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Francesco Emma

Showing results (151-160 of 225) with videos related to

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Human Molecular Genetics|October 27, 2022
Genistein improves renal disease in a mouse model of nephropathic cystinosis: a comparison study with cysteamineEster De Leo, Anna Taranta, Roberto Raso, et al.
Nature Reviews. Nephrology|October 22, 2024
International expert consensus statement on the diagnosis and management of congenital nephrogenic diabetes insipidus (arginine vasopressin resistance)Elena Levtchenko, Gema Ariceta, Olga Arguedas Flores, 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.
Italian Journal of Pediatrics|April 22, 2017
The Italian Society for Pediatric Nephrology (SINePe) consensus document on the management of nephrotic syndrome in children: Part I - Diagnosis and treatment of the first episode and the first relapseAndrea Pasini, Elisa Benetti, Giovanni Conti, 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.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 11, 2006
Phenotypic and genetic heterogeneity in Dent's disease--the results of an Italian collaborative studyEnrica Tosetto, Gian Marco Ghiggeri, Francesco Emma, et al.
Kidney International|November 21, 2020
Updating the International IgA Nephropathy Prediction Tool for use in childrenSean J Barbour, Rosanna Coppo, Lee Er, et al.
BMC Medical Genetics|October 26, 2013
Detailed investigations of proximal tubular function in Imerslund-Gräsbeck syndromeTina Storm, Christina Zeitz, Olivier Cases, et al.
Clinical Journal of the American Society of Nephrology : CJASN|May 2, 2009
Clinical features and long-term outcome of nephrotic syndrome associated with heterozygous NPHS1 and NPHS2 mutationsGianluca Caridi, Maddalena Gigante, Pietro Ravani, et al.
JCI Insight|August 10, 2023
A phase I study of autologous mesenchymal stromal cells for severe steroid-dependent nephrotic syndromeMarina Vivarelli, Manuela Colucci, Mattia Algeri, et al.
Pageof 23

Showing results (151-160 of 225) with videos related to

Sort By:
Pageof 23
Human Molecular Genetics|October 27, 2022
Genistein improves renal disease in a mouse model of nephropathic cystinosis: a comparison study with cysteamineEster De Leo, Anna Taranta, Roberto Raso, et al.
Nature Reviews. Nephrology|October 22, 2024
International expert consensus statement on the diagnosis and management of congenital nephrogenic diabetes insipidus (arginine vasopressin resistance)Elena Levtchenko, Gema Ariceta, Olga Arguedas Flores, 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.
Italian Journal of Pediatrics|April 22, 2017
The Italian Society for Pediatric Nephrology (SINePe) consensus document on the management of nephrotic syndrome in children: Part I - Diagnosis and treatment of the first episode and the first relapseAndrea Pasini, Elisa Benetti, Giovanni Conti, 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.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 11, 2006
Phenotypic and genetic heterogeneity in Dent's disease--the results of an Italian collaborative studyEnrica Tosetto, Gian Marco Ghiggeri, Francesco Emma, et al.
Kidney International|November 21, 2020
Updating the International IgA Nephropathy Prediction Tool for use in childrenSean J Barbour, Rosanna Coppo, Lee Er, et al.
BMC Medical Genetics|October 26, 2013
Detailed investigations of proximal tubular function in Imerslund-Gräsbeck syndromeTina Storm, Christina Zeitz, Olivier Cases, et al.
Clinical Journal of the American Society of Nephrology : CJASN|May 2, 2009
Clinical features and long-term outcome of nephrotic syndrome associated with heterozygous NPHS1 and NPHS2 mutationsGianluca Caridi, Maddalena Gigante, Pietro Ravani, et al.
JCI Insight|August 10, 2023
A phase I study of autologous mesenchymal stromal cells for severe steroid-dependent nephrotic syndromeMarina Vivarelli, Manuela Colucci, Mattia Algeri, et al.
Pageof 23