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Luciana Furci

Showing results (1-10 of 15) with videos related to

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Clinical and Experimental Nephrology|January 6, 2010
Coincident chronic inflammatory demyelinating polyneuropathy and focal segmental glomerulosclerosis: a common autoimmunity?Francesca Girolami, Giuliana Galassi, Luciana Furci, et al.
Journal of Medical Case Reports|January 12, 2010
Lipoprotein glomerulopathy treated with LDL-apheresis (Heparin-induced Extracorporeal Lipoprotein Precipitation system): a case reportGianpaolo Russi, Luciana Furci, Marco Leonelli, et al.
Journal of Nephrology|March 26, 2003
Epidermal growth factor receptor polymorphism and autosomal dominant polycystic kidney diseaseRiccardo Magistroni, Paolo Manfredini, Luciana Furci, et al.
Plos One|November 13, 2012
Identification and characterization of a new autoimmune protein in membranous nephropathy by immunoscreening of a renal cDNA libraryFabrizio Cavazzini, Riccardo Magistroni, Luciana Furci, et al.
Journal of Nephrology|September 28, 2010
Interstitial fluid obtained from kidney biopsy as new source of renal biomarkersRiccardo Magistroni, Marco Cantù, Giulia Ligabue, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 13, 2009
Proteomic analysis of urine from proteinuric patients shows a proteolitic activity directed against albuminRiccardo Magistroni, Giulia Ligabue, Valentina Lupo, et al.
Clinical Medicine Insights. Case Reports|December 19, 2013
Lipoprotein glomerulopathy associated with a mutation in apolipoprotein eRiccardo Magistroni, Marco Bertolotti, Luciana Furci, et al.
Plos One|January 17, 2018
The prevalence of autosomal dominant polycystic kidney disease (ADPKD): A meta-analysis of European literature and prevalence evaluation in the Italian province of Modena suggest that ADPKD is a rare and underdiagnosed conditionAndrea Solazzo, Francesca Testa, Silvia Giovanella, et al.
Clinical Journal of the American Society of Nephrology : CJASN|September 17, 2020
Evaluation of the Classification Accuracy of the Kidney Biopsy Direct Immunofluorescence through Convolutional Neural NetworksGiulia Ligabue, Federico Pollastri, Francesco Fontana, et al.
Kidney International|June 6, 2003
Precocious activation of genes of the renin-angiotensin system and the fibrogenic cascade in IgA glomerulonephritisDorella Del Prete, Giovanni Gambaro, Antonio Lupo, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Clinical and Experimental Nephrology|January 6, 2010
Coincident chronic inflammatory demyelinating polyneuropathy and focal segmental glomerulosclerosis: a common autoimmunity?Francesca Girolami, Giuliana Galassi, Luciana Furci, et al.
Journal of Medical Case Reports|January 12, 2010
Lipoprotein glomerulopathy treated with LDL-apheresis (Heparin-induced Extracorporeal Lipoprotein Precipitation system): a case reportGianpaolo Russi, Luciana Furci, Marco Leonelli, et al.
Journal of Nephrology|March 26, 2003
Epidermal growth factor receptor polymorphism and autosomal dominant polycystic kidney diseaseRiccardo Magistroni, Paolo Manfredini, Luciana Furci, et al.
Plos One|November 13, 2012
Identification and characterization of a new autoimmune protein in membranous nephropathy by immunoscreening of a renal cDNA libraryFabrizio Cavazzini, Riccardo Magistroni, Luciana Furci, et al.
Journal of Nephrology|September 28, 2010
Interstitial fluid obtained from kidney biopsy as new source of renal biomarkersRiccardo Magistroni, Marco Cantù, Giulia Ligabue, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 13, 2009
Proteomic analysis of urine from proteinuric patients shows a proteolitic activity directed against albuminRiccardo Magistroni, Giulia Ligabue, Valentina Lupo, et al.
Clinical Medicine Insights. Case Reports|December 19, 2013
Lipoprotein glomerulopathy associated with a mutation in apolipoprotein eRiccardo Magistroni, Marco Bertolotti, Luciana Furci, et al.
Plos One|January 17, 2018
The prevalence of autosomal dominant polycystic kidney disease (ADPKD): A meta-analysis of European literature and prevalence evaluation in the Italian province of Modena suggest that ADPKD is a rare and underdiagnosed conditionAndrea Solazzo, Francesca Testa, Silvia Giovanella, et al.
Clinical Journal of the American Society of Nephrology : CJASN|September 17, 2020
Evaluation of the Classification Accuracy of the Kidney Biopsy Direct Immunofluorescence through Convolutional Neural NetworksGiulia Ligabue, Federico Pollastri, Francesco Fontana, et al.
Kidney International|June 6, 2003
Precocious activation of genes of the renin-angiotensin system and the fibrogenic cascade in IgA glomerulonephritisDorella Del Prete, Giovanni Gambaro, Antonio Lupo, et al.
Pageof 2