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Jessica Caprioli

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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 19, 2007
Complement hyperactivation may cause atypical haemolytic uraemic syndrome--gain-of-function mutations in factor BJessica Caprioli, Giuseppe Remuzzi
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 25, 2007
A mouse model of non-Shiga toxin-associated haemolytic uraemic syndromeJessica Caprioli, Giuseppe Remuzzi
Current Opinion in Critical Care|September 22, 2005
The hemolytic uremic syndromesJessica Caprioli, Li Peng, Giuseppe Remuzzi
Saudi Journal of Kidney Diseases and Transplantation : an Official Publication of the Saudi Center for Organ Transplantation, Saudi Arabia|July 28, 2007
Molecular basis of familial thrombotic thrombocytopenic purpura and hemolytic uremic syndromeJessica Caprioli, Simona Brioschi, Giuseppe Remuzzi
Contributions to Nephrology|January 22, 2011
Thrombotic microangiopathies: from animal models to human disease and cureJessica Caprioli, Giuseppe Remuzzi, Marina Noris
Lancet (London, England)|May 22, 2002
Combined kidney and liver transplantation for familial haemolytic uraemic syndromeGiuseppe Remuzzi, Piero Ruggenenti, Daniela Codazzi, et al.
Canadian Journal of Physiology and Pharmacology|September 2, 2008
Polymorphisms of EDNRB, ATG, and ACE genes in salt-sensitive hypertensionJessica Caprioli, Caterina Mele, Chiara Mossali, et al.
Lancet (London, England)|November 15, 2003
Familial haemolytic uraemic syndrome and an MCP mutationMarina Noris, Simona Brioschi, Jessica Caprioli, et al.
Clinical Biochemistry|September 25, 2002
Single Strand Conformation Polymorphism (SSCP) as a quick and reliable method to genotype M235T polymorphism of angiotensinogen genePaola Bettinaglio, Andrea Galbusera, Jessica Caprioli, et al.
Journal of the American Society of Nephrology : JASN|April 1, 2005
Complement factor H mutation in familial thrombotic thrombocytopenic purpura with ADAMTS13 deficiency and renal involvementMarina Noris, Sara Bucchioni, Miriam Galbusera, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 19, 2007
Complement hyperactivation may cause atypical haemolytic uraemic syndrome--gain-of-function mutations in factor BJessica Caprioli, Giuseppe Remuzzi
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 25, 2007
A mouse model of non-Shiga toxin-associated haemolytic uraemic syndromeJessica Caprioli, Giuseppe Remuzzi
Current Opinion in Critical Care|September 22, 2005
The hemolytic uremic syndromesJessica Caprioli, Li Peng, Giuseppe Remuzzi
Saudi Journal of Kidney Diseases and Transplantation : an Official Publication of the Saudi Center for Organ Transplantation, Saudi Arabia|July 28, 2007
Molecular basis of familial thrombotic thrombocytopenic purpura and hemolytic uremic syndromeJessica Caprioli, Simona Brioschi, Giuseppe Remuzzi
Contributions to Nephrology|January 22, 2011
Thrombotic microangiopathies: from animal models to human disease and cureJessica Caprioli, Giuseppe Remuzzi, Marina Noris
Lancet (London, England)|May 22, 2002
Combined kidney and liver transplantation for familial haemolytic uraemic syndromeGiuseppe Remuzzi, Piero Ruggenenti, Daniela Codazzi, et al.
Canadian Journal of Physiology and Pharmacology|September 2, 2008
Polymorphisms of EDNRB, ATG, and ACE genes in salt-sensitive hypertensionJessica Caprioli, Caterina Mele, Chiara Mossali, et al.
Lancet (London, England)|November 15, 2003
Familial haemolytic uraemic syndrome and an MCP mutationMarina Noris, Simona Brioschi, Jessica Caprioli, et al.
Clinical Biochemistry|September 25, 2002
Single Strand Conformation Polymorphism (SSCP) as a quick and reliable method to genotype M235T polymorphism of angiotensinogen genePaola Bettinaglio, Andrea Galbusera, Jessica Caprioli, et al.
Journal of the American Society of Nephrology : JASN|April 1, 2005
Complement factor H mutation in familial thrombotic thrombocytopenic purpura with ADAMTS13 deficiency and renal involvementMarina Noris, Sara Bucchioni, Miriam Galbusera, et al.
Pageof 2