Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Roser Torra

Showing results (41-50 of 161) with videos related to

Pageof 17
Sort By:
Nefrologia|January 26, 2024
Correlation of X chromosome inactivation with clinical presentation of Fabry disease in a case reportPablo Rodríguez Doyágüez, Mónica Furlano, Elisabet Ars Criach, et al.
The Lancet Regional Health. Europe|June 23, 2025
A call for urgent action on chronic kidney disease across EuropeCharles J Ferro, Christoph Wanner, Valerie Luyckx, et al.
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia|June 2, 2011
Effects of rapamycin on angiomyolipomas in patients with tuberous sclerosisCristina Cabrera López, Teresa Martí, Violeta Catalá, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|July 31, 2007
Genetic testing for X-linked Alport syndrome by direct sequencing of COL4A5 cDNA from hair root RNA samplesBárbara Tazón-Vega, Elisabet Ars, Moisès Burset, et al.
BMC Nephrology|September 7, 2013
Renal replacement therapy in ADPKD patients: a 25-year survey based on the Catalan registryVíctor Martínez, Jordi Comas, Emma Arcos, et al.
Journal of Medical Genetics|September 2, 2025
Long-term efficacy of migalastat in females with Fabry diseaseStaci Kallish, Antonia Camporeale, Robert J Hopkin, et al.
BMC Nephrology|April 13, 2019
Novel homozygous OSGEP gene pathogenic variants in two unrelated patients with Galloway-Mowat syndrome: case report and review of the literatureAndrea Domingo-Gallego, Mónica Furlano, Marc Pybus, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 21, 2011
Acute renal failure associated to paroxysmal nocturnal haemoglobinuria leads to intratubular haemosiderin accumulation and CD163 expressionJosé Ballarín, Yolanda Arce, Roser Torra Balcells, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 29, 2014
Spanish guidelines for the management of autosomal dominant polycystic kidney diseaseElisabet Ars, Carmen Bernis, Gloria Fraga, et al.
Clinical Kidney Journal|May 2, 2022
Comparative analysis of tools to predict rapid progression in autosomal dominant polycystic kidney diseaseJavier Naranjo, Mónica Furlano, Ferran Torres, et al.
Pageof 17

Showing results (41-50 of 161) with videos related to

Sort By:
Pageof 17
Nefrologia|January 26, 2024
Correlation of X chromosome inactivation with clinical presentation of Fabry disease in a case reportPablo Rodríguez Doyágüez, Mónica Furlano, Elisabet Ars Criach, et al.
The Lancet Regional Health. Europe|June 23, 2025
A call for urgent action on chronic kidney disease across EuropeCharles J Ferro, Christoph Wanner, Valerie Luyckx, et al.
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia|June 2, 2011
Effects of rapamycin on angiomyolipomas in patients with tuberous sclerosisCristina Cabrera López, Teresa Martí, Violeta Catalá, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|July 31, 2007
Genetic testing for X-linked Alport syndrome by direct sequencing of COL4A5 cDNA from hair root RNA samplesBárbara Tazón-Vega, Elisabet Ars, Moisès Burset, et al.
BMC Nephrology|September 7, 2013
Renal replacement therapy in ADPKD patients: a 25-year survey based on the Catalan registryVíctor Martínez, Jordi Comas, Emma Arcos, et al.
Journal of Medical Genetics|September 2, 2025
Long-term efficacy of migalastat in females with Fabry diseaseStaci Kallish, Antonia Camporeale, Robert J Hopkin, et al.
BMC Nephrology|April 13, 2019
Novel homozygous OSGEP gene pathogenic variants in two unrelated patients with Galloway-Mowat syndrome: case report and review of the literatureAndrea Domingo-Gallego, Mónica Furlano, Marc Pybus, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 21, 2011
Acute renal failure associated to paroxysmal nocturnal haemoglobinuria leads to intratubular haemosiderin accumulation and CD163 expressionJosé Ballarín, Yolanda Arce, Roser Torra Balcells, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 29, 2014
Spanish guidelines for the management of autosomal dominant polycystic kidney diseaseElisabet Ars, Carmen Bernis, Gloria Fraga, et al.
Clinical Kidney Journal|May 2, 2022
Comparative analysis of tools to predict rapid progression in autosomal dominant polycystic kidney diseaseJavier Naranjo, Mónica Furlano, Ferran Torres, et al.
Pageof 17