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Roser Torra

Showing results (21-30 of 161) with videos related to

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Clinical Kidney Journal|June 12, 2015
Hypertension in autosomal-dominant polycystic kidney disease (ADPKD)Laia Sans-Atxer, Roser Torra, Patricia Fernández-Llama
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 12, 2025
Evolving strategies for early diagnosis, proactive prevention and treatment of CKDAlberto Ortiz, Motoko Yanagita, Hideki Yokoi, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 29, 2004
Collagen type IV (alpha3-alpha4) nephropathy: from isolated haematuria to renal failureRoser Torra, Bárbara Tazón-Vega, Elisabet Ars, et al.
Medicina Clinica|October 12, 2007
[Sodium transporters and aquaporins: future renal biomarkers?]Cristina Esteva-Font, Roser Torra Balcells, Patricia Fernández-Llama
Clinical Kidney Journal|December 4, 2023
Why do we keep ignoring sex in kidney disease?Magdalena Jankowska, María José Soler, Kate I Stevens, et al.
Clinical Kidney Journal|December 12, 2017
Recommendations for imaging-based diagnosis and management of renal angiomyolipoma associated with tuberous sclerosis complexMaría José Buj Pradilla, Teresa Martí Ballesté, Roser Torra, et al.
Lancet (London, England)|March 2, 2026
Autosomal dominant polycystic kidney diseaseAlbert C M Ong, Sol Carriazo, Becky Mingyao Ma, et al.
Nefrologia|September 26, 2025
Phenotypic variability in cystinosis: Lessons from an atypical caseDiego Toso, Monica Furlano, Adria Tinoco, et al.
Molecular Genetics & Genomic Medicine|October 22, 2014
Diagnosis of autosomal dominant polycystic kidney disease using efficient PKD1 and PKD2 targeted next-generation sequencingDaniel Trujillano, Gemma Bullich, Stephan Ossowski, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|October 29, 2003
Autosomal recessive Alport's syndrome and benign familial hematuria are collagen type IV diseasesBárbara Tazón Vega, Cèlia Badenas, Elisabet Ars, et al.
Pageof 17

Showing results (21-30 of 161) with videos related to

Sort By:
Pageof 17
Clinical Kidney Journal|June 12, 2015
Hypertension in autosomal-dominant polycystic kidney disease (ADPKD)Laia Sans-Atxer, Roser Torra, Patricia Fernández-Llama
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 12, 2025
Evolving strategies for early diagnosis, proactive prevention and treatment of CKDAlberto Ortiz, Motoko Yanagita, Hideki Yokoi, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 29, 2004
Collagen type IV (alpha3-alpha4) nephropathy: from isolated haematuria to renal failureRoser Torra, Bárbara Tazón-Vega, Elisabet Ars, et al.
Medicina Clinica|October 12, 2007
[Sodium transporters and aquaporins: future renal biomarkers?]Cristina Esteva-Font, Roser Torra Balcells, Patricia Fernández-Llama
Clinical Kidney Journal|December 4, 2023
Why do we keep ignoring sex in kidney disease?Magdalena Jankowska, María José Soler, Kate I Stevens, et al.
Clinical Kidney Journal|December 12, 2017
Recommendations for imaging-based diagnosis and management of renal angiomyolipoma associated with tuberous sclerosis complexMaría José Buj Pradilla, Teresa Martí Ballesté, Roser Torra, et al.
Lancet (London, England)|March 2, 2026
Autosomal dominant polycystic kidney diseaseAlbert C M Ong, Sol Carriazo, Becky Mingyao Ma, et al.
Nefrologia|September 26, 2025
Phenotypic variability in cystinosis: Lessons from an atypical caseDiego Toso, Monica Furlano, Adria Tinoco, et al.
Molecular Genetics & Genomic Medicine|October 22, 2014
Diagnosis of autosomal dominant polycystic kidney disease using efficient PKD1 and PKD2 targeted next-generation sequencingDaniel Trujillano, Gemma Bullich, Stephan Ossowski, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|October 29, 2003
Autosomal recessive Alport's syndrome and benign familial hematuria are collagen type IV diseasesBárbara Tazón Vega, Cèlia Badenas, Elisabet Ars, et al.
Pageof 17