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Francesco Emma

Showing results (161-170 of 225) with videos related to

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Kidney International|August 2, 2024
Application of the updated International IgA Nephropathy Prediction Tool in children one or two years post-biopsySean J Barbour, Rosanna Coppo, Lee Er, et al.
The Journal of Pediatrics|July 26, 2011
Cysteamine toxicity in patients with cystinosisMartine T P Besouw, Richard Bowker, Jean-Paul Dutertre, et al.
Pediatric Nephrology (Berlin, Germany)|November 26, 2024
C3 glomerulopathy in children: a European longitudinal study evaluating outcomeAndrea Cappoli, Tanja Kersnik-Levart, Valeria Silecchia, et al.
The Journal of Pediatrics|May 9, 2013
Copper deficiency in patients with cystinosis with cysteamine toxicityMartine T P Besouw, Jerry Schneider, Mirian C Janssen, et al.
Journal of the American Society of Nephrology : JASN|July 12, 2024
Ketogenic Diet and Progression of Kidney Disease in Animal Models of Nephropathic CystinosisFrancesco Bellomo, Sara Pugliese, Sara Cairoli, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 27, 2008
Genetic risk factors in typical haemolytic uraemic syndromeAnna Taranta, Alessandra Gianviti, Alessia Palma, et al.
American Journal of Physiology. Renal Physiology|October 26, 2020
Beyond the tubule: pathological variants of <i>LRP2</i>, encoding the megalin receptor, result in glomerular loss and early progressive chronic kidney diseaseJennifer R Charlton, Weizhen Tan, Ghaleb Daouk, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 29, 2021
Distal renal tubular acidosis: ERKNet/ESPN clinical practice pointsFrancesco Trepiccione, Steven B Walsh, Gema Ariceta, et al.
American Journal of Human Genetics|May 25, 2010
Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 geneJoanna Walczak-Sztulpa, Jonathan Eggenschwiler, Daniel Osborn, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 8, 2018
Impaired urinary concentration ability is a sensitive predictor of renal disease progression in Joubert syndromeSara Nuovo, Laura Fuiano, Alessia Micalizzi, et al.
Pageof 23

Showing results (161-170 of 225) with videos related to

Sort By:
Pageof 23
Kidney International|August 2, 2024
Application of the updated International IgA Nephropathy Prediction Tool in children one or two years post-biopsySean J Barbour, Rosanna Coppo, Lee Er, et al.
The Journal of Pediatrics|July 26, 2011
Cysteamine toxicity in patients with cystinosisMartine T P Besouw, Richard Bowker, Jean-Paul Dutertre, et al.
Pediatric Nephrology (Berlin, Germany)|November 26, 2024
C3 glomerulopathy in children: a European longitudinal study evaluating outcomeAndrea Cappoli, Tanja Kersnik-Levart, Valeria Silecchia, et al.
The Journal of Pediatrics|May 9, 2013
Copper deficiency in patients with cystinosis with cysteamine toxicityMartine T P Besouw, Jerry Schneider, Mirian C Janssen, et al.
Journal of the American Society of Nephrology : JASN|July 12, 2024
Ketogenic Diet and Progression of Kidney Disease in Animal Models of Nephropathic CystinosisFrancesco Bellomo, Sara Pugliese, Sara Cairoli, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 27, 2008
Genetic risk factors in typical haemolytic uraemic syndromeAnna Taranta, Alessandra Gianviti, Alessia Palma, et al.
American Journal of Physiology. Renal Physiology|October 26, 2020
Beyond the tubule: pathological variants of <i>LRP2</i>, encoding the megalin receptor, result in glomerular loss and early progressive chronic kidney diseaseJennifer R Charlton, Weizhen Tan, Ghaleb Daouk, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 29, 2021
Distal renal tubular acidosis: ERKNet/ESPN clinical practice pointsFrancesco Trepiccione, Steven B Walsh, Gema Ariceta, et al.
American Journal of Human Genetics|May 25, 2010
Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 geneJoanna Walczak-Sztulpa, Jonathan Eggenschwiler, Daniel Osborn, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 8, 2018
Impaired urinary concentration ability is a sensitive predictor of renal disease progression in Joubert syndromeSara Nuovo, Laura Fuiano, Alessia Micalizzi, et al.
Pageof 23