Genetic analysis of the complement factor H related 5 gene in haemolytic uraemic syndrome

Giuseppe Monteferrante; Simona Brioschi; Jessica Caprioli; Gaia Pianetti; Paola Bettinaglio; Elena Bresin; Giuseppe Remuzzi; Marina Noris

doi:10.1016/j.molimm.2006.08.004

Discussion(0)

No comments yet. Be the first to comment.

Related publications

Letter2006

Complement Factor H Gene Abnormalities in Haemolytic Uraemic Syndrome: From Point Mutations to Hybrid Gene

Marina Noris, Giuseppe Remuzzi

Article2007

Complement hyperactivation may cause atypical haemolytic uraemic syndrome gain-of-function mutations in factor B

Jessica Caprioli, Giuseppe Remuzzi

Article2003

Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease

Jessica Caprioli, Federica Castelletti, Sara Bucchioni, Paola Bettinaglio, Elena Bresin, Gaia Pianetti, Sara Gamba, Simona Brioschi, Erica Daina, Giuseppe Remuzzi, Marina Noris

Article1992

Urinary excretion of platelet-activating factor in haemolytic uraemic syndrome

Ariela Benigni, Paola Boccardo, Marina Noris, Giuseppe Remuzzi, Richard L. Siegler

Article2008

Is local complement activation involved in renal damage in patients with atypical haemolytic uraemic syndrome?

Claudio Tripodo, Marina Noris, Paolo Macor, Silvia Gastoldi, Matthew C. Pickering, Marina Botto, Reinhard Würzner, Tom Eirik Mollnes, Giuseppe Remuzzi, Francesco Tedesco