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Gianfranco Rizzoni

Showing results (21-30 of 32) with videos related to

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Journal of Nephrology|June 10, 2005
One-year angiotensin-converting enzyme inhibition plus mycophenolate mofetil immunosuppression in the course of early IgA nephropathy: a multicenter, randomised, controlled studyAntonio Dal Canton, Amore Amore, Giancarlo Barbano, et al.
Emerging Infectious Diseases|January 21, 2003
Shiga toxin-producing Escherichia coli infections associated with hemolytic uremic syndrome, Italy, 1988-2000Alberto E Tozzi, Alfredo Caprioli, Fabio Minelli, et al.
Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis|October 20, 2004
Chronic peritoneal dialysis catheters in children: a fifteen-year experience of the Italian Registry of Pediatric Chronic Peritoneal DialysisStefano Rinaldi, Francesco Sera, Enrico Verrina, et al.
Seminars in Thrombosis and Hemostasis|April 1, 2006
Epidemiology, clinical presentation, and pathophysiology of atypical and recurrent hemolytic uremic syndromeL Bernd Zimmerhackl, Nesir Besbas, Therese Jungraithmayr, et al.
Journal of Clinical Microbiology|February 4, 2006
Shiga toxins present in the gut and in the polymorphonuclear leukocytes circulating in the blood of children with hemolytic-uremic syndromeMaurizio Brigotti, Alfredo Caprioli, Alberto E Tozzi, et al.
Journal of the American Society of Nephrology : JASN|April 23, 2003
Broadening the spectrum of diseases related to podocin mutationsGianluca Caridi, Roberta Bertelli, Marco Di Duca, et al.
Pediatric Nephrology (Berlin, Germany)|February 13, 2003
Confirmation of the ATP6B1 gene as responsible for distal renal tubular acidosisRainer Ruf, Cornelia Rensing, Rezan Topaloglu, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|May 31, 2003
Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocinRoberta Bertelli, Fabrizio Ginevri, Gianluca Caridi, et al.
Journal of the American Society of Nephrology : JASN|September 20, 2002
Comparison between SLC3A1 and SLC7A9 cystinuria patients and carriers: a need for a new classificationLuca Dello Strologo, Elon Pras, Claudia Pontesilli, et al.
Journal of the American Society of Nephrology : JASN|September 30, 2003
X-linked Alport syndrome: natural history and genotype-phenotype correlations in girls and women belonging to 195 families: a "European Community Alport Syndrome Concerted Action" studyJean Philippe Jais, Bertrand Knebelmann, Iannis Giatras, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Journal of Nephrology|June 10, 2005
One-year angiotensin-converting enzyme inhibition plus mycophenolate mofetil immunosuppression in the course of early IgA nephropathy: a multicenter, randomised, controlled studyAntonio Dal Canton, Amore Amore, Giancarlo Barbano, et al.
Emerging Infectious Diseases|January 21, 2003
Shiga toxin-producing Escherichia coli infections associated with hemolytic uremic syndrome, Italy, 1988-2000Alberto E Tozzi, Alfredo Caprioli, Fabio Minelli, et al.
Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis|October 20, 2004
Chronic peritoneal dialysis catheters in children: a fifteen-year experience of the Italian Registry of Pediatric Chronic Peritoneal DialysisStefano Rinaldi, Francesco Sera, Enrico Verrina, et al.
Seminars in Thrombosis and Hemostasis|April 1, 2006
Epidemiology, clinical presentation, and pathophysiology of atypical and recurrent hemolytic uremic syndromeL Bernd Zimmerhackl, Nesir Besbas, Therese Jungraithmayr, et al.
Journal of Clinical Microbiology|February 4, 2006
Shiga toxins present in the gut and in the polymorphonuclear leukocytes circulating in the blood of children with hemolytic-uremic syndromeMaurizio Brigotti, Alfredo Caprioli, Alberto E Tozzi, et al.
Journal of the American Society of Nephrology : JASN|April 23, 2003
Broadening the spectrum of diseases related to podocin mutationsGianluca Caridi, Roberta Bertelli, Marco Di Duca, et al.
Pediatric Nephrology (Berlin, Germany)|February 13, 2003
Confirmation of the ATP6B1 gene as responsible for distal renal tubular acidosisRainer Ruf, Cornelia Rensing, Rezan Topaloglu, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|May 31, 2003
Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocinRoberta Bertelli, Fabrizio Ginevri, Gianluca Caridi, et al.
Journal of the American Society of Nephrology : JASN|September 20, 2002
Comparison between SLC3A1 and SLC7A9 cystinuria patients and carriers: a need for a new classificationLuca Dello Strologo, Elon Pras, Claudia Pontesilli, et al.
Journal of the American Society of Nephrology : JASN|September 30, 2003
X-linked Alport syndrome: natural history and genotype-phenotype correlations in girls and women belonging to 195 families: a "European Community Alport Syndrome Concerted Action" studyJean Philippe Jais, Bertrand Knebelmann, Iannis Giatras, et al.
Pageof 4