Complement Factor H–Related Protein 1 Deficiency and Factor H Antibodies in Pediatric Patients with Atypical Hemolytic Uremic Syndrome-Reference-Cited by-同舟云学术

Complement Factor H–Related Protein 1 Deficiency and Factor H Antibodies in Pediatric Patients with Atypical Hemolytic Uremic Syndrome

Published:2012-12-14 Issue:3 Volume:8 Page:407-415
ISSN:1555-9041
Container-title:Clinical Journal of the American Society of Nephrology
language:en
Short-container-title:CJASN

Author:

Hofer Johannes,Janecke Andreas R.,Zimmerhackl L.B.,Riedl Magdalena,Rosales Alejandra,Giner Thomas,Cortina Gerard,Haindl Carola J.,Petzelberger Barbara,Pawlik Miriam,Jeller Verena,Vester Udo,Gadner Bettina,van Husen Michael,Moritz Michael L.,Würzner Reinhard,Jungraithmayr Therese,

Publisher

American Society of Nephrology (ASN)

Subject

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

Reference43 articles.

1. Need for Long-term Follow-up in Enterohemorrhagic Escherichia coli–Associated Hemolytic Uremic Syndrome Due to Late-Emerging Sequelae

2. Mycophenolate mofetil promotes prolonged improvement of renal dysfunction after pediatric liver transplantation: Experience of a single center

3. A classification of hemolytic uremic syndrome and thrombotic thrombocytopenic purpura and related disorders.;Besbas;Kidney Int,2006

4. Differential Impact of Complement Mutations on Clinical Characteristics in Atypical Hemolytic Uremic Syndrome

5. Renal transplantation in HUS patients with disorders of complement regulation

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