Publications by authors named "Jessica Caprioli"

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Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype.
Elena Bresin, Erica Rurali, Jessica Caprioli, Pilar Sanchez-Corral, Veronique Fremeaux-Bacchi

J Am Soc Nephrol· February 2013

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Molecular basis of familial thrombotic thrombocytopenic purpura and hemolytic uremic syndrome.
Jessica Caprioli, Simona Brioschi, Giuseppe Remuzzi

Saudi J Kidney Dis Transpl· October 2012

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Thrombotic microangiopathies: from animal models to human disease and cure.
Jessica Caprioli, Giuseppe Remuzzi, Marina Noris

Contrib Nephrol· June 2011

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Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype.
Marina Noris, Jessica Caprioli, Elena Bresin, Chiara Mossali, Gaia Pianetti

Clin J Am Soc Nephrol· October 2010

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Polymorphisms of EDNRB, ATG, and ACE genes in salt-sensitive hypertension.
Jessica Caprioli, Caterina Mele, Chiara Mossali, Laura Gallizioli, Gilberta Giacchetti

Can J Physiol Pharmacol· August 2008

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A mouse model of non-Shiga toxin-associated haemolytic uraemic syndrome.
Jessica Caprioli, Giuseppe Remuzzi

Nephrol Dial Transplant· February 2008

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Mutations in FN1 cause glomerulopathy with fibronectin deposits.
Federica Castelletti, Roberta Donadelli, Federica Banterla, Friedhelm Hildebrandt, Peter F Zipfel, Jessica Caprioli

Proc Natl Acad Sci U S A· February 2008

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Complement hyperactivation may cause atypical haemolytic uraemic syndrome--gain-of-function mutations in factor B.
Jessica Caprioli, Giuseppe Remuzzi

Nephrol Dial Transplant· September 2007

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Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome.
Jessica Caprioli, Marina Noris, Simona Brioschi, Gaia Pianetti, Federica Castelletti

Blood· August 2006

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The hemolytic uremic syndromes.
Jessica Caprioli, Li Peng, Giuseppe Remuzzi

Curr Opin Crit Care· October 2005

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Complement factor H mutation in familial thrombotic thrombocytopenic purpura with ADAMTS13 deficiency and renal involvement.
Marina Noris, Sara Bucchioni, Miriam Galbusera, Roberta Donadelli, Elena Bresin, Jessica Caprioli

J Am Soc Nephrol· May 2005

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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

Hum Mol Genet· December 2003

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Familial haemolytic uraemic syndrome and an MCP mutation.
Marina Noris, Simona Brioschi, Jessica Caprioli, Marta Todeschini, Elena Bresin

Lancet· November 2003

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Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome.
Tamara Manuelian, Jens Hellwage, Seppo Meri, Jessica Caprioli, Marina Noris

J Clin Invest· April 2003

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von Willebrand factor cleaving protease (ADAMTS13) is deficient in recurrent and familial thrombotic thrombocytopenic purpura and hemolytic uremic syndrome.
Giuseppe Remuzzi, Miriam Galbusera, Marina Noris, Maria Teresa Canciani, Erica Daina, Jessica Caprioli

Blood· August 2002

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Single Strand Conformation Polymorphism (SSCP) as a quick and reliable method to genotype M235T polymorphism of angiotensinogen gene.
Paola Bettinaglio, Andrea Galbusera, Jessica Caprioli, Silvia Orisio, Annalisa Perna

Clin Biochem· July 2002

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Combined kidney and liver transplantation for familial haemolytic uraemic syndrome.
Giuseppe Remuzzi, Piero Ruggenenti, Daniela Codazzi, Marina Noris, Jessica Caprioli

Lancet· May 2002

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The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20.
Jessica Caprioli, Paola Bettinaglio, Peter F Zipfel, Barbara Amadei, Erica Daina

J Am Soc Nephrol· February 2001

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