Amanote Research

Amanote Research

    RegisterSign In

Discover open access scientific publications

Search, annotate, share and cite publications


Publications by François Provot

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

Journal of the American Society of Nephrology : JASN
MedicineNephrology
2010English

Related publications

Complement Factor H Gene Mutation Associated With Autosomal Recessive Atypical Hemolytic Uremic Syndrome

American Journal of Human Genetics
Genetics
1999English

Acute Systolic Heart Failure Associated With Complement-Mediated Hemolytic Uremic Syndrome

Case Reports in Hematology
2015English

The Development of Atypical Hemolytic Uremic Syndrome Depends on Complement C5

Journal of the American Society of Nephrology : JASN
MedicineNephrology
2010English

Comprehensive Genetic Analysis of Complement and Coagulation Genes in Atypical Hemolytic Uremic Syndrome

Journal of the American Society of Nephrology : JASN
MedicineNephrology
2013English

D+ Hemolytic Uremic Syndrome

Paediatrica Indonesiana
2016English

Atypical Hemolytic-Uremic Syndrome

2020English

Complement Biomarkers of Hemolytic Uremic Syndrome—If Not One Thing, Maybe Another

Mayo Clinic Proceedings
Medicine
2018English

Electrolyte Excretion in the Hemolytic Uremic Syndrome.

Nihon Shoni Jinzobyo Gakkai Zasshi
1996English

Cell Adhesion Molecules in Childrenwith Diarrhea-Associated Hemolytic Uremic Syndrome

2018English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy