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Claudia Izzi

Showing results (11-20 of 80) with videos related to

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American Journal of Medical Genetics|March 29, 2002
Sequencing of the GRIK1 gene in patients with juvenile absence epilepsy does not reveal mutations affecting receptor structureClaudia Izzi, Alessandro Barbon, Rebekka Kretz, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|August 19, 2020
[The complex etiopathogenesis of focal segmental glomerulosclerosis]Martina Tedesco, Elisa Delbarba, Claudia Izzi, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|October 29, 2021
[ADPKD and intracranial aneurysms: indications for screening, follow-up and clinical management]Laura Econimo, Letizia Zeni, Roberta Cortinovis, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|October 6, 2010
[Genetics and nosological classification of renal cystic diseases]Claudia Izzi, Laura Sottini, Nadia Dallera, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|April 13, 2016
[Genetics and genetic counseling]Claudia Izzi, Francesca Liut, Nadia Dallera, et al.
Kidney International|October 1, 2014
The Case | Cystic renal disease, nephrogenic diabetes insipidus, and polycytemiaClaudia Izzi, Nadia Dallera, Chiara Manenti, et al.
Skeletal Radiology|May 27, 2014
Thanatophoric dysplasia. Correlation among bone X-ray morphometry, histopathology, and gene analysisUgo E Pazzaglia, Carla M Donzelli, Claudia Izzi, et al.
Disease Models & Mechanisms|June 7, 2023
Leader peptide or pro-segment mutants of renin are misrouted to mitochondria in autosomal dominant tubulointerstitial kidney diseaseCéline Schaeffer, Maurizio De Fusco, Elena Pasqualetto, et al.
Kidney International Reports|December 19, 2022
Autosomal Dominant Tubulointerstitial Kidney Disease: An Emerging Cause of Genetic CKDLaura Econimo, Celine Schaeffer, Letizia Zeni, et al.
Kidney International|March 2, 2011
The Case ∣ Familial occurrence of retinitis pigmentosa, deafness, and nephropathyClaudia Izzi, Pietro Maffei, Gabriella Milan, et al.
Pageof 8

Showing results (11-20 of 80) with videos related to

Sort By:
Pageof 8
American Journal of Medical Genetics|March 29, 2002
Sequencing of the GRIK1 gene in patients with juvenile absence epilepsy does not reveal mutations affecting receptor structureClaudia Izzi, Alessandro Barbon, Rebekka Kretz, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|August 19, 2020
[The complex etiopathogenesis of focal segmental glomerulosclerosis]Martina Tedesco, Elisa Delbarba, Claudia Izzi, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|October 29, 2021
[ADPKD and intracranial aneurysms: indications for screening, follow-up and clinical management]Laura Econimo, Letizia Zeni, Roberta Cortinovis, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|October 6, 2010
[Genetics and nosological classification of renal cystic diseases]Claudia Izzi, Laura Sottini, Nadia Dallera, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|April 13, 2016
[Genetics and genetic counseling]Claudia Izzi, Francesca Liut, Nadia Dallera, et al.
Kidney International|October 1, 2014
The Case | Cystic renal disease, nephrogenic diabetes insipidus, and polycytemiaClaudia Izzi, Nadia Dallera, Chiara Manenti, et al.
Skeletal Radiology|May 27, 2014
Thanatophoric dysplasia. Correlation among bone X-ray morphometry, histopathology, and gene analysisUgo E Pazzaglia, Carla M Donzelli, Claudia Izzi, et al.
Disease Models & Mechanisms|June 7, 2023
Leader peptide or pro-segment mutants of renin are misrouted to mitochondria in autosomal dominant tubulointerstitial kidney diseaseCéline Schaeffer, Maurizio De Fusco, Elena Pasqualetto, et al.
Kidney International Reports|December 19, 2022
Autosomal Dominant Tubulointerstitial Kidney Disease: An Emerging Cause of Genetic CKDLaura Econimo, Celine Schaeffer, Letizia Zeni, et al.
Kidney International|March 2, 2011
The Case ∣ Familial occurrence of retinitis pigmentosa, deafness, and nephropathyClaudia Izzi, Pietro Maffei, Gabriella Milan, et al.
Pageof 8