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Claudia Izzi

Showing results (41-50 of 80) with videos related to

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Kidney International|January 8, 2015
Tubulointerstitial nephritis is a dominant feature of hereditary apolipoprotein A-I amyloidosisGina Gregorini, Claudia Izzi, Pietro Ravani, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|April 25, 2006
IgA nephropathy: the presence of familial disease does not confer an increased risk for progressionClaudia Izzi, Pietro Ravani, Diletta Torres, et al.
Journal of the American Society of Nephrology : JASN|April 15, 2005
Familial vesicoureteral reflux: testing replication of linkage in seven new multigenerational kindredsSimone Sanna-Cherchi, Adam Reese, Terry Hensle, et al.
Clinical Kidney Journal|December 11, 2025
Tolvaptan in Autosomal Dominant Polycystic Kidney Disease (ADPKD): a multicenter real life Italian experienceLaura Econimo, Diego Toso, Giovambattista Capasso, et al.
Genetics Research|March 5, 2019
Discrepant molecular and clinical diagnoses in Beckwith-Wiedemann and Silver-Russell syndromesDeborah J G Mackay, Jet Bliek, Maria Paola Lombardi, et al.
European Journal of Medical Genetics|June 25, 2013
Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterationsChiara Migliore, Emmanouil Athanasakis, Sophie Dahoun, et al.
Kidney International|June 19, 2009
Renal outcome in patients with congenital anomalies of the kidney and urinary tractSimone Sanna-Cherchi, Pietro Ravani, Valentina Corbani, et al.
Kidney International|January 13, 2012
Urinary secretion and extracellular aggregation of mutant uromodulin isoformsCéline Schaeffer, Angela Cattaneo, Matteo Trudu, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|April 28, 2012
[Mutant uromodulin is secreted in the urine of patients with familial hyperuricemic nephropathy and induces the formation of extracellular aggregates]Céline Schaeffer, Angela Cattaneo, Matteo Trudu, et al.
Italian Journal of Pediatrics|November 17, 2018
A new case report of severe mucopolysaccharidosis type VII: diagnosis, treatment with haematopoietic cell transplantation and prenatal diagnosis in a second pregnancyFrancesca Furlan, Attilio Rovelli, Miriam Rigoldi, et al.
Pageof 8

Showing results (41-50 of 80) with videos related to

Sort By:
Pageof 8
Kidney International|January 8, 2015
Tubulointerstitial nephritis is a dominant feature of hereditary apolipoprotein A-I amyloidosisGina Gregorini, Claudia Izzi, Pietro Ravani, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|April 25, 2006
IgA nephropathy: the presence of familial disease does not confer an increased risk for progressionClaudia Izzi, Pietro Ravani, Diletta Torres, et al.
Journal of the American Society of Nephrology : JASN|April 15, 2005
Familial vesicoureteral reflux: testing replication of linkage in seven new multigenerational kindredsSimone Sanna-Cherchi, Adam Reese, Terry Hensle, et al.
Clinical Kidney Journal|December 11, 2025
Tolvaptan in Autosomal Dominant Polycystic Kidney Disease (ADPKD): a multicenter real life Italian experienceLaura Econimo, Diego Toso, Giovambattista Capasso, et al.
Genetics Research|March 5, 2019
Discrepant molecular and clinical diagnoses in Beckwith-Wiedemann and Silver-Russell syndromesDeborah J G Mackay, Jet Bliek, Maria Paola Lombardi, et al.
European Journal of Medical Genetics|June 25, 2013
Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterationsChiara Migliore, Emmanouil Athanasakis, Sophie Dahoun, et al.
Kidney International|June 19, 2009
Renal outcome in patients with congenital anomalies of the kidney and urinary tractSimone Sanna-Cherchi, Pietro Ravani, Valentina Corbani, et al.
Kidney International|January 13, 2012
Urinary secretion and extracellular aggregation of mutant uromodulin isoformsCéline Schaeffer, Angela Cattaneo, Matteo Trudu, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|April 28, 2012
[Mutant uromodulin is secreted in the urine of patients with familial hyperuricemic nephropathy and induces the formation of extracellular aggregates]Céline Schaeffer, Angela Cattaneo, Matteo Trudu, et al.
Italian Journal of Pediatrics|November 17, 2018
A new case report of severe mucopolysaccharidosis type VII: diagnosis, treatment with haematopoietic cell transplantation and prenatal diagnosis in a second pregnancyFrancesca Furlan, Attilio Rovelli, Miriam Rigoldi, et al.
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