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Records 1-10

Query Trace: Thrombocytopenia and CD46[orginal query]

Complement genes strongly predict recurrence and graft outcome in adult renal transplant recipients with atypical hemolytic and uremic syndrome. American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons 2013 Mar 13 (3): 663-75. Le Quintrec M, Zuber J, Moulin B, Kamar N, Jablonski M, Lionet A, Chatelet V, Mousson C, Mourad G, Bridoux F, Cassuto E, Loirat C, Rondeau E, Delahousse M, Frémeaux-Bacchi Similar articles in PubMed
Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype. Journal of the American Society of Nephrology : JASN 2013 Feb 24 (3): 475-86. Bresin Elena, Rurali Erica, Caprioli Jessica, Sanchez-Corral Pilar, Fremeaux-Bacchi Veronique, Rodriguez de Cordoba Santiago, Pinto Sheila, Goodship Timothy H J, Alberti Marta, Ribes David, Valoti Elisabetta, Remuzzi Giuseppe, Noris Marina, Similar articles in PubMed
Common genetic variants in complement genes other than CFH, CD46 and the CFHRs are not associated with aHUS. Molecular immunology 2012 Jan 49 (4): 640-8. Ermini Luca, Goodship Timothy H J, Strain Lisa, Weale Michael E, Sacks Steven H, Cordell Heather J, Fremeaux-Bacchi Veronique, Sheerin Neil Similar articles in PubMed
Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype. Clinical journal of the American Society of Nephrology : CJASN 2010 Oct 5 (10): 1844-59. Noris Marina, Caprioli Jessica, Bresin Elena, Mossali Chiara, Pianetti Gaia, Gamba Sara, Daina Erica, Fenili Chiara, Castelletti Federica, Sorosina Annalisa, Piras Rossella, Donadelli Roberta, Maranta Ramona, van der Meer Irene, Conway Edward M, Zipfel Peter F, Goodship Timothy H, Remuzzi Giusep Similar articles in PubMed
Genetic disorders in complement (regulating) genes in patients with atypical haemolytic uraemic syndrome (aHUS). Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2010 Jul 25 (7): 2195-202. Westra Dineke, Volokhina Elena, van der Heijden Eefje, Vos Annemieke, Huigen Marleen, Jansen Jitske, van Kaauwen Edwin, van der Velden Thea, van de Kar Nicole, van den Heuvel Lambe Similar articles in PubMed
Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome. Human mutation 2010 Jun 31 (6): E1445-60. Maga Tara K, Nishimura Carla J, Weaver Amy E, Frees Kathy L, Smith Richard J Similar articles in PubMed
Epidemiological approach to identifying genetic predispositions for atypical hemolytic uremic syndrome. Annals of human genetics 2010 Jan 74 (1): 17-26. Sullivan Maren, Erlic Zoran, Hoffmann Michael M, Arbeiter Klaus, Patzer Ludwig, Budde Klemens, Hoppe Bernd, Zeier Martin, Lhotta Karl, Rybicki Lisa A, Bock Andreas, Berisha Gani, Neumann Hartmut P Similar articles in PubMed
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. Journal of immunology (Baltimore, Md. : 1950) 2008 May 180 (9): 6385-91. Blom Anna M, Bergström Frida, Edey Matthew, Diaz-Torres Martha, Kavanagh David, Lampe Anne, Goodship Judith A, Strain Lisa, Moghal Nadeem, McHugh Mary, Inward Carol, Tomson Charles, Frémeaux-Bacchi Véronique, Villoutreix Bruno O, Goodship Timothy H Similar articles in PubMed
Genetic analysis of the complement factor H related 5 gene in haemolytic uraemic syndrome. Molecular immunology 2007 Mar 44 (7): 1704-8. Monteferrante G, Brioschi S, Caprioli J, Pianetti G, Bettinaglio P, Bresin E, Remuzzi G, Noris Similar articles in PubMed
Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome. Blood 2006 Aug 108 (4): 1267-79. Caprioli Jessica, Noris Marina, Brioschi Simona, Pianetti Gaia, Castelletti Federica, Bettinaglio Paola, Mele Caterina, Bresin Elena, Cassis Linda, Gamba Sara, Porrati Francesca, Bucchioni Sara, Monteferrante Giuseppe, Fang Celia J, Liszewski M K, Kavanagh David, Atkinson John P, Remuzzi Giuseppe, Similar articles in PubMed

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