Article Information
PubMed
Published By
Print ISSN
Online ISSN
History
- Received for publication August 1, 2006
- Accepted for publication April 12, 2007
- Published online July 26, 2007.
Article Versions
- Earlier version (June 28, 2007 - 05:25).
- You are viewing the most recent version of this article.
Copyright & Usage
© 2007 American Society of Nephrology
Author Information
- Anne-Laure Sellier-Leclerc*,
- Veronique Fremeaux-Bacchi†,
- Marie-Agnès Dragon-Durey†,
- Marie-Alice Macher*,
- Patrick Niaudet‡,
- Geneviève Guest‡,
- Bernard Boudailliez§,
- François Bouissou‖,
- Georges Deschenes¶,
- Sophie Gie**,
- Michel Tsimaratos††,
- Michel Fischbach‡‡,
- Denis Morin§§,
- Hubert Nivet‖∥,
- Corinne Alberti¶¶,
- Chantal Loirat* and
- for the French Society of Pediatric Nephrology
- *Assistance Publique–Hôpitaux de Paris, Service de Néphrologie Pédiatrique, Hôpital Robert Debré, Université Paris VII, Faculté de Médecine Denis Diderot, Paris; †Assistance Publique–Hôpitaux de Paris, Laboratoire d'Immunologie Biologique, Hôpital Européen Georges Pompidou, Paris; ‡Assistance Publique–Hôpitaux de Paris, Service de Néphrologie Pédiatrique, Hôpital Necker-Enfants Malades, Paris; §Département de Pédiatrie, Hôpital Nord, Amiens; ‖Service de Néphrologie Pédiatrique, Hôpital des Enfants, Toulouse; ¶Assistance Publique–Hôpitaux de Paris, Service de Néphrologie Pédiatrique, Hôpital Trousseau, Paris; **Service de Néphrologie, Hôpital de Pontchaillou, Rennes; ††Service de Néphrologie, Hôpital de la Timone, Marseille; ‡‡Service de Pédiatrie, Hôpital Hautepierre, Strasbourg; §§Service de Pédiatrie 1, Hôpital Arnault de Villeneuve, Montpellier; ‖∥Service de Néphrologie, Hôpital de Clocheville, Tours; and ¶¶Assistance Publique–Hôpitaux de Paris, Hôpital Robert Debré, Unité d'Epidémiologie Clinique, Paris, France
- Correspondence:
Dr. Chantal Loirat, Service de Néphrologie, Assistance Publique-Hôpitaux de Paris, Hôpital Robert Debré, 48 Boulevard Sérurier, 75 019 Paris, France. Phone: +33-1-4003-2146; Fax: +33-1-4003-2468; chantal.loirat{at}rdb.aphp.fr
Statistics from Altmetric.com
Article usage
Cited By...
In this issue
Differential Impact of Complement Mutations on Clinical Characteristics in Atypical Hemolytic Uremic Syndrome
Jump to section
More in this TOC Section
Cited By...
- Complement Gene Variants and Shiga Toxin-Producing Escherichia coli-Associated Hemolytic Uremic Syndrome: Retrospective Genetic and Clinical Study
- Brain microvascular endothelial cells exhibit lower activation of the alternative complement pathway than glomerular microvascular endothelial cells
- Maternal and Fetal Outcomes of Pregnancies in Women with Atypical Hemolytic Uremic Syndrome
- Hemolytic Uremic Syndrome in Pregnancy and Postpartum
- Eculizumab in a child with atypical haemolytic uraemic syndrome and haemophagocytic lymphohistiocytosis triggered by cytomegalovirus infection
- Atypical hemolytic uremic syndrome
- High-Throughput Genetic Testing for Thrombotic Microangiopathies and C3 Glomerulopathies
- The long-term outcomes of atypical haemolytic uraemic syndrome: a national surveillance study
- What's new in the diagnosis and pathophysiology of thrombotic thrombocytopenic purpura
- Kidney Disease Caused by Dysregulation of the Complement Alternative Pathway: An Etiologic Approach
- Eculizumab in Anti-Factor H Antibodies Associated With Atypical Hemolytic Uremic Syndrome
- Genetics and Outcome of Atypical Hemolytic Uremic Syndrome: A Nationwide French Series Comparing Children and Adults
- Complement Factor H-Related Protein 1 Deficiency and Factor H Antibodies in Pediatric Patients with Atypical Hemolytic Uremic Syndrome
- Combined Complement Gene Mutations in Atypical Hemolytic Uremic Syndrome Influence Clinical Phenotype
- Atypical hemolytic uremic syndrome: what is it, how is it diagnosed, and how is it treated?
- Factor I Autoantibodies in Patients with Atypical Hemolytic Uremic Syndrome: Disease-Associated or an Epiphenomenon?
- Too Much of a Good Thing at the Site of Tissue Injury: The Instructive Example of the Complement System Predisposing to Thrombotic Microangiopathy
- Clinical Features of Anti-Factor H Autoantibody-Associated Hemolytic Uremic Syndrome
- Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their Impact on Clinical Phenotype
- Pregnancy-Associated Hemolytic Uremic Syndrome Revisited in the Era of Complement Gene Mutations
- Pulling the Trigger in Atypical Hemolytic Uremic Syndrome: The Role of Pregnancy
- Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome
- Complement Inhibitor Eculizumab in Atypical Hemolytic Uremic Syndrome
- A Large Family with a Gain-of-Function Mutation of Complement C3 Predisposing to Atypical Hemolytic Uremic Syndrome, Microhematuria, Hypertension and Chronic Renal Failure
- The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome
- Liver-Kidney Transplantation to Cure Atypical Hemolytic Uremic Syndrome
- Factor H, membrane cofactor protein, and factor I mutations in patients with hemolysis, elevated liver enzymes, and low platelet count syndrome
- A Novel Non-Synonymous Polymorphism (p.Arg240His) in C4b-Binding Protein Is Associated with Atypical Hemolytic Uremic Syndrome and Leads to Impaired Alternative Pathway Cofactor Activity