Pathogenic Variants in Complement Genes and Risk of Atypical Hemolytic Uremic Syndrome Relapse after Eculizumab Discontinuation-Reference-Cited by-同舟云学术

Pathogenic Variants in Complement Genes and Risk of Atypical Hemolytic Uremic Syndrome Relapse after Eculizumab Discontinuation

Published:2016-10-31 Issue:1 Volume:12 Page:50-59
ISSN:1555-9041
Container-title:Clinical Journal of the American Society of Nephrology
language:en
Short-container-title:CJASN

Author:

Fakhouri Fadi,Fila Marc,Provôt François,Delmas Yahsou,Barbet Christelle,Châtelet Valérie,Rafat Cédric,Cailliez Mathilde,Hogan Julien,Servais Aude,Karras Alexandre,Makdassi Raifah,Louillet Feriell,Coindre Jean-Philippe,Rondeau Eric,Loirat Chantal,Frémeaux-Bacchi Véronique

Publisher

American Society of Nephrology (ASN)

Subject

Transplantation,Nephrology,Critical Care and Intensive Care Medicine,Epidemiology

Reference25 articles.

1. Genetics and Outcome of Atypical Hemolytic Uremic Syndrome: A Nationwide French Series Comparing Children and Adults

2. Insights From the Use in Clinical Practice of Eculizumab in Adult Patients With Atypical Hemolytic Uremic Syndrome Affecting the Native Kidneys: An Analysis of 19 Cases

3. Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their Impact on Clinical Phenotype

4. Eculizumab in atypical hemolytic-uremic syndrome.;Legendre;N Engl J Med,2013

5. Efficacy and safety of eculizumab in atypical hemolytic uremic syndrome from 2-year extensions of phase 2 studies

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