytic uremic syndrome (aHUS).
Journal: Methods in molecular biology (Clifton, N.J.)
Published: November 13, 2013
C3 nephritic factor associated with C3 glomerulopathy in children.
Journal: Pediatric nephrology (Berlin, Germany)
Published: May 01, 2013
Last Updated: 09/26/2026