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Luisa Murer

Showing results (61-70 of 93) with videos related to

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Human Mutation|October 21, 2010
Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tractStefania Gimelli, Gianluca Caridi, Silvana Beri, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 16, 2016
Renal transplantation in sensitized children and young adults: a nationwide approachLuca Dello Strologo, Luisa Murer, Isabella Guzzo, et al.
Clinical Transplantation|February 5, 2009
Longitudinal evaluation of mycophenolic acid pharmacokinetics in pediatric kidney transplant recipients. The role of post-transplant clinical and therapeutic variablesLuciana Ghio, Mariano Ferraresso, Graziella Zacchello, et al.
International Journal of Molecular Sciences|January 18, 2020
Genetic Analyses in Dent Disease and Characterization of CLCN5 Mutations in Kidney BiopsiesLisa Gianesello, Monica Ceol, Loris Bertoldi, et al.
Journal of the American Society of Nephrology : JASN|July 26, 2014
Heterogeneous genetic alterations in sporadic nephrotic syndrome associate with resistance to immunosuppressionSabrina Giglio, Aldesia Provenzano, Benedetta Mazzinghi, 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.
Journal of the American Society of Nephrology : JASN|September 15, 2007
COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvementFrancesca Diomedi-Camassei, Silvia Di Giandomenico, Filippo M Santorelli, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 16, 2013
Encapsulating peritoneal sclerosis in paediatric peritoneal dialysis patients: the experience of the Italian Registry of Pediatric Chronic DialysisEnrico Vidal, Alberto Edefonti, Flora Puteo, et al.
Journal of the American Society of Nephrology : JASN|October 15, 2017
Cluster Analysis Identifies Distinct Pathogenetic Patterns in C3 Glomerulopathies/Immune Complex-Mediated Membranoproliferative GNParaskevas Iatropoulos, Erica Daina, Manuela Curreri, et al.
Molecular Immunology|February 20, 2016
Complement gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcomeParaskevas Iatropoulos, Marina Noris, Caterina Mele, et al.
Pageof 10

Showing results (61-70 of 93) with videos related to

Sort By:
Pageof 10
Human Mutation|October 21, 2010
Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tractStefania Gimelli, Gianluca Caridi, Silvana Beri, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 16, 2016
Renal transplantation in sensitized children and young adults: a nationwide approachLuca Dello Strologo, Luisa Murer, Isabella Guzzo, et al.
Clinical Transplantation|February 5, 2009
Longitudinal evaluation of mycophenolic acid pharmacokinetics in pediatric kidney transplant recipients. The role of post-transplant clinical and therapeutic variablesLuciana Ghio, Mariano Ferraresso, Graziella Zacchello, et al.
International Journal of Molecular Sciences|January 18, 2020
Genetic Analyses in Dent Disease and Characterization of CLCN5 Mutations in Kidney BiopsiesLisa Gianesello, Monica Ceol, Loris Bertoldi, et al.
Journal of the American Society of Nephrology : JASN|July 26, 2014
Heterogeneous genetic alterations in sporadic nephrotic syndrome associate with resistance to immunosuppressionSabrina Giglio, Aldesia Provenzano, Benedetta Mazzinghi, 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.
Journal of the American Society of Nephrology : JASN|September 15, 2007
COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvementFrancesca Diomedi-Camassei, Silvia Di Giandomenico, Filippo M Santorelli, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 16, 2013
Encapsulating peritoneal sclerosis in paediatric peritoneal dialysis patients: the experience of the Italian Registry of Pediatric Chronic DialysisEnrico Vidal, Alberto Edefonti, Flora Puteo, et al.
Journal of the American Society of Nephrology : JASN|October 15, 2017
Cluster Analysis Identifies Distinct Pathogenetic Patterns in C3 Glomerulopathies/Immune Complex-Mediated Membranoproliferative GNParaskevas Iatropoulos, Erica Daina, Manuela Curreri, et al.
Molecular Immunology|February 20, 2016
Complement gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcomeParaskevas Iatropoulos, Marina Noris, Caterina Mele, et al.
Pageof 10