aHUS associated with C3 gene mutation: a case with numerous relapses and favorable 20-year outcome-Reference-Cited by-同舟云学术

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aHUS associated with C3 gene mutation: a case with numerous relapses and favorable 20-year outcome

Published:2015-11-16 Issue:3 Volume:31 Page:513-517
ISSN:0931-041X
Container-title:Pediatric Nephrology
language:en
Short-container-title:Pediatr Nephrol

Author:

Siomou Ekaterini,Gkoutsias Athanasios,Serbis Anastasios,Kollios Konstantinos,Chaliasos Nikolaos,Frémeaux-Bacchi Veronique

Publisher

Springer Science and Business Media LLC

Subject

Nephrology,Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00467-015-3267-3.pdf

Reference13 articles.

1. Nester CM, Barbour T, de Cordoba SR, Dragon-Durey MA, Frémeaux-Bacchi V, Goodship TH, Kavanagh D, Noris M, Pickering M, Sanchez-Corral P, Skerka C, Zipfel P, Smith RJ (2015) Atypical aHUS: state of the art. Mol Immunol 67:31–42

2. Dragon-Durey MA, Loirat C, Cloarec S, Macher MA, Blouin J, Nivet H, Weiss L, Fridman WH, Frémeaux-Bacchi V (2005) Anti-Factor H autoantibodies associated with atypical hemolytic uremic syndrome. J Am Soc Nephrol 16:555–563

3. Sinha A, Gulati A, Saini S, Blanc C, Gupta A, Gurjar BS, Saini H, Kotresh ST, Ali U, Bhatia D, Ohri A, Kumar M, Agarwal I, Gulati S, Anand K, Vijayakumar M, Sinha R, Sethi S, Salmona M, George A, Bal V, Singh G, Dinda AK, Hari P, Rath S, Dragon-Durey MA, Bagga A, Indian HUS Registry (2014) Prompt plasma exchanges and immunosuppressive treatment improves the outcomes of anti-factor H autoantibody-associated hemolytic uremic syndrome in children. Kidney Int 85:1151–1160

4. Józsi M, Licht C, Strobel S, Zipfel SL, Richter H, Heinen S, Zipfel PF, Skerka C (2008) Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency. Blood 111:1512–1514

5. Frémeaux-Bacchi V, Miller EC, Liszewski MK, Strain L, Blouin J, Brown AL, Moghal N, Kaplan BS, Weiss RA, Lhotta K, Kapur G, Mattoo T, Nivet H, Wong W, Gie S, Hurault de Ligny B, Fischbach M, Gupta R, Hauhart R, Meunier V, Loirat C, Dragon-Durey MA, Fridman WH, Janssen BJ, Goodship TH, Atkinson JP (2008) Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome. Blood 112:4948–4952

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1. Atypical HUS with multiple complement system mutations triggered by synthetic psychoactive drug abuse: a case report;Journal of Nephrology;2023-05-05

2. The use of the drug Elizaria – a biosimilar of the original eculizumab in atypical hemolytic-uremic syndrome due to mutation of the С3 gene in children: clinical observation and literature review;Nephrology (Saint-Petersburg);2023-03-08

3. Genetic variability shapes the alternative pathway complement activity and predisposition to complement‐related diseases;Immunological Reviews;2022-09-11

4. Atypical hemolytic uremic syndrome with C3 mutation: A case report and literature review;Clinical Nephrology;2021-03-01

5. The Relevance of the MCP Risk Polymorphism to the Outcome of aHUS Associated With C3 Mutations. A Case Report;Frontiers in Immunology;2020-07-16

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