Plasma therapy in atypical haemolytic uremic syndrome: lessons from a family with a factor H mutation

Author:

Davin Jean Claude,Strain Lisa,Goodship Tim H. J.

Publisher

Springer Science and Business Media LLC

Subject

Nephrology,Pediatrics, Perinatology and Child Health

Reference21 articles.

1. Kavanagh D, Goodship TH, Richards A (2006) Atypical haemolytic uraemic syndrome. Br Med Bull 77:1–18

2. Caprioli J, Noris M, Brioschi S, Pianetti G, Castelletti F, Bettinaglio P, Mele C, Bresin E, Cassis L, Gamba S, Porrati F, Bucchioni S, Monteferrante G, Fang CJ, Liszewski MK, Kavanagh D, Atkinson JP, Remuzzi G (2006) Genetics of HUS: the impact of MCP, CFH and IF mutations on clinical presentation, response to treatment, and outcome. Blood 108:1267–1279

3. Sellier-Leclerc AL, Fremeaux-Bacchi V, Dragon-Durey MA, Macher MA, Niaudet P, Guest G, Boudaillez B, Bouissou F, Deschesnes G, Gie S, Tsimaratos M, Fischbach M, Morin D, Nivet H, Alberti C, Loirat C, French Society of Pediatric Nephrology (2007) Differential impact of complement mutations on clinical characteristics in atypical HUS. J Am Soc Nephrol 18:2392–2400

4. Saunders RE, Abarrategui-Garrido C, Frémeaux-Bacchi V, Goicoechea de Jorge E, Goodship THJ, Lopez Trascasa M, Noris M, Ponce Castro IM, Remuzzi G, Rodriguez de Cordoba S, Sanchez-Corral P, Skerka C, Zipfel PF, Perkins SJ (2007) The interactive Factor H-atypical hemolytic uremic syndrome mutation database and Website: Update and integration of membrane cofactor protein and factor I mutations with structural models. Hum Mutat 28:222–234

5. Geelen J, van den Dries K, Roos A, van de Kar N, de Kat Angelino K, Klasen I, Monnens L, van den Heuvel L (2007) A missense mutation in factor I (IF) predisposes to atypical haemolytic uraemic syndrome. Pediatr Nephrol 22:371–375

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